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Iscia Teresinha Lopes Cendes

Dados pessoais

  • HS Health Sciences
  • LS Life Sciences
  • MU Multidisciplinary
  • PS Physical Sciences
  • SH Social Sciences & Humanities
# Nome Links Grande Área Área
1 Americo Ceiki SAKAMOTO Ciências da Saúde Medicina
2 Antonio Lucio Teixeira JUNIOR Ciências da Saúde Medicina
3 Benito Pereira DAMASCENO Ciências da Saúde Medicina
4 Carlos Eduardo STEINER Ciências Biológicas Genética
5 Carlos Roberto De Mello RIEDER Ciências da Saúde Medicina
6 Celso Darío RAMOS Ciências da Saúde Medicina
7 Clarissa De Rosalmeida DANTAS Ciências da Saúde Medicina
8 Cláudio Eduardo Muller BANZATO Ciências da Saúde Medicina
9 Dagma Venturini Marques ABRAMIDES Ciências Humanas Psicologia
10 Elza Márcia Targas YACUBIAN Ciências da Saúde Medicina
11 Esper Abrao CAVALHEIRO CpE Ciências Biológicas Fisiologia
12 Fernando CENDES Ciências da Saúde Medicina
13 Fernando Mazzilli LOUZADA CpE Ciências Humanas Psicologia
14 Francisco Eduardo Costa CARDOSO Ciências da Saúde Medicina
15 Jaderson Costa Da COSTA CpE Ciências da Saúde Medicina
16 Juan Clinton Llerena JUNIOR Ciências da Saúde Medicina
17 Laura Maria De Figueiredo Ferreira GUILHOTO Ciências da Saúde Medicina
18 Li Li MIN Ciências da Saúde Medicina
19 Lineu Cesar WERNECK Ciências da Saúde Medicina
20 Marcio Flavio Dutra MORAES CpE Ciências Biológicas Fisiologia
21 Maria Aparecida Camargos BICALHO Ciências da Saúde Medicina
22 Mauro MUSZKAT Ciências da Saúde Medicina
23 Mônica Barbosa De MELO Ciências Biológicas Genética
24 Orestes Vicente FORLENZA Ciências da Saúde Medicina
25 Paulo CARAMELLI Ciências da Saúde Medicina
26 Paulo DALGALARRONDO Ciências da Saúde Medicina
27 Ricardo Mario ARIDA CpE Ciências Biológicas Fisiologia
28 Salmo RASKIN Ciências da Saúde Medicina
29 Simone Rocha De Vasconcellos HAGE Ciências da Saúde Fonoaudiologia
30 Vera Lúcia Gil Da Silva LOPES Ciências Biológicas Genética
Figura 1. Número de publicações por ano e por tipo, considerando todas as publicações.
  1. Life Sciences Pharmacology
    Maria Carolina Pedro ATHIE; Fernando CENDES; Iscia Teresinha Lopes CENDES; André Schwambach VIEIRA. 2022. 'unraveling the molecular mechanisms underlying parasite-host interaction in taenia solium neurocysticercosis'. In: Xiii semana de pesquisa da fcm. Brasil.
  2. Life Sciences Neuroscience (miscellaneous)
    Avansini Simoni H; F PUPPO; J ADAMS; Vieira Andre S; Coan A C et al. 2022. In vitro human model of focal cortical dysplasia demonstrates early junctional instability in the neuroepithelium and network hyperexcitability. In: 14th european epilepsy congress. Suiça.
  3. Health Sciences Neurology (clinical)
    Mejía Granados Diana MARCELA; Kawasaki De Araujo TÂNIA; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Alvim Marina K M; Yassuda Clarissa L et al. 2022. Characterization of the gut microbiome in patients with different forms of epilepsy and autoimmune encephalitis. In: 8th brainn congress. Brasil.
  4. Health Sciences Medicine (miscellaneous)
    Danielle Carmo Ferreira BRUNO; M MARTIN; Simoni Helena AVANSINI; Alvim Marina K M; Fernando CENDES et al. 2022. Circulating nucleic acids as a potential non-invasive biomarker for predicting pharmacoresistant in patients with mesial temporal lobe epilepsy. In: 8th brainn congress. Brasil.
  5. Life Sciences Neurology
    Maria Luiza BENEVIDES; Moraes Helena Tadiello DE; Mejía Granados Diana MARCELA; Bonadia Luciana CARDOSO; Leticia SAUMA et al. 2022. Clinical predictors of positive genetic investigation in developmental and epileptic encephalopathies. In: 8th brainn congress. Brasil.
  6. Life Sciences Genetics
    Moraes Helena Tadiello DE; Thais Crippa De OLIVEIRA; Bonadia Luciana CARDOSO; Mejía Granados Diana MARCELA; Maria Luiza BENEVIDES et al. 2022. Genetic characterization of a large cohort of patients with developmental and epileptic encephalopathies from latin america. In: 8th brainn congress. Brasil.
  7. Health Sciences Medicine (miscellaneous)
    Geraldis Jaqueline C; Danielle Carmo Ferreira BRUNO; De Souza WELLITON; Canto Amanda Morato DO; Alvim Marina K M et al. 2022. Genomic distribution of dna methylation in mesial temporal lobe epilepsy. In: 8th brainn congress. Brasil.
  8. Health Sciences Medicine (miscellaneous)
    Donatti AMANDA; Da Rosa Douglas C; F S OLIVEIRA; M QUINTERO; Y YAN et al. 2022. Multiomics analysis in the plasma of patients in chronic phase of ischemic stroke: insights into molecular mechanisms leading to recovery. In: 8th brainn congress. Brasil.
  9. Life Sciences Neuroscience (miscellaneous)
    Godoi Alexandre Barcia DE; Canto Amanda Morato DO; Donatti AMANDA; Da Rosa Douglas C; Alvim Marina K M et al. 2022. Searching for biomarkers of drug resistance in mesial temporal lobe epilepsy using ¹h-nmr spectroscopy. In: 8th brainn congress. Brasil.
  10. Life Sciences Neuroscience (miscellaneous)
    Geraldis Jaqueline C; Veiga Diogo F T; Danielle Carmo Ferreira BRUNO; Alvim Marina K M; Fábio ROGÉRIO et al. 2022. The role of genomic footprint in the mechanisms underlying mesial temporal lobe epilepsy: a single-cell approach. In: 8th brainn congress. Brasil.
  11. Health Sciences Neurology (clinical)
    Bruxel Estela M; Canto Amanda M; Alexandre Barcia De GODOI; De Souza WELLITON; Yasuda C L et al. 2022. The transcriptome of mesial temporal lobe epilepsy with hippocampal sclerosis. In: 8th brainn congress. Brasil.
  12. Life Sciences Animal Science and Zoology
    Athié M C P; Fernando CENDES; Iscia Teresinha Lopes CENDES; Andre Schwambach VIEIRA. 2022. Unraveling the molecular mechanisms underlying parasite-host interaction in taenia solium neurocysticercosis. In: 8th brainn congress. Brasil.
  13. Physical Sciences Computer Science Applications
    Thais Crippa De OLIVEIRA; De Souza WELLITON; Cristiane De Souza ROCHA; Benilton De Sá CARVALHO; Iscia Teresinha Lopes CENDES. 2022. Constructing new and improved platform for data sharing in the brazilian initiative on precision medicine (bipmed). In: 8th brainn congress. Brasil.
  14. Health Sciences Neurology (clinical)
    Pedro Henrique MAGALHÃES; Bruxel Estela M; Athié M C P; Alvim Marina K M; Secolin RODRIGO et al. 2022. An in-depth look at candidate loci for mesial temporal lobe epilepsy. In: 8th brainn congress. Brasil.
  15. Health Sciences Medicine (miscellaneous)
    Alexandre Barcia De GODOI; Canto Amanda M; Donatti AMANDA; Da Rosa Douglas C; Melissa Quintero ESCOBAR et al. 2020. Abordagem metabolômica na busca por biomarcadores de farmacorresistência em pacientes com epilepsia do lobo temporal mesial através de rmn de h¹. In: Xvi jornada brasileira de ressonância magnética. Brasil.
  16. Health Sciences Medicine (miscellaneous)
    Da Rosa Douglas C; Donatti AMANDA; Fabiana Dos Santos OLIVEIRA; Godoi Alexandre B; Canto Amanda M et al. 2020. Estudo metabolômico em plasma de pacientes com acidente vascular cerebral isquêmico através de 1h-rmn. In: Xvi jornada brasileira de ressonância magnética. Brasil.
  17. Health Sciences Neurology (clinical)
    Renata BARBOSA; Alexandre Hilário Berenguer De MATOS; Brunno CAMPOS; Casseb Raphael F; Pimentel Silva Luciana R et al. 2016. Brain proton magnetic resonance spectroscopy and t2-weighted in the pilocarpine model of temporal lobe epilepsy: changes after status epilepticus in rats. In: 46th annual meeting of the society for neuroscience. Estados Unidos.
  18. Health Sciences Medicine (miscellaneous)
    Beatriz Pereira De Sousa LIMA; Avansini Simoni H; Secolin RODRIGO; M L SANTOS; Coan Ana CAROLINA et al. 2015. Is it possible to identify patients with refractory epilepsy using a plasma-based test?. In: 2nd congress cepid brainn. Brasil.
  19. Health Sciences General Medicine
    C V L TEIXEIRA; T N C MAGALHÃES; Jessica E VICENTINI; Marina WEILER; Secolin RODRIGO et al. 2015. Tnf-α serum in mild cognitive impairment elderly - apoe epsilon 4 carriers versus non carriers. In: 2nd congresso cepid brainn. Brasil.
  20. Health Sciences Medicine (miscellaneous)
    Murilo G BORGES; Cristiane De Souza ROCHA; Benilton De Sá CARVALHO; Iscia Teresinha Lopes CENDES. 2015. Whole exome sequencing depth varies among samples with different ethnic background. In: 2nd congress cepid brainn. Brasil.
  21. Life Sciences Neuroscience (miscellaneous)
    M MAZUTTI; Torres Fabio R; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Simoni Helena AVANSINI; Secolin RODRIGO et al. 2015. Molecular studies of mtor and tau pathways in focal cortical dysplasia. In: 2nd congress cepid brainn. Brasil.
  22. Life Sciences Neuroscience (miscellaneous)
    Renata BARBOSA; André Schwambach VIEIRA; Alexandre Hilário Berenguer De MATOS; Brunno Machado De CAMPOS; Casseb Raphael F et al. 2015. Hippocampal volume and t2 signal changes in the pilocarpine model of temporal lobe epilepsy (poster; neuroscience 2015). In: Annual meeting of the society of neuroscience - neuroscience 2015. Estados Unidos.
  23. Health Sciences Medicine (miscellaneous)
    Joana PROTA; Rejane Scolari Resende PAIVA; Antonia Paula Marques De FARIA; Iscia Teresinha Lopes CENDES. 2015. Incidental findings of genomic testing: what patients want to know?. In: 2nd congress cepid brainn. Brasil.
  24. Health Sciences Neurology (clinical)
    Secolin RODRIGO; Patrícia Aline O RIBEIRO; Fabio Rossi TORRES; Murilo G BORGES; Coan A C et al. 2014. Gene-variants associated with familial mesial temporal lobe epilepsy identified by whole exome sequencing. In: 64th annual meeting of the american society of human genetics. Brasil.
  25. Life Sciences Genetics
    Alexandre Hilário Berenguer MATOS; André S VIEIRA; Pascoal V D B; Cristiane De Souza ROCHA; M F D MORAES et al. 2014. Evidence pointing to abnormal energy metabolism in two genetic animal models of epilepsy. In: 64th annual meeting of the american society of human genetics. Brasil.
  26. Life Sciences Neuroscience (miscellaneous)
    M MAZUTTI; Patrícia Aline O RIBEIRO; Avansini Simoni H; Secolin RODRIGO; Benilton De Sá CARVALHO et al. 2014. Molecular studies of mtor and tau pathways in focal cortical dysplasia. In: 64th annual meeting of the american society of human genetics. Brasil.
  27. Social Sciences & Humanities Psychology (miscellaneous)
    Murilo G BORGES; Cristiane De Souza ROCHA; Benilton De Sá CARVALHO; Iscia Teresinha Lopes CENDES. 2014. Comparisons on whole exome capturing homogeneity among diferent versions of capturing kits and populations. In: 64th annual meeting of the american society of human genetics. Brasil.
  28. Health Sciences Neurology (clinical)
    Benilton De Sá CARVALHO; Alexandre Hilário Berenguer MATOS; André Schwambach VIEIRA; Iscia Teresinha Lopes CENDES. 2014. Developing a new aproach to transcriptomic characterization of mesial temporal lobe epilepsy models through next-generation sequencing. In: 64th annual meeting of the american society of human genetics. Brasil.
  29. Life Sciences Genetics
    W SOUZA; Benilton De Sá CARVALHO; Dogini Danyella B; Iscia Teresinha Lopes CENDES. 2014. Identification of diferentialy methylated genes potentialy associated with neurological diseases. In: 64th annual meeting of the american society of human genetics. Brasil.
  30. Life Sciences Neuroscience (miscellaneous)
    Jaira F De VASCONCELLOS; Maurer Morelli Cláudia VIANNA; Cristiane De Souza ROCHA; Clarissa Lin YASUDA; Helder TEDESCHI et al. 2012. A gene expression-based in silico approach identifies new biological targets in human mesial temporal lobe epilepsy (poster; 64th annual meeting of american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  31. Health Sciences Cardiology and Cardiovascular Medicine
    Karen TAKAZAKI; Anelyssa Cysne Frota D ABREU; Iscia Teresinha Lopes CENDES; Anamarli NUCCI; Marcondes Cavalcante França JUNIOR. 2012. Spectral analysis of heart rate variability in sca 3 (poster; 64th annual meeting of the american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  32. Health Sciences Neurology (clinical)
    Marina Coelho GONSALVES; M C GONSALES; P M PRETO; Maria A MONTENEGRO; Marilisa Mantovani GUERREIRO et al. 2012. Applying multiple predictive algorithms to the molecular diagnosis of epilepsy (poster; 64th annual meeting of the american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  33. Health Sciences Neurology (clinical)
    Danyella Barbosa DOGINI; Anamarli NUCCI; Iscia Teresinha Lopes CENDES; Marcondes Cavalcante França JUNIOR. 2012. Expression profile of micrornas mir-9 and mir-206 in human amyotrophic lateral sclerosis (poster; 64th annual meeting of trhe american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  34. Life Sciences Neuroscience (miscellaneous)
    Simoni Helena AVANSINI; Fábio Rossi TORRES; Fábio ROGÉRIO; Danyella Barbosa DOGINI; Ana Carolina COAN et al. 2012. Investigating the role of micrornas regulation in the development of focal cortical dysplasia (poster; 64th annual meeting of the american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  35. Health Sciences Neurology (clinical)
    Alexandre Hilário Berenguer MATOS; Vinícius D B PASCOAL; Deborah NASCIMENTO; Cristiane De Souza ROCHA; Jaira F De VASCONCELLOS et al. 2012. Gene expression profile in genetic models of generalized epilepsy: clues into underlying mechanism (64th annual meeting of the american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  36. Health Sciences Neurology (clinical)
    Danyella Barbosa DOGINI; Cristiane De Souza ROCHA; Clarissa Lin YASUDA; Helder TEDESCHI; De Oliveira EVANDRO et al. 2012. Microrna expression profile in mesial temporal sclerosis provides insight into underlying mechanisms (poster; 64th annual meeting of american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  37. Health Sciences Neurology (clinical)
    Beatriz SILVA; Rachel P GUIMARÃES; Felipe P G BERGO; Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU et al. 2012. Mri t2-relaxometry in spinocerebellar ataxia type 3 (machado-joseph disease) (poster; 64th annual meeting of the american academy of neurolgy). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  38. Health Sciences Neurology (clinical)
    Cynthia SILVA; Anelyssa Cysne Frota D ABREU; Iscia Teresinha Lopes CENDES; Marcondes Cavalcante França JUNIOR. 2012. Survey of non-motors symptoms in patients with friedreich ataxia (poster; 64th annual meeting of the american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  39. Life Sciences Neurology
    Cynthia SILVA; Felipe P G BERGO; Anelyssa Cysne Frota D ABREU; Iscia Teresinha Lopes CENDES; Marcondes Cavalcante França JUNIOR. 2012. T2 relaxation time correlates with disease severity in friedreich's ataxia (poster; 64th annual meeting of the american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  40. Health Sciences Neurology (clinical)
    Luiza PIOVESANA; Lidiane Soares De CAMPOS; Fábio Rossi TORRES; Fernando CENDES; Iscia Teresinha Lopes CENDES et al. 2012. Multimodal neuroimaging study of the cerebellum in primary cervical dystonia (poster; 64th annual meeting of the american academy of neurology). In: 64th annual meeting of american academy of neurology. Estados Unidos.
  41. Life Sciences Neuroscience (miscellaneous)
    Danyella Barbosa DOGINI; Anamarli NUCCI; H M T De ANDRADE; Iscia Teresinha Lopes CENDES; Marcondes Cavalcante França JUNIOR. 2012. Microrna-9 and-206 expression profile in human amyotrophic lateral sclerosis (poster; xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  42. Life Sciences Animal Science and Zoology
    K A G TAKAZAKI; Anelyssa Cysne Frota D ABREU; Iscia Teresinha Lopes CENDES; Anamarli NUCCI; Marcondes Cavalcante França JUNIOR. 2012. Análise espectral da variabiliddae da frequência cardíaca na sca3 (poster; xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  43. Life Sciences Animal Science and Zoology
    Bruno SCHMID; Julio Cesar SOMAZZ; Castellano GABRIELA; Iscia Teresinha Lopes CENDES; Marcondes Cavalcante França JUNIOR. 2012. Espectroscopia de fósforo no músculo de pacientes com doença de machado-joseph (poster; xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  44. Life Sciences Neurology
    G F RAMOS; Danyella Barbosa DOGINI; C CARTAXO; H A G TEIVE; Jardim L B et al. 2012. Depressão na ataxia de friedreich: frequência e substrato anatômico (oral; xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  45. Health Sciences Neurology (clinical)
    M B NUNES; A R M MARTINEZ; Anelyssa Cysne Frota D ABREU; Iscia Teresinha Lopes CENDES; Marcondes Cavalcante França JUNIOR. 2012. Distonia na doença de machado-joseph: frequencia; aspectos clínicos e relação com sintomas não motores (oral; xxv congresso barsileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  46. Life Sciences Neurology
    G F RAMOS; Danyella Barbosa DOGINI; C CARTAXO; H A G TEIVE; L B JARDIM et al. 2012. Estudo de mutações no gene spg4 em pacientes brasileiros com paraparesia espástica hereditária (oral; xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  47. Health Sciences Radiology, Nuclear Medicine and Imaging
    A R M MARTINEZ; M B NUNES; Anamarli NUCCI; Iscia Teresinha Lopes CENDES; Anelyssa Cysne Frota D ABREU et al. 2012. Fadifa; sonolência diurna e depressão na doença de machado-joseph (xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  48. Life Sciences Neurology
    Chevis Camila F; Felipe P G BERGO; Silva Cynthia B; Iscia Teresinha Lopes CENDES; Marcondes Cavalcante França JUNIOR. 2012. Spinal cord atrophy has a distinctive pattern and correlates with disability in friedreich's ataxia (oral; xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  49. Health Sciences Neurology (clinical)
    M C A SANTOS; Luiza PIOVESANA; Lidiane Soares De CAMPOS; Iscia Teresinha Lopes CENDES; Fernando CENDES et al. 2012. Avaliação estrutural do cerebelo nas distonias craniocervicais primárias (oral; xxv congresso brasileiro de neurologia). In: Xxv congresso brasileiro de neurologia. Brasil.
  50. Life Sciences Neuroscience (miscellaneous)
    Alexandre Hilário Berenguer MATOS; Vinicius D Ávila Bittencourt PASCOAL; D R NASCIMENTO; Sarah MARTINS; Rocha Cristiane De SOUZA et al. 2012. A caracterização do perifl de expressão gênica em larga escala em modelos genéticos de epilepsia fornece elementos para entender os mecanismos envolvidos na epileptogênese em roedores (xxxiv congresso brasileiro de epilepsia). In: Xxxiv congresso brasileiro de epilepsia. Brasil.
  51. Life Sciences Genetics
    M C GONSALES; P M PRETO; Montenegro MA; Marilisa M GUERREIRO; Iscia Teresinha Lopes CENDES. 2012. Correlações entre o genótipo e o fenótipo na síndrome de dravet com mutações em scn1a aumentam a acurácia do diagnóstic molecular (xxxiv congresso brasileiro de epilepsia). In: Xxxiv congresso brasileiro de epilepsia. Brasil.
  52. Life Sciences Neurology
    Danyella Barbosa DOGINI; Simoni Helena AVANSINI; Fabio Rossi TORRES; Fábio ROGÉRIO; Rocha Cristiane De SOUZA et al. 2012. Microrna expression orifile in epilepsy: breaking molecular barriers (xxxiv congresso brasileiro de epilepsia). In: Xxxiv congresso brasileiro de epilepsia. Brasil.
  53. Health Sciences Radiology, Nuclear Medicine and Imaging
    Marcondes Cavalcante França JUNIOR; Rachel P GUIMARÃES; Clarissa Lin YASUDA; Anelyssa Cysne Frota D ABREU; Camila Miranda LOPES et al. 2011. Diffusion-tensor imaging shows diffuse white matter damage in spg11(poster; 63rd annual meeting of american academy of neurology). In: 63rd annual meeting of american academy of neurology. Estados Unidos.
  54. Life Sciences Neurology
    C F CHEVIS; Marcondes Cavalcante França JUNIOR; Felipe P G BERGO; Anelyssa Cysne Frota D ABREU; Rachel P GUIMARÃES et al. 2011. Distinct patterns of spinal cord atrophy in machado-joseph disease and friedreich's ataxia (poster; 63rd annual meeting of american academy of neurology). In: 63rd annual meeting of american academy of neurology. Estados Unidos.
  55. Life Sciences Neuroscience (miscellaneous)
    Rachel P GUIMARÃES; Clarissa Lin YASUDA; Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Iscia Teresinha Lopes CENDES et al. 2011. Diffusion tensor imaging (dti) and voxel based morphometry (vbm) analysis reveal white matter abnormalities in machado-joseph (mjd) disease (poster; 63rd annual meeting of american academy of neurology). In: 63rd annual meeting of american academy of neurology. Estados Unidos.
  56. Health Sciences Neurology (clinical)
    Luiz E G G BETTING; Li Li MIN; Iscia Teresinha Lopes CENDES; Marilisa Mantovani GUERREIRO; Carlos Alberto Mantovani GUERREIRO et al. 2011. Dti region of interest analysis of patients with idiopathic generalized epilepsy (poster; 63rd annual meeting of american academy of neurology). In: 63rd annual meeting of american academy of neurology. Estados Unidos.
  57. Health Sciences Neurology (clinical)
    Renato Oliveira SANTOS; Mariana Saragiotto Da SILVA; Rodrigo SECOLIN; Clarissa Lin YASUDA; Tonicarlo Rodrigues VELASCO et al. 2011. Association study shows relationship between mesial temporal lobe epilepsy with hippocampal sclerosis and ptprm gene ( poster; 63rd annual meeting of american academy of neurology). In: 63rd annual meeting of american academy of neurology. Estados Unidos.
  58. Health Sciences Neurology (clinical)
    Vinicius D Ávila Bittencourt PASCOAL; Marchesini Rafael BREGLIO; Tiago Campos PEREIRA; Gilioli ROVÍLSON; Jaqueline M MALHEIROS et al. 2010. Investigating the role of interleukin 1-beta in temporal lobe epilepsy in the pilocarpine rat model using rna interference (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  59. Health Sciences Neurology (clinical)
    Camila Miranda LOPES; Tiago Campos PEREIRA; Gilioli ROVÍLSON; Iscia Teresinha Lopes CENDES. 2010. Lithium reduces cell death in an in vitro model of machado-joseph disease (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  60. Life Sciences Neurology
    Marcondes Cavalcante França JUNIOR; Felipe P G BERGO; Anelyssa Cysne Frota D ABREU; Bonadia Luciana CARDOSO; Silva Marilza S et al. 2010. Spinal cord atrophy correlates with clinical disability in friedreich ataxia (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  61. Health Sciences Neurology (clinical)
    Danyella Barbosa DOGINI; Tiago Campos PEREIRA; Rocha Cristiane De SOUZA; Clarissa Lin YASUDA; Tedeschi HELDER et al. 2010. Changes in microrna expression profile in mesial temporal sclerosis (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  62. Health Sciences Radiology, Nuclear Medicine and Imaging
    M C GONSALES; P M PRETO; Marilisa Mantovani GUERREIRO; Iscia Teresinha Lopes CENDES. 2010. Using scn1a gene mutation screening in clinical practice (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  63. Health Sciences Neurology (clinical)
    Morita Márcia E; Luiz E G G BETTING; Clarissa Lin YASUDA; Maurer Morelli Cláudia VIANNA; Iscia Teresinha Lopes CENDES et al. 2010. Mri structural analysis of the hippocampus in families with mesial temporal lobe epilepsy (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  64. Life Sciences Neurology
    Luiz E G G BETTING; Morita Márcia E; Clarissa Lin YASUDA; Li Li MIN; Iscia Teresinha Lopes CENDES et al. 2010. Dti voxel-based analysis of patients with idiopathic generalized epilepsy (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  65. Health Sciences Neurology (clinical)
    R O SANTOS; Mariana Saragiotto Da SILVA; Rodrigo SECOLIN; Clarissa Lin YASUDA; Américo Ceike SAKAMOTO et al. 2010. Association of interleukin 1-beta and mesial temporal lobe epilepsy with hippocampal sclerosis (62nd annual meeting of the american academy of neurology). In: 62nd annual meeting of the american academy of neurology. Canadá.
  66. Life Sciences Neuroscience (miscellaneous)
    Vinicius D Ávila Bittencourt PASCOAL; Rafael B MARCHESINI; Alexandre Hilário Berenguer MATOS; Fábio Frangiotti CONTE; Pereira T C et al. 2010. The il 1beta have a protective action in the acute phase of the pilocarpine-induced epilepsy model (resumo expandido; xxxiii congresso da liga brasileira de epilepsia). In: Xxxiii congresso da liga brasileira de epilepsia. Estados Unidos.
  67. Health Sciences Neurology (clinical)
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Maurer Morelli Cláudia VIANNA; Bonadia Luciana CARDOSO; Marilza Santos SILVA et al. 2009. Length of the normal (cag) allele at mjd1 modulates age at onset in machado-joseph disease (61st annual meeting of the american aacademy of neurology 2009). In: 61st annual meeting of the american aacademy of neurology 2009. Portugal.
  68. Health Sciences Neurology (clinical)
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Yasuda Clarissa L; Mariana S A SOUZA; Iscia Teresinha Lopes CENDES et al. 2009. Thalamic volume reduction in machado-joseph disease (61st annual meeting of the american aacademy of neurology 2009). In: 61st annual meeting of the american aacademy of neurology 2009. Portugal.
  69. Life Sciences Neuroscience (miscellaneous)
    Yasuda Clarissa L; M E MORITA; Amanada R PEREIRA; Alessio ANDRÉIA; Luís E G G BETTING et al. 2009. Voxel-based morphometry reveals differences in familial and sporadic forms of refractory mtle (61st annual meeting of the american aacademy of neurology 2009). In: 61st annual meeting of the american aacademy of neurology 2009. Portugal.
  70. Health Sciences Neurology (clinical)
    Maurer Morelli Cláudia VIANNA; Cristiane De Souza ROCHA; Romenia Ramos DOMINGUES; Helder TEDESCHI; Evandro P L De OLIVEIRA et al. 2009. Gene expression profile in familial and sporadic forms of mesial tempotal lobe epilepsy (61st annual meeting of the american academy of neurology 2009). In: 61st annual meeting of the american academy of neurology 2009. Portugal.
  71. Life Sciences Neuroscience (miscellaneous)
    Marchesini Rafael BREGLIO; Vnícius D Avila Bittencourt PASCOAL; Tiago Campos PEREIRA; Rovilson GILIOLI; Iscia Teresinha Lopes CENDES. 2009. Transvascular delivery of sirnas into the rat brain (61st annual meeting of the american aacademy of neurology 2009). In: 61st annual meeting of the american aacademy of neurology 2009. Portugal.
  72. Life Sciences Neuroscience (miscellaneous)
    Marcelo Jun MURAI; Sassonia R; M G De OLIVEIRA; Iscia Teresinha Lopes CENDES. 2009. Characterization of the interaction between c-terminal half of human juvenile myoclonic epilepsy protein efhc1 and ca2+ and mg2+ ions (lnls activity report 2008). In: Lnls activity report 2008. Brasil.
  73. Health Sciences Neurology (clinical)
    Cláudia V Maurer MORELLI; Rocha Cristiane De SOUZA; Romenia Ramos DOMINGUES; Clarissa Lin YASUDA; Helder TEDESCHI et al. 2009. Gene expression profile suggests a different molecular mechanism for familial and sporadic forms of mesial temporal lobe epilepsy (aes 63rd annual meeting of the american epilepsy society 2009). In: Aes 63rd annual meeting of the american epilepsy society 2009. Estados Unidos.
  74. Health Sciences Neurology (clinical)
    Danyella Barbosa DOGINI; Tiago Campos PEREIRA; Cristiane De Souza ROCHA; Clarissa Lin YASUDA; Helder TEDESCHI et al. 2009. Evidence of microrna regulation in mesial temporal sclerosis (aes 63rd annual meeting of the american epilepsy society 2009). In: Aes 63rd annual meeting of the american epilepsy society 2009. Estados Unidos.
  75. Health Sciences Neurology (clinical)
    Angela Cristina Do VALLE; Cláudia V Maurer MORELLI; Cristiane De Souza ROCHA; M CHAMMA; S BOTTE et al. 2009. Molecular characterization of a new spontaneous genetic rat model of generalized epilepsy with absense seizures (aes 63rd annual meeting of the american epilepsy society 2009). In: Aes 63rd annual meeting of the american epilepsy society 2009. Estados Unidos.
  76. Life Sciences Neuroscience (miscellaneous)
    Fábio Frangiotti CONTE; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Lourenço Sbragia NETO; Rovilson GILIOLI; Iscia Teresinha Lopes CENDES. 2008. Investigating the role of mrib-72-1/efhc1 in brain development by gene expression profiling (60th annual meeting of american academy of neurology). In: 60th annual meeting of american academy of neurology. Estados Unidos.
  77. Life Sciences Neuroscience (miscellaneous)
    Danyella Barbosa DOGINI; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Cristiane De Souza ROCHA; Tiago Campos PEREIRA; Iscia Teresinha Lopes CENDES. 2008. Microrna expression profile during embryonic central nervous system development (60th annual meeting of american academy of neurology). In: 60th annual meeting of american academy of neurology. Estados Unidos.
  78. Health Sciences Neurology (clinical)
    Mariana Saragiotto Da SILVA; Kellen Manoela SIQUEIRA; E BILEVICIUS; Rodrigo SECOLIN; Marilza Samtos LIMA et al. 2008. Significant association between polymorphisms in a drug-transporter gene (atp-binding cassette family - abcc2) and pharmacoresistance to antiepileptic drug therapy in mesial temporal lobe epilepsy (60th annual meeting of american academy of neurology). In: 60th annual meeting of american academy of neurology. Estados Unidos.
  79. Life Sciences Neurology
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; C L YASUDA; Luciana Cardoso BONADIA; Marilza Samtos LIMA et al. 2008. Voxel-based morphometry shows deep white matter damage in friedreich ataxia (60th annual meeting of american academy of neurology). In: 60th annual meeting of american academy of neurology. Estados Unidos.
  80. Health Sciences Neurology (clinical)
    Alberto Luiz Cunha Da COSTA; Carlos Alberto Mantovani GUERREIRO; Iscia Teresinha Lopes CENDES; Vera Lúcia G S LOPES. 2008. Frequency of major congenital malformations and dysmorphic signs in the offspring of women with epilepsy followed prospectively during pregnancy. In: 60th annual meeting of american academy of neurology. Estados Unidos.
  81. Health Sciences Neurology (clinical)
    Cláudia V Maurer MORELLI; Romenia Ramos DOMINGUES; Helder TEDESCHI; Evandro P L De OLIVEIRA; Fernando CENDES et al. 2008. Expression of ptprm gene is increased in surgical speciments of patients with medically refractory mesial temporal lobe epilepsy with hippocampal atrophy (60th annual meeting of american academy of neurology). In: 60th annual meeting of american academy of neurology. Estados Unidos.
  82. Health Sciences Neurology (clinical)
    Alberto Luiz Cunha Da COSTA; Iscia Teresinha Lopes CENDES; Carlos Alberto Mantovani GUERREIRO. 2008. Seizure frequency during pregnancy in two consecutive cohorts of women with epilepsy (60th annual meeting of the american academy of neurology). In: 60th annual meeting of the american academy of neurology. Estados Unidos.
  83. Life Sciences Cellular and Molecular Neuroscience
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; C L YASUDA; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2008. Gray and white matter atrophy revealed by voxel-based morphometry (vbm) in machado-joseph disease (60th annual meeting of the american academy of neurology). In: 60th annual meeting of the american academy of neurology. Estados Unidos.
  84. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Eliane KOBAYASHI; M E MORITA; C L YASUDA; Iscia Teresinha Lopes CENDES et al. 2008. Volumetric and mri voxel-based-morphometry analysis in patients with benign temporal lobe epilepsy (60th annual meeting of the american academy of neurology). In: 60th annual meeting of the american academy of neurology. Estados Unidos.
  85. Life Sciences Neurology
    Luís E G G BETTING; M E MORITA; C L YASUDA; Iscia Teresinha Lopes CENDES; Marilisa Mantovani GUERREIRO et al. 2008. Investigation of neuroanatomical abnormalities of the generalized tonic-clonic seizures (60th annual meeting of the american academy of neurology). In: 60th annual meeting of the american academy of neurology. Estados Unidos.
  86. Life Sciences Neurology
    Tiago Campos PEREIRA; Vinicius D Ávila Bittencourt PASCOAL; Iscia Teresinha Lopes CENDES. 2008. Human herpesvirus 6b does not decrease eaat2 transcript levels through rna interference (rnai) mediated gene silencing (60th annual meeting of the american academy of neurology). In: 60th annual meeting of the american academy of neurology. Estados Unidos.
  87. Life Sciences Neuroscience (miscellaneous)
    Vinicius D Ávila Bittencourt PASCOAL; Rafael B MARCHESINI; Esper Abrão CAVALHEIRO; Iscia Teresinha Lopes CENDES. 2008. Estudo funcional de genes inflamatórios da fase aguda em modelo animal de epilepsia do lobo temporal (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  88. Life Sciences Neuroscience (miscellaneous)
    Rodrigo SECOLIN; Cristiane De Souza ROCHA; Cláudia V Maurer MORELLI; M E MORITA; Fernando CENDES et al. 2008. Mapeando genes que influenciam a gravidade da doença na epilepsia de lobo temporal mesial familiar (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  89. Health Sciences Neurology (clinical)
    Cláudia V Maurer MORELLI; Romenia Ramos DOMINGUES; Cristiane De Souza ROCHA; Rodrigo SECOLIN; Helder TEDESCHI et al. 2008. Estudos moleculares na epilepsia de lobo temporal mesial associada à atrofia hipocampal (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  90. Life Sciences Neurology
    Luís E G G BETTING; M E MORITA; C L YASUDA; Iscia Teresinha Lopes CENDES; Marilisa Mantovani GUERREIRO et al. 2008. Investigação quantitativa multimodal das focalidades presentes no eeg de pacientes com epilepsia generalizada idiopática (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  91. Health Sciences Neurology (clinical)
    L CONZ; M E MORITA; Ana Carolina COAN; C L YASUDA; A R PEREIRA et al. 2008. Análise longitudinal da atrofia de estruturas mesiais do lobo temporal em pacientes com epilepsia de lobo temporal mesial familiar (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  92. Life Sciences Neuroscience (miscellaneous)
    M E MORITA; L CONZ; Cláudia V Maurer MORELLI; Eliane KOBAYASHI; C L YASUDA et al. 2008. Avaliação prospectiva de pacientes com epilepsia de lobo temporal mesial familiar (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  93. Health Sciences Neurology (clinical)
    Vinicius D Ávila Bittencourt PASCOAL; Tiago Campos PEREIRA; Ivan Godoy MAIA; Iscia Teresinha Lopes CENDES. 2008. Human herpervirus 6b does not directly interfere with eaat2 gene through rnai related events (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  94. Health Sciences Neurology (clinical)
    Mariana Saragiotto Da SILVA; Kellen Manoela SIQUEIRA; E BILEVICIUS; Rodrigo SECOLIN; Marilza Santos SILVA et al. 2008. Snp analysis in a drug-transporter gene (atp-binding cassette family - abcc2) suggest an association with pharmacoresistence in patients with mesial temporal lobe epilepsy (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  95. Life Sciences Neuroscience (miscellaneous)
    Danyella Barbosa DOGINI; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Cristiane De Souza ROCHA; Tiago Campos PEREIRA; Helder TEDESCHI et al. 2008. Quantification of microrna in central nervous system development and cortical dysplasia (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  96. Life Sciences Neuroscience (miscellaneous)
    Kellen Manoela SIQUEIRA; Iscia Teresinha Lopes CENDES; Fernando CENDES; M S SILVA; Rodrigo SECOLIN et al. 2008. The influence of polymorphisms in the abcb1 (mdr1) gene in the response to anti-epileptic drugs in mesial temporal lobe epilepsy. In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  97. Health Sciences Medicine (miscellaneous)
    Simone Sayuri TSUNEDA; Daniela Aguiar De Souza KOLS; Fábio Rossi TORRES; Rodrigo SECOLIN; Cláudia V Maurer MORELLI et al. 2008. Estudo genético de famílias com polimicrogiria perisylviana bilateral congênita: screening de mutações no gene srpx2 (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  98. Life Sciences Neurology
    Marcelo Jun MURAI; L C ALMEIDA; André Henrique ZAMBONI; R HORIUCHI; D MARTINS et al. 2008. Proteomic analysis in mesial temporal lobe epilepsy (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  99. Life Sciences Neurology
    Daniela Aguiar De Souza KOLS; Fábio Rossi TORRES; Simone Sayuri TSUNEDA; Iara Leda Brandão De ALMEIDA; Marilisa Mantovani GUERREIRO et al. 2008. Mutations in the emx2 gene are not present in patients with schizencephaly and polymicrogyria (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  100. Life Sciences Neurology
    Rafael B MARCHESINI; Vinicius D Ávila Bittencourt PASCOAL; Esper Abrão CAVALHEIRO; Iscia Teresinha Lopes CENDES. 2008. Gene functional studies in the silent phase of the pilocarpine model (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  101. Life Sciences Neurology
    Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Lourenço Sbragia NETO; Rovilson GILIOLI; Francesco LANGONI; Fábio Frangiotti CONTE et al. 2008. Lgi1 gene studies in mouse central nervous system (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  102. Health Sciences Neurology (clinical)
    M C GONSALES; L C FONSECA; G M A S TEDRUS; Iscia Teresinha Lopes CENDES. 2008. Triagem de mutações em genes candidatos para a epilepsia benigna da infância com espículas centro-temporais (xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica). In: Xxxii congresso brasileiro de epilepsia / xviii jornada brasileira de neurofisiologia clínica. Brasil.
  103. Health Sciences Neurology (clinical)
    Susana Barreto MORY; Luís E G G BETTING; Iscia Teresinha Lopes CENDES; Marilisa Mantovani GUERREIRO; Carlos Alberto Mantovani GUERREIRO et al. 2008. Envolvimento do tálamo na patogênese da epilepsia mioclônica juvenil (xxiii congresso brasileiro de neurologia; viii encontro luso-brasileiro de neurologia; i encontro pan-amazônico de neurologia tropical e viii encontro da sociedade brasileira de investigação neurológica- sbin). In: Xxiii congresso brasileiro de neurologia; viii encontro luso-brasileiro de neurologia; i encontro pan-amazônico de neurologia tropical e viii encontro da sociedade brasileira de investigação neurológica- sbin. Brasil.
  104. Life Sciences Neurology
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; C L YASUDA; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2008. Correlação entre sintomas motores e grau de atrofia cerebelar em pacientes com doença de machado-joseph (xxiii congresso brasileiro de neurologia; viii encontro luso-brasileiro de neurologia; i encontro pan-amazônico de neurologia tropical e viii encontro da sociedade brasileira de investigação neurológica- sbin). In: Xxiii congresso brasileiro de neurologia; viii encontro luso-brasileiro de neurologia; i encontro pan-amazônico de neurologia tropical e viii encontro da sociedade brasileira de investigação neurológica- sbin. Brasil.
  105. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Talita M MARIN; C F CLEMENTE; Aline M SANTOS; Paty K PICARDI; Vinicius D Ávila Bittencourt PASCOAL et al. 2008. Shp 2 negatively regulates growth in cardiac myocytes by controling focal adhesion kinase and mtor/s6 kinase pathways (xxiii reunião anual da federação de sociedades de biologia experimental - fesbe). In: Xxiii reunião anual da federação de sociedades de biologia experimental - fesbe. Brasil.
  106. Life Sciences Neuroscience (miscellaneous)
    Vinicius D Ávila Bittencourt PASCOAL; Marchesini Rafael BREGLIO; Tiago Campos PEREIRA; Rovilson GILIOLI; Esper Abrão CAVALHEIRO et al. 2008. Uso da interferência por rna (rnai) no estudo funcional de genes inflamatórios da fase aguda no modelo animal de epilepsia do lobo temporal induzido pela pilocarpina (xxiii reunião anual da federação de sociedades de biologia experimental - fesbe). In: Xxiii reunião anual da federação de sociedades de biologia experimental - fesbe. Brasil.
  107. Physical Sciences Chemistry (miscellaneous)
    Sassonia R; Marcelo Jun MURAI; M G De OLIVEIRA; Iscia Teresinha Lopes CENDES. 2008. Isothermal titration calorimetry on bindign to human (4º simpósio brasileiro em química medicinal). In: 4º simpósio brasileiro em química medicinal. Brasil.
  108. Health Sciences Neurology (clinical)
    Fábio Rossi TORRES; Daniela Aguiar De Souza KOLS; Simone Sayuri TSUNEDA; Rodrigo SECOLIN; Iara Leda Brandão De Almeida PEREIRA et al. 2008. Estudos genéticos e moleculares em um grande grupo de pacientes com malformações do córtex cerebral (xxxii congresso brasileiro de epilepsia). In: Xxxii congresso brasileiro de epilepsia. Brasil.
  109. Health Sciences Neurology (clinical)
    M E MORITA; L CONZ; Cláudia V Maurer MORELLI; Eliane KOBAYASHI; C L YASUDA et al. 2008. Lobg term follow up of familial mesial temporal lobe epilepsy (xxxii congresso brasileiro de epilepsia). In: Xxxii congresso brasileiro de epilepsia. Brasil.
  110. Life Sciences Neurology
    Luís E G G BETTING; Li Li MIN; Iscia Teresinha Lopes CENDES; Marilisa Mantovani GUERREIRO; Carlos Alberto Mantovani GUERREIRO et al. 2008. Pacientes com epilepsia generalizada idiopática apresentam focalidades estruturais e funcionais (xxiii congresso brasileiro de neurologia; viii encontro luso-brasileiro de neurologia; i encontro pan-amazônico de neurologia tropical e viii encontro da sociedade brasileira de investigação neurológica- sbin). In: Xxiii congresso brasileiro de neurologia; viii encontro luso-brasileiro de neurologia; i encontro pan-amazônico de neurologia tropical e viii encontro da sociedade brasileira de investigação neurológica- sbin. Brasil.
  111. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 2007. Síndromes epilépticas geneticamente determinadas: aspectos clínicos e moleculares (1st latin american summer school on epilepsy). In: 1st latin american summer school on epilepsy. Brasil.
  112. Health Sciences Medicine (miscellaneous)
    A WOLF; L MOURDO; H BEIKE; M FRANG; A SILVA et al. 2007. Swallowing in machado-joseph´s disease: preliminary study of 7 cases (the fifteenth annual dysphagia research society meeting). In: The fifteenth annual dysphagia research society meeting. Canadá.
  113. Life Sciences Neurology
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Luciana Cardoso BONADIA; Marilza Santos SILVA; Iscia Teresinha Lopes CENDES et al. 2007. Cerebral white matter dysfunction in friedreich´s ataxia: a 1h-mrs study (59th american academy of neurology annual meeting). In: 59th american academy of neurology annual meeting. Estados Unidos.
  114. Health Sciences Neurology (clinical)
    Cláudia Viana Maurer MORELLI; Rodrigo SECOLIN; Romenia Ramos DOMINGUES; Rafael B MARCHESINI; Neide F SANTOS et al. 2007. Identification of the locus for familial mesial temporal lobe epilepsy with hippocampal atrophy and search for candidate genes (59th american academy of neurology annual meeting). In: 59th american academy of neurology annual meeting. Estados Unidos.
  115. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2007. Protein structural studies in poliq disorders (xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb)). In: Xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb). Brasil.
  116. Life Sciences Developmental Biology
    Danyella Barbosa DOGINI; Iscia Teresinha Lopes CENDES. 2007. Microrna expression pattern during embryonic central nervous system development (xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb)). In: Xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb). Brasil.
  117. Health Sciences Medicine (miscellaneous)
    Mariana Saragiotto Da SILVA; Iscia Teresinha Lopes CENDES. 2007. Are polymorphisms in candidate gene associated with drug metabolism and ion channels and pharmacoresistance in epilepsy? (xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb)). In: Xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb). Brasil.
  118. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Vnícius D Avila Bittencourt PASCOAL; Iscia Teresinha Lopes CENDES. 2007. Computational identification of best rnai targets based on free energy features (xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb)). In: Xxxvi annual meeting of the brazilian society for biochemistry and molecular biology - sbbq and 10th international union of biochemistry and molecular biology (iubmb). Brasil.
  119. Life Sciences Neuroscience (miscellaneous)
    Heloisa Helena RUOCCO; Iscia Teresinha Lopes CENDES; Li Li MIN; F CENDES. 2007. Evidence of thalamic dysfunction in huntington disease by proton magnetic resonance spectroscopy (vi congresso paulista de neurologia). In: Vi congresso paulista de neurologia. Brasil.
  120. Life Sciences Neuroscience (miscellaneous)
    Heloisa Helena RUOCCO; Leonardo BONILHA; Li Li MIN; Iscia Teresinha Lopes CENDES; F CENDES. 2007. Longitudinal analysis of regional gray matter loss in huntington´s disease: effects of the length of the cag repeat. (vi congresso paulista de neurologia). In: Vi congresso paulista de neurologia. Brasil.
  121. Life Sciences Neuroscience (miscellaneous)
    Fábio Rossi TORRES; E BILEVICIUS; R SECOLIN; N F SANTOS; Eliane KOBAYASHI et al. 2007. Estudo de ligação em uma família com epilepsia do lobo temporal com sintomas auditivos (eltsa) identifica um novo lócus candidato em 1p36 (53º congresso brasileiro de genética). In: 53º congresso brasileiro de genética. Brasil.
  122. Life Sciences Genetics
    Rodrigo SECOLIN; Cristiane De Souza ROCHA; Iscia Teresinha Lopes CENDES. 2007. Validação de nova estratégia estatística para mapeamento de genes modificadores em síndromes complexas (53º congresso brasileiro de genética). In: 53º congresso brasileiro de genética. Brasil.
  123. Life Sciences Animal Science and Zoology
    C M LOPES; Vinicius D Ávila Bittencourt PASCOAL; Rafael B MARCHESINI; Iscia Teresinha Lopes CENDES. 2007. Seleção de seqüências-alvo ideais para confecção de sirna direcionadas ao gene interleucina 1b em ratos wistars (53º congresso brasileiro de genética). In: 53º congresso brasileiro de genética. Brasil.
  124. Life Sciences Genetics
    Mariana Saragiotto Da SILVA; K M SIQUEIRA; N C IANNI; E BILEVICIUS; M L SANTOS et al. 2007. Polimorfismos em genes candidatos estão associados à farmacoresistência em epilepsia? (53º congresso brasileiro de genética). In: 53º congresso brasileiro de genética. Brasil.
  125. Health Sciences Neurology (clinical)
    André Henrique ZAMBONI; Iscia Teresinha Lopes CENDES. 2007. Análise estrutural da proteína efhc1; relacionada à epilepsia mioclônica juvenil (xv congresso interno de iniciação científica da unicamp). In: Xv congresso interno de iniciação científica da unicamp. Brasil.
  126. Life Sciences Neuroscience (miscellaneous)
    L CONZ; M E MORITA; Ana Carolina COAN; Eliane KOBAYASHI; C L YASUDA et al. 2007. Análise longitudinal da atrofia de estruturas mesiais do lobo temporal em pacientes com epilepsia de lobo temporal mesial familiar (xxi congresso brasileiro de neurofisiologia clínica / xxxi reunião da liga brasileira de epilepsia). In: Xxi congresso brasileiro de neurofisiologia clínica / xxxi reunião da liga brasileira de epilepsia. Brasil.
  127. Life Sciences Neuroscience (miscellaneous)
    Luís E G G BETTING; M E MORITA; C L YASUDA; Carlos Alberto Mantovani GUERREIRO; Marilisa Mantovani GUERREIRO et al. 2007. Avaliação estrutural em pacientes com crises tônico-clônicas generalizadas através da morfometria baseada em voxel (xxi congresso brasileiro de neurofisiologia clínica / xxxi reunião da liga brasileira de epilepsia). In: Xxi congresso brasileiro de neurofisiologia clínica / xxxi reunião da liga brasileira de epilepsia. Brasil.
  128. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Camila Miranda LOPES; Iscia Teresinha Lopes CENDES. 2007. Desenhos de moléculas de sirna contra o gene bdnf em ratos wistars (xv congresso interno de iniciação científica da unicamp). In: Xv congresso interno de iniciação científica da unicamp. Brasil.
  129. Life Sciences Neuroscience (miscellaneous)
    Daniela Aguiar De SOUZA; Iscia Teresinha Lopes CENDES. 2007. Investigação das bases moleculares dos distúrbios do desenvolvimento cortical (ddc) - (xv congresso interno de iniciação científica da unicamp). In: Xv congresso interno de iniciação científica da unicamp. Brasil.
  130. Health Sciences Medicine (miscellaneous)
    Karla De Abreu BARBOSA; Iscia Teresinha Lopes CENDES. 2007. O papel das mutações no gene efhc1 na etiologia da epilepsia mioclônica juvenil (xv congresso interno de iniciação científica da unicamp). In: Xv congresso interno de iniciação científica da unicamp. Brasil.
  131. Health Sciences Medicine (miscellaneous)
    Kellen Manoela SIQUEIRA; Iscia Teresinha Lopes CENDES. 2007. Avaliação farmacogenética da resposta ao tratamento medicamentoso em pacientes com epilepsia de lobo temporal mesial (xv congresso interno de iniciação científica da unicamp). In: Xv congresso interno de iniciação científica da unicamp. Brasil.
  132. Life Sciences Genetics
    Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Iscia Teresinha Lopes CENDES. 2007. Padrão de expressão do gene lgi1 em cérebros de roedores (1ª semana da pesquisa da fcm). In: 1ª semana da pesquisa da fcm. Brasil.
  133. Life Sciences Neuroscience (miscellaneous)
    Mariana Saragiotto Da SILVA; Iscia Teresinha Lopes CENDES. 2007. Investigação da relação entre polimorfismos genéticos e refratariedade medicamentosa na epilepsia de lobo temporal (1ª semana da pesquisa da fcm). In: 1ª semana da pesquisa da fcm. Brasil.
  134. Life Sciences Genetics
    Daniela Aguiar De SOUZA; Iscia Teresinha Lopes CENDES. 2007. Triagem de mutações em um grupo de pacientes com distúrbios do desenvolvimento cortical (1ª semana da pesquisa da fcm). In: 1ª semana da pesquisa da fcm. Brasil.
  135. Life Sciences Neuroscience (miscellaneous)
    Fábio Frangiotti CONTE; Iscia Teresinha Lopes CENDES. 2007. Análise da expressão do gene mrib72-1/efhc1 durante o desenvolvimento do sistema nervoso central (1ª semana da pesquisa da fcm). In: 1ª semana da pesquisa da fcm. Brasil.
  136. Life Sciences Neuroscience (miscellaneous)
    Camila Fernanda LOPES; Iscia Teresinha Lopes CENDES. 2007. Padronização do modelo de epilepsia induzida pela pilocarpina em animais provenientes do cemib e desenho de moléculas de sirna. In: 1ª semana da pesquisa da fcm. Brasil.
  137. Life Sciences Neuroscience (miscellaneous)
    Danyella Barbosa DOGINI; Iscia Teresinha Lopes CENDES. 2007. Expressão de micrornas durante o desenvolvimento do sistema nervoso central (1ª semana da pesquisa da fcm). In: 1ª semana da pesquisa da fcm. Brasil.
  138. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Danyella Barbosa DOGINI; Patricia Aline Oliveira RIBEIRO; Tiago Campos PEREIRA; Cristiane De Souza ROCHA; Iscia Teresinha Lopes CENDES. 2007. Quantification of microrna during centrla nervous system development (57 annual meeting of the american society of human genetics). In: 57 annual meeting of the american society of human genetics. Estados Unidos.
  139. Health Sciences Medicine (miscellaneous)
    Mariana Saragiotto Da SILVA; Kellen Manoela SIQUEIRA; N C IANNI; E BILEVICIUS; Fernando CENDES et al. 2007. Impact of polymorphisms in candidate genes for pharmacoresistance in mesial temporal lobe epilepsy (57 annual meeting of the american society of human genetics). In: 57 annual meeting of the american society of human genetics. Estados Unidos.
  140. Life Sciences Genetics
    Rodrigo SECOLIN; Cristiane De Souza ROCHA; Iscia Teresinha Lopes CENDES. 2007. A new statistical approach for mapping modifier genes taken advantage of family structure (57 annual meeting of the american society of human genetics). In: 57 annual meeting of the american society of human genetics. Estados Unidos.
  141. Life Sciences Genetics
    Fábio Rossi TORRES; E BILEVICIUS; Rodrigo SECOLIN; Neide F SANTOS; Eliane KOBAYASHI et al. 2007. Mapping a new candidate locus for autosomal dominant partial epilepsy with auditory features (57 annual meeting of the american society of human genetics). In: 57 annual meeting of the american society of human genetics. Estados Unidos.
  142. Health Sciences Neurology (clinical)
    Cláudia V Maurer MORELLI; Cristiane De Souza ROCHA; Rodrigo SECOLIN; Romenia Ramos DOMINGUES; Fernando CENDES et al. 2007. Analysis of gene expression in familial mesial temporal lobe epilepsy associated with hippocampal atrophy (57 annual meeting of the american society of human genetics). In: 57 annual meeting of the american society of human genetics. Estados Unidos.
  143. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; Anderson TAVARES; Iscia Teresinha Lopes CENDES; Cláudia V Maurer MORELLI; Rodrigo SECOLIN et al. 2007. Analysis of candidate loci in primary open angle glaucoma families (57 annual meeting of the american society of human genetics). In: 57 annual meeting of the american society of human genetics. Estados Unidos.
  144. Health Sciences Genetics (clinical)
    Cristiane De Souza ROCHA; Iscia Teresinha Lopes CENDES. 2007. Affymetrix annotation search; a tool for data mining with affymetrix data (57 annual meeting of the american society of human genetics). In: 57 annual meeting of the american society of human genetics. Estados Unidos.
  145. Life Sciences Neuroscience (miscellaneous)
    Erika Lopes Burrone De FREITAS; Silvyo David Araújo GIFFONI; Milena SIMIONI; Iscia Teresinha Lopes CENDES; Vera Lúcia G S LOPES. 2006. Determinação de estratégia de investigação molecular de defeitos de linha média facial com hipertelorismo baseada em correlação dismorfológica e neurológica. In: Xviii congresso brasileiro de genética clínica. Brasil.
  146. Life Sciences Genetics
    Maria Fernanda Ribeiro BITTAR; Iscia Teresinha Lopes CENDES. 2006. O consentimento livre e esclarecido para o sujeito de pesquisa: uma análise qualitativa (xviii congresso brasileiro de genética clínica). In: Xviii congresso brasileiro de genética clínica. Brasil.
  147. Life Sciences Genetics
    Danilo Vilela VIANA; Juvenal Ricardo Navarro GOES; Cláudio Saddy Rodrigues COY; Maria De Lourdes Setsuko AYRIZONO; Carmen Silvia Passos LIMA et al. 2006. História familial de câncer nos pacientes com diagnóstico de câncer de cólon e reto no hospital de clínicas da unicamp (xviii congresso brasileiro de genética clínica). In: Xviii congresso brasileiro de genética clínica. Brasil.
  148. Health Sciences Medicine (miscellaneous)
    Marjory Alana MARCELLO; Cláudia V Maurer MORELLI; Iscia Teresinha Lopes CENDES. 2006. Estudo de ligação com o emprego de marcadores microssatélites na busca do locus para a epilepsia do lobo temporal mesial familial. In: Xiv congresso interno de iniciação científica da unicamp 2006. Brasil.
  149. Physical Sciences Biomedical Engineering
    Romenia Ramos DOMINGUES; Cláudia V Maurer MORELLI; Iscia Teresinha Lopes CENDES. 2006. Triagem de mutações pelo método da desnaturação em cromatografia líquida de alta performance (dhplc). In: Xiv congresso interno de iniciação científica da unicamp 2006. Brasil.
  150. Life Sciences Neuroscience (miscellaneous)
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO et al. 2006. Análise molecular de pacientes com distúrbios do desenvolvimento cortical (ddc) - (xiv congresso interno de iniciação científica da unicamp). In: Xiv congresso interno de iniciação científica da unicamp 2006. Brasil.
  151. Life Sciences Neuroscience (miscellaneous)
    André Henrique ZAMBONI; Marcelo Jun MURAI; Fábio F CONTE; Iscia Teresinha Lopes CENDES. 2006. Análise estrutural e funcional de proteínas relacionadas à epileptogênese humana (xiv congresso interno de iniciação científica da unicamp). In: Xiv congresso interno de iniciação científica da unicamp 2006. Brasil.
  152. Health Sciences Genetics (clinical)
    Rodrigo SECOLIN; Neide F SANTOS; Iara Leda Brandão De ALMEIDA; Marilza Santos SILVA; Marilisa Mantovani GUERREIRO et al. 2006. Identificação de um novo locus para polimicrogiria perisylviana bilateral congênita (ppbc) no cromossomo xq27 - q28 (xiv congresso interno de iniciação científica da unicamp). In: Xiv congresso interno de iniciação científica da unicamp 2006. Brasil.
  153. Life Sciences Neurology
    R V AZEVEDO; Marcondes Cavalcante França JUNIOR; A V FARIA; F R PEREIRA; Iscia Teresinha Lopes CENDES et al. 2006. A family with horizontal gaze palsy and progressive scoliosis (hgpps) - (xxii congresso brasileiro de neurologia; vi encontro luso-brasileiro de neurologia e ii congresso da federação latino-americana de neurologia - neurosur). In: Xxii congresso brasileiro de neurologia; vi encontro luso-brasileiro de neurologia e ii congresso da federação latino-americana de neurologia - neurosur. Brasil.
  154. Life Sciences Neurology
    Heloisa Helena RUOCCO; Leonardo BONILHA; P A RIO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2006. Análise longitudinal das anormalidades da distribuição regional da substância cinzenta na doença de huntington (xxii congresso brasileiro de neurologia; vi encontro luso-brasileiro de neurologia e ii congresso da federação latino-americana de neurologia - neurosur). In: Xxii congresso brasileiro de neurologia; vi encontro luso-brasileiro de neurologia e ii congresso da federação latino-americana de neurologia - neurosur. Brasil.
  155. Life Sciences Genetics
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO et al. 2006. Desordens do desenvolvimento cortical: estudo molecular de um grupo de pacientes (52º congresso brasileiro de genética). In: 52º congresso brasileiro de genética. Brasil.
  156. Life Sciences Genetics
    Rodrigo SECOLIN; Neide F SANTOS; Marilza S SILVA; Iara Leda Brandão De ALMEIDA; Fernando CENDES et al. 2006. Inativação preferencial do cromossomo x em famílias com polimicrogiria perysilviana bilateral congênita (52º congresso brasileiro de genética). In: 52º congresso brasileiro de genética. Brasil.
  157. Life Sciences Genetics
    Fabio Rossi TORRES; Neide F SANTOS; Rodrigo SECOLIN; M C GONÇALVES; Eliane KOBAYASHI et al. 2006. Estudo de ligação em uma família com epilepsia do lobo temporal autossômica dominante (eltad) sem mutações no gene lgi1 (52º congresso brasileiro de genética). In: 52º congresso brasileiro de genética. Brasil.
  158. Life Sciences Genetics
    Simone Sayuri TSUNEDA; Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES et al. 2006. Estudo molecular de mecanismo de mutação no gene fln1 em pacientes portadores de heterotopia nodular periventricular bilateral (hnpb) - (52º congresso brasileiro de genética). In: 52º congresso brasileiro de genética. Brasil.
  159. Health Sciences Medicine (miscellaneous)
    Marcelo Jun MURAI; R HORIUCHI; D MARTINS; Cláudia V Maurer MORELLI; J C NOVELLO et al. 2006. Análise 2 de-dige de epilepsia do lobo temporal mesial (52º congresso brasileiro de genética). In: 52º congresso brasileiro de genética. Brasil.
  160. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Rodrigo SECOLIN; Cristiane ROCHA; Iscia Teresinha Lopes CENDES. 2006. Um novo algoritmo para manipulação de dados nos estudos de ligação genética em doenças humanas. In: 52º congresso brasileiro de genética. Brasil.
  161. Life Sciences Genetics
    Vinicius D Ávila Bittencourt PASCOAL; Patricia Aline Oliveira RIBEIRO; Luís E G G BETTING; Neide F SANTOS; Carlos Alberto Mantovani GUERREIRO et al. 2006. Identificação de mutações no gene efhc1 em pacientes com epilepsia mioclônica juvenil (emj) - (52º congresso brasileiro de genética). In: 52º congresso brasileiro de genética. Brasil.
  162. Health Sciences Neurology (clinical)
    A L COSTA; Carlos Alberto Mantovani GUERREIRO; Maria Augusta S MONTENEGRO; Iscia Teresinha Lopes CENDES; Vera L G S LOPES. 2006. Malformações e alterações de desenvolvimento em filhos de mães com epilepsia (4º congreso latinoamericano de epilepsia guatemala). In: 4º congreso latinoamericano de epilepsia guatemala 2006. Guatemala.
  163. Life Sciences Neuroscience (miscellaneous)
    Patricia Aline Oliveira RIBEIRO; Lourenço SBRAGIA; Rovilson GIGLIOLI; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Padrão de expressão do gene lgi1 em sistema nervoso central de roedores sugere possível função (4º congreso latinoamericano de epilepsia guatemal). In: 4º congreso latinoamericano de epilepsia guatemala 2006. Guatemala.
  164. Life Sciences Neuroscience (miscellaneous)
    Fábio Frangiotti CONTE; Rovilson GIGLIOLI; Lourenço SBRAGIA; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Estudo da expresão do gene mrib72-1/efhc1 durante o desenvolvimento do sistema nervoso central (4º congreso latinoamericano de epilepsia guatemala). In: 4º congreso latinoamericano de epilepsia guatemala 2006. Guatemala.
  165. Life Sciences Neurology
    Simone Sayuri TSUNEDA; Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES et al. 2006. Análise molecular de mutação no gene fln1 em pacientes portadores de heterotopia nodular periventricular bilateral (hnpb) - (4º congreso latinoamericano de epilepsia guatemala). In: 4º congreso latinoamericano de epilepsia guatemala 2006. Guatemala.
  166. Health Sciences Neurology (clinical)
    Fábio Rossi TORRES; Rodrigo SECOLIN; Neide F SANTOS; Marina Coelho GONSALVES; Eliane KOBAYASHI et al. 2006. Searching for the second locus for autosomal dominant lateral temporal lobe epilepsy (adltle) - (4º congreso latinoamericano de epilepsia guatemala). In: 4º congreso latinoamericano de epilepsia guatemala 2006. Guatemala.
  167. Life Sciences Neurology
    Vinicius D Ávila Bittencourt PASCOAL; Patricia Aline Oliveira RIBEIRO; Luís E G G BETTING; Neide F SANTOS; Susana Barreto MORY et al. 2006. Frequência de mutações no gene efhc1 em pacientes brasileiros com epilepsia mioclônica juvenil (emj) - (4º congreso latinoamericano de epilepsia guatemala). In: 4º congreso latinoamericano de epilepsia guatemala 2006. Guatemala.
  168. Health Sciences Neurology (clinical)
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; M RODRIGUES; Maria Augusta S MONTENEGRO et al. 2006. Mutation screening in candidate genes in a large cohort of patients with cortical malformations (4º congreso latinoamericano de epilepsia guatemala). In: 4º congreso latinoamericano de epilepsia guatemala 2006. Guatemala.
  169. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Fábio Frangiotti CONTE; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Lourenço Sbragia NETO; Rovilson GILIOLI; Fernando CENDES et al. 2006. Analysis of the expression of mrib72-1/efhc 1 gene during mouse brain development (56th annual meeting of the american society of human genetics). In: 56th annual meeting of the american society of human genetics. Estados Unidos.
  170. Life Sciences Developmental Biology
    Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Lourenço Sbragia NETO; Rovilson GILIOLI; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Expression pattern of lgi1 in mouse brain during development suggests a possible function (56th annual meeting of the american society of human genetics). In: 56th annual meeting of the american society of human genetics. Estados Unidos.
  171. Life Sciences Genetics
    Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Molecular analysis of a novel fln1 gene mutation (56th annual meeting of the american society of human genetics). In: 56th annual meeting of the american society of human genetics. Estados Unidos.
  172. Life Sciences Neuroscience (miscellaneous)
    Marcelo Jun MURAI; R HORIUCHI; D MARTINS; Cláudia Viana Maurer MORELLI; J C NOVELLO et al. 2006. 2de-dige proteomic analysis in mesial temporal lobe epilepsy. In: 56th annual meeting of the american society of human genetics. Estados Unidos.
  173. Life Sciences Neurology
    Fábio Rossi TORRES; Neide F SANTOS; Rodrigo SECOLIN; M C GONSALES; Eliane KOBAYASHI et al. 2006. Linkage studies in autosomal dominant lateral temporal lobe epilepsy: searching for the alternative locus (56th annual meeting of the american society of human genetics). In: 56th annual meeting of the american society of human genetics. Estados Unidos.
  174. Health Sciences Medicine (miscellaneous)
    Cláudia Viana Maurer MORELLI; Rodrigo SECOLIN; Romenia Ramos DOMINGUES; Rafael B MARCHESINI; Neide F SANTOS et al. 2006. A locus for familial mesial temporal lobe epilepsy mapped on chromosome 18p (56th annual meeting of the american society of human genetics). In: 56th annual meeting of the american society of human genetics. Estados Unidos.
  175. Life Sciences Neuroscience (miscellaneous)
    Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Lourenço Sbragia NETO; Rovilson GILIOLI; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Insigts into lgi1 gene function in mouse brain (1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy). In: 1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy. Estados Unidos.
  176. Life Sciences Neuroscience (miscellaneous)
    Marcelo Jun MURAI; R HORIUCHI; D MARTINS; Cláudia Viana Maurer MORELLI; Jose Camillo NOVELLO et al. 2006. 2de-dige proteomic analysis in mesial temporal lobe epilepsy. In: 1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy. Estados Unidos.
  177. Health Sciences Neurology (clinical)
    Cláudia Viana Maurer MORELLI; Rodrigo SECOLIN; Romenia Ramos DOMINGUES; Rafael B MARCHESINI; Neide F SANTOS et al. 2006. Genome-wide linkage study identifies a locus for familial mesial temporal lobe epilepsy (1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy). In: 1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy. Estados Unidos.
  178. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Simone Sayuri TSUNEDA; Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES et al. 2006. Molecular analysis of a novel fln1 gene mutation found in familial bilateral periventricular nodular heterotopia. In: 1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy. Estados Unidos.
  179. Health Sciences Neurology (clinical)
    Fábio Frangiotti CONTE; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Lourenço Sbragia NETO; Rovilson GILIOLI; Fernando CENDES et al. 2006. Expression studies of mrib72-1/efhc1 gene during mouse brain development (1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy). In: 1st north american regional epilepsy congress - annual meetings of the american epilepsy society and canadian league against epilepsy. Estados Unidos.
  180. Life Sciences Neurology
    Fábio Rossi TORRES; Rodrigo SECOLIN; Neide F SANTOS; Eliane KOBAYASHI; L A C SARDINHA et al. 2005. Searching for the second locus for autosomal dominant lateral temporal lobe epilepsy. In: 57th annual meeting of the american academy of neurology. Estados Unidos.
  181. Health Sciences Medicine (miscellaneous)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2005. Mri in idiopathic generalized epilepsy: is it necessary?. In: 57th annual meeting of the american academy of neurology. Estados Unidos.
  182. Health Sciences Neurology (clinical)
    Iara Leda Brandão De ALMEIDA; Marilisa Mantovani GUERREIRO; Simone R V HAGE; Catarina GUIMARAES; Maria Augusta S MONTENEGRO et al. 2005. Congenital bilateral perisylvian syndrome (cbps): familial recurrence; clinical and psycholinguistic aspects correlated with mri. In: 55th annual meeting of the american society of human genetics. Estados Unidos.
  183. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Mariângela GRIPPO; Tiago Campos PEREIRA; Vinícius D Avila Bittencourt PASCHOAL; Patrícia Aline Oliveira RIBEIRO; Marilza Santos SILVA et al. 2005. 5'triphosphate of in vitro transcribed sirnas induce antiviral response in cell culture. In: 55th annual meeting of the american society of human genetics. Estados Unidos.
  184. Life Sciences Molecular Biology
    Maria Cristina Cabral GARCIA; C L P OLIVEIRA; Iris C L TORRIANI; Celso Eduardo BENEDETTI; Iscia Teresinha Lopes CENDES. 2005. Changes in molecular conformation of expanded ataxin-3: experimental evidence from small angle x-ray scatering (saxs) technique. In: 55th annual meeting of the american society of human genetics. Estados Unidos.
  185. Life Sciences Genetics
    Neide F SANTOS; Iara Leda Brandão De ALMEIDA; Rodrigo SECOLIN; Marilza Santos SILVA; Fernando CENDES et al. 2005. Linkage analysis for bilateral perisylvian polymicrogyria: a new locus mapped on xq27-q28. In: 55th annual meeting of the american society of human genetics. Estados Unidos.
  186. Health Sciences Psychiatry and Mental Health
    Maria Do Carmo Martins OLIVEIRA; R G M FERREIRA; Iscia Teresinha Lopes CENDES; Henrique KRIGER; Maria Fernanda Ribeiro BITTAR et al. 2005. Complex segregation analyses of bipolar affective disorder: evidence for a single major predisposing locus. In: 55th annual meeting of the american society of human genetics. Estados Unidos.
  187. Health Sciences Genetics (clinical)
    Celso Eduardo BENEDETTI; Maria Cristina Cabral GARCIA; Iscia Teresinha Lopes CENDES; C L P OLIVEIRA; Iris C L TORRIANI. 2005. Changes in molecular conformation of expanded ataxin-3: experimental evidence from small angle x-ray scatering (saxs) technique. In: Activity report 2004. Brasil.
  188. Life Sciences Genetics
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO et al. 2005. Triagem de mutações em genes relacionados ao desenvolvimento do cortex cerebral. In: Vii caeb - congresso aberto aos estudantes de biologia. Brasil.
  189. Life Sciences Neurology
    Karine Couto Sarmento TEIXEIRA; M A MONTENEGRO; Iara Leda Brandão De ALMEIDA; Iscia Teresinha Lopes CENDES; F CENDES et al. 2005. Características neurofisiológicas de pacientes com polimicrogiria. In: Xx congresso brasileiro de neurofisiologia clínica e xxx reunião da liga brasileira de epilepsia. Brasil.
  190. Life Sciences Neuroscience (miscellaneous)
    Daniela Aguiar De SOUZA; Fabio Rossi TORRES; Camila Fernanda LOPES; M A MONTENEGRO; M M GUERREIRO et al. 2005. Análise molecular em um grupo de pacientes com distúrbios do desenvolvimento cortical. In: 51º congresso brasileiro de genética. Brasil.
  191. Health Sciences Medicine (miscellaneous)
    Nilma Almeida De ASSIS; Rodrigo SECOLIN; Iscia Teresinha Lopes CENDES; Elizabeth Joao PAVIN; Maria Candida Ribeiro PARISI et al. 2005. Complicações do diabetes em uma amostra de pacientes brasileiros: associação entre rinopatia e nefropatia. In: Congresso anual da associação de diabetes juvenil. Brasil.
  192. Life Sciences Neuroscience (miscellaneous)
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; M A MONTENEGRO; Marilisa Mantovani GUERREIRO et al. 2005. Distúrbios do desenvolvimento cortical: triagem de mutações em grupo de pacientes. In: Xiii congresso interno de iniciação científica da unicamp. Brasil.
  193. Life Sciences Neurology
    Vinícius D Avila Bittencourt PASCHOAL; Iscia Teresinha Lopes CENDES. 2005. Frequência de mutações no gene efhc1 em pacientes com epilepsia mioclônica juvenil. In: Xiii congresso interno de iniciação científica da unicamp. Brasil.
  194. Life Sciences Genetics
    Rodrigo SECOLIN; Neide F SANTOS; Iara Leda Brandão De ALMEIDA; Catarina A GUIMARÃES; Ecila P M OLIVIEIRA et al. 2005. Identificação de um novo locus candidato para polimicrogiria perisylviana bilateral congênita no cromossomo xq27-q28. In: 51º congresso brasileiro de genética. Brasil.
  195. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; Patrícia Aline Oliveira RIBEIRO; Vinícius D Avila Bittencourt PASCHOAL; L E BETTING; Neide F SANTOS et al. 2005. Um novo locus candidato no cromossomo 6p para a epilepsia mioclônica juvenil. In: 51º congresso brasileiro de genética. Brasil.
  196. Health Sciences Genetics (clinical)
    Tiago Campos PEREIRA; Vinícius D Avila Bittencourt PASCHOAL; Ivan Godoy MAIA; Luis Augusto MAGALHÃES; Eliana M Zanotti MAGALHÃES et al. 2005. Development of an rnai-based treatment for shistosomiasis. In: Fesbe 2005 - xx reunião anual da federação da sociedade de biologia experimental. Brasil.
  197. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Mariangela GRIPPO; Tiago Campos PEREIRA; Rovilson GIGLIOLI; Iscia Teresinha Lopes CENDES. 2005. Rna interference against mhv-3 vírus. In: Fesbe 2005 - xx reunião anual da federação da sociedade de biologia experimental. Brasil.
  198. Life Sciences Physiology
    A M ROCHA; M P R MACHADO; Tiago Campos PEREIRA; T M ROMÃO; Patrícia Aline Oliveira RIBEIRO et al. 2005. Silenciamento do gene da enzima conversora da angiotensina por meio de interferência do rna reduz pressão arterial sistêmica em ratos espontaneamente hipertensos. In: Fesbe 2005 - xx reunião anual da federação da sociedade de biologia experimental. Brasil.
  199. Life Sciences Neuroscience (miscellaneous)
    Tiago Campos PEREIRA; Vinícius D Avila Bittencourt PASCHOAL; Ivan Godoy MAIA; Mariângela GRIPPO; Rovilson GIGLIOLI et al. 2005. Behavioral studies on mecp2- silenced mice by rna interference. In: Xxxiv reunião anual da sociedade brasileira de bioquímica e biologia molecular - sbbq. Brasil.
  200. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Míriam Gisele Gasparotto CONTESSOTTO; Maria Cristina Cabral GARCIA; Kalinca Patrícia Marengo SANTOS; Iscia Teresinha Lopes CENDES. 2005. Expression and molecular analysis of human ataxin-7. In: Xxxiv reunião anual da sociedade brasileira de bioquímica e biologia molecular - sbbq. Brasil.
  201. Health Sciences Genetics (clinical)
    Maria Cristina Cabral GARCIA; Celso Eduardo BENEDETTI; C L P OLIVEIRA; Iris C L TORRIANI; Iscia Teresinha Lopes CENDES. 2005. Human ataxin-3 structural analysis: preliminary data. In: Xxxiv reunião anual da sociedade brasileira de bioquímica e biologia molecular - sbbq. Brasil.
  202. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Marcelo Jun MURAI; Fábio Rossi TORRES; Iscia Teresinha Lopes CENDES. 2005. Human lgi1 protein expression and purification for structural and functional analyses. In: Xxxiv reunião anual da sociedade brasileira de bioquímica e biologia molecular - sbbq. Brasil.
  203. Life Sciences Molecular Biology
    Mariângela GRIPPO; Tiago Campos PEREIRA; Rovilson GIGLIOLI; Iscia Teresinha Lopes CENDES. 2005. In vitro rna interference against mhv-3 vírus. In: Xxxiv reunião anual da sociedade brasileira de bioquímica e biologia molecular - sbbq. Brasil.
  204. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2005. Recent developments in the biomedical applications of "in vivo" rna interference. In: Xxxiv reunião anual da sociedade brasileira de bioquímica e biologia molecular - sbbq. Brasil.
  205. Life Sciences Genetics
    Iara Leda Brandão De ALMEIDA; Adriana BORTOLAI; Catarina A GUIMARÃES; Ecila P M OLIVIEIRA; Simone R V HAGE et al. 2005. Absence of the 22q11.2 deletion syndrome in patients with polymicrogyria. In: Xvii congresso brasileiro de genética clínica. Brasil.
  206. Life Sciences Genetics
    Danilo Vilela VIANA; Iscia Teresinha Lopes CENDES; Carmen Silvia Passos LIMA; Juvenal Ricardo Navarro GOES; Cláudio Saddy Rodrigues COY et al. 2005. História familial de câncer nos pacientes com diagnóstico de câncer de cólon e reto no hospital de clínicas da unicamp. In: Xvii congresso brasileiro de genética clínica. Brasil.
  207. Health Sciences Pediatrics, Perinatology and Child Health
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Rejane Scolari Resende PAIVA; Anamarli NUCCI; Iscia Teresinha Lopes CENDES. 2005. Apresentação incomum em uma família com doença de machado-joseph. In: V congresso paulista de neurologia - ii congresso paulista de cefaléia - ii simpósio de atualização em enxaqueca e vii reunião paulista de neurofisiologia clínica (nfc) de são paulo. Brasil.
  208. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2005. Avanços na genética das doenças neurológicas. In: V congresso paulista de neurologia - ii congresso paulista de cefaléia - ii simpósio de atualização em enxaqueca e vii reunião paulista de neurofisiologia clínica (nfc) de são paulo. Brasil.
  209. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2005. Doenças neurodegenerativas causadas pela expansão de poliglutaminas (poliq). In: V congresso paulista de neurologia - ii congresso paulista de cefaléia - ii simpósio de atualização em enxaqueca e vii reunião paulista de neurofisiologia clínica (nfc) de são paulo. Brasil.
  210. Health Sciences Medicine (miscellaneous)
    Maria Do Carmo De Souza RODRIGUES; Fábio Rossi TORRES; A R FERNANDES; Lucia MORAES; M J CAMILO et al. 2005. Esquizencefalia - ausência de correlação entre quadro clínico/ extensão de fendas e associação das fendas e associação com outras anomalias cerebrais. In: Xvii congresso brasileiro de genética clínica. Brasil.
  211. Social Sciences & Humanities Psychology (miscellaneous)
    Maria Do Carmo De Souza RODRIGUES; Fábio Rossi TORRES; Alexandre R FERNANDES; Lucia MORAES; M J CAMILO et al. 2005. Esquizencefalia como parte de anomalia complexa do snc - relato de um caso. In: Xvii congresso brasileiro de genética clínica. Brasil.
  212. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES. 2005. Genética das epilepsias. In: V congresso paulista de neurologia - ii congresso paulista de cefaléia - ii simpósio de atualização em enxaqueca e vii reunião paulista de neurofisiologia clínica (nfc) de são paulo. Brasil.
  213. Life Sciences Neurology
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Rejane Scolari Resende PAIVA; Iscia Teresinha Lopes CENDES. 2005. Paraparesia espástica hereditária com hipoplasia de corpo caloso: uma série de pacientes brasileiros. In: V congresso paulista de neurologia - ii congresso paulista de cefaléia - ii simpósio de atualização em enxaqueca e vii reunião paulista de neurofisiologia clínica (nfc) de são paulo. Brasil.
  214. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 2005. Síndromes epilépticas geneticamente determinadas: aspectos clínicos e moleculares. In: V congresso paulista de neurologia - ii congresso paulista de cefaléia - ii simpósio de atualização em enxaqueca e vii reunião paulista de neurofisiologia clínica (nfc) de são paulo. Brasil.
  215. Life Sciences Neurology
    Fernando CENDES; Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2005. Epilepsy with generalized tonic-clonic seizures only: clinical and eeg features. In: 57th annual meeting of the american academy of neurology. Estados Unidos.
  216. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2005. Mri in idiopathic generalized epilepsy: is it necessary?. In: 57th annual meeting of the american academy of neurology. Estados Unidos.
  217. Health Sciences Neurology (clinical)
    Susana Barreto MORY; Li Li MIN; Iscia Teresinha Lopes CENDES; Marilisa Mantovani GUERREIRO; Carlos Alberto Mantovani GUERREIRO et al. 2005. Mri texture analysis in juvenile myclonic epilepsy. In: 57th annual meeting of the american academy of neurology. Estados Unidos.
  218. Health Sciences Neurology (clinical)
    Fernando CENDES; Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2005. Mri voxel-based-morphometry in families with idiopathic generalized epilepsy. In: 57th annual meeting of the american academy of neurology. Estados Unidos.
  219. Life Sciences Neuroscience (miscellaneous)
    Rodrigo SECOLIN; R G M FERREIRA; Cláudia V Maurer MORELLI; Neide F SANTOS; Eliane KOBAYASHI et al. 2004. Complex segregation analysis in familial mesial temporal lobe epilepsy (fmtle). In: Annual meeting of the american epilepsy society. Estados Unidos.
  220. Life Sciences Neurology
    Camila Fernanda LOPES; Fernando CENDES; Maria Augusta S MONTENEGRO; Ana Maria S G PIOVESANA; Fábio Rossi TORRES et al. 2004. Epileptic features of patients with unilateral and bilateral schizencephaly. In: Annual meeting of the american epilepsy society. Estados Unidos.
  221. Health Sciences Neurology (clinical)
    Eliane KOBAYASHI; Simone APPENZELLER; Susana Barreto MORY; Li Li MIN; Iscia Teresinha Lopes CENDES et al. 2004. Hippocampal 1h mrs findings in patients familial mesial temporal lobe epilepsy. In: Annual meeting of the american epilesy society. Estados Unidos.
  222. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Susana Barreto MORY; Patrícia Aline Oliveira RIBEIRO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Mri volumetry of the thalamus in patients with juvenile myoclonic epilepsy. In: Annual meeting of the american epilesy society. Estados Unidos.
  223. Health Sciences Genetics (clinical)
    Maria Cristina Cabral GARCIA; Celso Eduardo BENEDETTI; C L P OLIVEIRA; P R KUSER; G NESHICH et al. 2004. Human ataxin-3 structural analysis: preliminary data. In: 54th annual meeting of the american society of human genetics. Canadá.
  224. Life Sciences Molecular Biology
    Mariângela GRIPPO; Tiago Campos PEREIRA; Rovilson GIGLIOLI; Iscia Teresinha Lopes CENDES. 2004. In vitro rna interference against mhv-3 vírus. In: 54th annual meeting of the american society of human genetics. Canadá.
  225. Life Sciences Genetics
    Cláudia V Maurer MORELLI; Neide F SANTOS; Rodrigo SECOLIN; Eliane KOBAYASHI; Fernando CENDES et al. 2004. Linkage study of the candidate gene scn2a1 in familial mesial temporal lobe epilepsy (fmtle). In: 54th annual meeting of the american society of human genetics. Canadá.
  226. Life Sciences Parasitology
    Vinícius D Avila Bittencourt PASCHOAL; Tiago Campos PEREIRA; Ivan Godoy MAIA; Luis Augusto MAGALHÃES; Eliana M Zanotti MAGALHÃES et al. 2004. Rna interference against a parasitic infection. In: 54th annual meeting of the american society of human genetics. Canadá.
  227. Health Sciences Neurology (clinical)
    Patrícia Aline Oliveira RIBEIRO; Vinícius D Avila Bittencourt PASCHOAL; Luiz Eduardo BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2004. Searching for mutations in the efhc1 gene in patients with juvenile myoclonic epilepsy. In: 54th annual meeting of the american society of human genetics. Canadá.
  228. Life Sciences Neuroscience (miscellaneous)
    Tiago Campos PEREIRA; Ivan Godoy MAIA; Mariângela GRIPPO; Rovilson GIGLIOLI; Iscia Teresinha Lopes CENDES. 2004. Silencing of mecp2 in adult mice through rna. In: 54th annual meeting of the american society of human genetics. Canadá.
  229. Life Sciences Genetics
    Rodrigo SECOLIN; R G M FERREIRA; Cláudia V Maurer MORELLI; Neide F SANTOS; Eliane KOBAYASHI et al. 2004. Strong evidence of a major gene with mendelian transmission involved in familial mesial temporal lobe epilepsy (fmtle). In: 54th annual meeting of the american society of human genetics. Canadá.
  230. Health Sciences Medicine (miscellaneous)
    Rodrigo SECOLIN; R G M FERREIRA; Cláudia V Maurer MORELLI; Neide F SANTOS; Eliane KOBAYASHI et al. 2004. Análise de segregação complexa em famílias com epilepsia de lobo temporal mesial familiar. In: Xii congresso interno de iniciação científica da unicamp. Brasil.
  231. Life Sciences Neuroscience (miscellaneous)
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO et al. 2004. Estudo molecular de pacientes com distúrbio do desenvolvimento cortical. In: Xii congresso interno de iniciação científica da unicamp. Brasil.
  232. Life Sciences Neurology
    Rafael B MARCHESINI; Cláudia V Maurer MORELLI; Neide F SANTOS; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2004. Estudos de ligação no cromossomo 3 em região candidata para epilepsia do lobo temporal mesial familiar (eltmf). In: Xii congresso interno de iniciação científica da unicamp. Brasil.
  233. Life Sciences Genetics
    Émerson Salvador De Souza FRANÇA; M S SILVA; Iscia Teresinha Lopes CENDES. 2004. Investigação do sítio polimórfico ccg no gene hd na população brasileira. In: Xii congresso interno de iniciação científica da unicamp. Brasil.
  234. Life Sciences Animal Science and Zoology
    Vinícius D Avila Bittencourt PASCHOAL; Carlos Henrique TONHATTI; Tiago Campos PEREIRA; Ivan Godoy MAIA; Eneida De PAULA et al. 2004. Silenciamento in vitro de um gene essencial de s. mansoni. In: Xii congresso interno de iniciação científica da unicamp. Brasil.
  235. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Kalinca Patrícia Marengo SANTOS; Míriam Gisele Gasparotto CONTESSOTTO; Maria Cristina Cabral GARCIA; Iscia Teresinha Lopes CENDES. 2004. Análise molecular da proteína ataxina 1. In: 50º congresso brasileiro de genética. Brasil.
  236. Life Sciences Parasitology
    Mariângela GRIPPO; Tiago Campos PEREIRA; Rovilson GIGLIOLI; Iscia Teresinha Lopes CENDES. 2004. Avaliação in vitro da técnica "interferência por rna" no combate ao vírus mhv-3. In: 50º congresso brasileiro de genética. Brasil.
  237. Life Sciences Genetics
    Rafael B MARCHESINI; Cláudia V Maurer MORELLI; Neide F SANTOS; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2004. Estudo de ligação e análise de polimorfismos do tipo snps em região candidata no cromossomo 3 em famílias com epilepsia do lobo temporal mesial. In: 50º congresso brasileiro de genética. Brasil.
  238. Health Sciences Medicine (miscellaneous)
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO et al. 2004. Estudo de mutações em um grupo de pacientes com distúrbio do desenvolvimento cortical. In: 50º congresso brasileiro de genética. Brasil.
  239. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Daniela Medeiros De CASTRO; Flávia C NERY; Maria Cristina Cabral GARCIA; J KOBARG; Iscia Teresinha Lopes CENDES. 2004. Identificação de proteínas ligantes à ataxina-3 através do sistema de duplo híbrido. In: 50º congresso brasileiro de genética. Brasil.
  240. Life Sciences Genetics
    Émerson Salvador De Souza FRANÇA; Marilsa Santos SILVA; Iscia Teresinha Lopes CENDES. 2004. Investigação do sítio polimórfico ccg no gene hd na população brasileira. In: 50º congresso brasileiro de genética. Brasil.
  241. Life Sciences Genetics
    Tiago Campos PEREIRA; Ivan Godoy MAIA; Mariângela GRIPPO; Rovilson GIGLIOLI; Iscia Teresinha Lopes CENDES. 2004. Rna interference of mecp2 in adult mice does not lead to stereotyped forelimb movements. In: 50º congresso brasileiro de genética. Brasil.
  242. Life Sciences Neuroscience (miscellaneous)
    Maria Do Carmo Martins OLIVEIRA; R G M FERREIRA; Henrique KRIGER; Paulo DALGALARRONDO; Cem BANZATO et al. 2004. Análise de segregação em famílias com transtorno afetivo bipolar. In: Xvi congresso brasileiro de genética clínica. Brasil.
  243. Health Sciences Genetics (clinical)
    Maria Do Carmo De Souza RODRIGUES; Fábio Rossi TORRES; A L G MARIANTE; R ZLOT; V L MOURA et al. 2004. Ausência de mutações no gene homeobox emx2 em 33 pacientes portadores de esquizencefalia. In: Xvi congresso brasileiro de genética clínica. Brasil.
  244. Social Sciences & Humanities Psychology (miscellaneous)
    Rejane Scolari Resende PAIVA; Marilza Santos SILVA; Iscia Teresinha Lopes CENDES. 2004. O perfil psicossocial dos indivíduos interessados no teste preditivo para a doença de huntington e ataxias espinocerebelares. In: Xvi congresso brasileiro de genética clínica. Brasil.
  245. Life Sciences Genetics
    José Paulo Cabral De VASCONCELLOS; R B SCHIMITI; V P COSTA; Norisvaldo Cesar BRESSANIM; Fernando Ferreira COSTA et al. 2004. Pro59his: a novel mutation in the gja1 gene in a brazilian family with oculodentodigitaldysplasia. In: Arvo 2004. Estados Unidos.
  246. Health Sciences Medicine (miscellaneous)
    Kalinca Patrícia MARENGO; Míriam Gisele G CONTESOTTO; Vanessa CAPPOVILLA; Tiago Campos PEREIRA; Iscia Teresinha Lopes CENDES. 2004. Análise estrutural da ataxina 1. In: Xiv reunião anual de usuários do lnls (rau). Brasil.
  247. Life Sciences Molecular Biology
    Maria Cristina Cabral GARCIA; Celso Eduardo BENEDETTI; Cristiano L P OLIVEIRA; Iris C TORRIANI; Iscia Teresinha Lopes CENDES. 2004. Structural studies of human ataxin-3. In: Xiv reunião anual de usuários do lnls (rau). Brasil.
  248. Life Sciences Neurology
    R SECOLIN; Nf SANTOS; Fr TORRES; E KOBAYASHI; Laf SARDINHA et al. 2003. Evidência de heterogeneidade clínica e genética para epilepsia de lobo temporal familial com sintomas auditivos. In: Iv congresso paulista de neurologia. Brasil.
  249. Life Sciences Genetics
    R MARCHESIN; Nf SANTOS; R SECOLIN; E KOBAYASHI; F CENDES et al. 2003. Avanços nos estudos genéticos na epilepsia de lobo temporal mesial familiar. In: Iv congresso paulista de neurologia. Brasil.
  250. Health Sciences Medicine (miscellaneous)
    Rsr PAIVA; Iscia Teresinha Lopes CENDES. 2003. A opinião dos profissionais de saúde sobre testes moleculares para a doença de huntington e as ataxias espinocerebelares. In: Iv congresso paulista de neurologia. Brasil.
  251. Life Sciences Neuroscience (miscellaneous)
    Mc OLIVEIRA; P DALGALARRONDO; Cem BANZATO; Mfr ROSA; Ms SILVA et al. 2003. Estudo de famílias de indivíduos com transtorno afetivo bipolar. In: Iv congresso paulista de neurologia. Brasil.
  252. Life Sciences Neurology
    Pa RIBEIRO; V VASCONSELOS; Nf SANTOS; F CENDES; Iscia Teresinha Lopes CENDES. 2003. Epilepsia mioclônica juvenil e outras formas de epilepsia generalizada idiopática não estão relacionadas ao gene gabra1. In: Iv congresso paulista de neurologia. Brasil.
  253. Health Sciences Speech and Hearing
    Fr TORRES; Ap Marquesde FARIA; F CENDES; Iscia Teresinha Lopes CENDES. 2003. Lissencefalia clássica: uma nova mutação missense. In: Xv congresso brasileiro de genética clínica. Brasil.
  254. Life Sciences Neuroscience (miscellaneous)
    Mc OLIVEIRA; P DALGALARRONDO; Cem BANZATO; Mfr ROSA; Ms SILVA et al. 2003. Transtorno afetivo bipolar familiar: caracterização genético-clínica. In: Xv congresso brasileiro de genética clínica. Brasil.
  255. Social Sciences & Humanities Psychology (miscellaneous)
    Iscia Teresinha Lopes CENDES; Mfr ROSA. 2003. A percepção do sujeito de pesquisa sobre o termo de consentimento livre e esclarecido. In: Xv congresso brasileiro de genética clínica. Brasil.
  256. Life Sciences Neurology
    Maria Isabel C R MORAIS; F CENDES; Marilisa M GUERREIRO; Luciano QUEIROZ; Anamarli NUCCI et al. 2003. Protocolo clínico e molecular para avaliação de pacientes com epilepsia mioclônica progressiva. In: Iv congresso paulista de neurologia. Brasil.
  257. Life Sciences Immunology and Microbiology (miscellaneous)
    Tiago CAMPOSPEREIRA; Ivan G MAIA; Luis Augusto MAGALHÃES; Eliana ZANOTTIMAGALHÃES; Iscia Teresinha Lopes CENDES. 2003. Rna interference (rnai) against a parasitic infection. In: 49 congresso nacional de genética. Brasil.
  258. Health Sciences Medicine (miscellaneous)
    Maria Cristina Cabral GARCIA; Celso Eduardo BENEDETTI; Cristiano L P OLIVEIRA; Iris C L TORRIANI; Iscia Teresinha Lopes CENDES. 2003. Análise estrutural da ataxina 3. In: 49 congresso nacional de genética. Brasil.
  259. Life Sciences Neuroscience (miscellaneous)
    Rodrigo SECOLIN; Neide F SANTOS; Eliane KOBAYASHI; Fábio Rossi TORRES; Luiz A C SARDINHA et al. 2003. Progressos nos estudos de ligação genética em famílias brasileiras com epilepsia de lobo temporal com sintomas auditivos. In: 49 congresso nacional de genética. Brasil.
  260. Life Sciences Neuroscience (miscellaneous)
    Marilsa Santos SILVA; Anderson TAVARES; Heloisa Helena RUOCCO; Iscia Teresinha Lopes CENDES. 2003. Expansão cag na doença de huntington. In: 49 congresso nacional de genética. Brasil.
  261. Life Sciences Genetics
    Vanessa CAPPOVILA; Míriam Gisele Gasparotto CONTESSOTTO; Maria Cristina Cabral GARCIA; Kalinca MARENGOSANTOS; Iscia Teresinha Lopes CENDES. 2003. Análise estrutural da proteína ataxina 7. In: 49 congresso nacional de genética. Brasil.
  262. Health Sciences Medicine (miscellaneous)
    Patrícia Aline O RIBEIRO; Vinícius D Avila Bittencourt PASCHOAL; Luis Gg BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2003. Estudos de ligação e associação do locus 6p21 em epilepsias generalizadas idiopáticas. In: 49 congresso nacional de genética. Brasil.
  263. Health Sciences Neurology (clinical)
    Rafael B MARCHESINI; Neide F SANTOS; Cláudia MAURERMORELLI; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2003. Refinamento da região candidata no cromossomo 3 em famílias com epilepsia de lobo temporal mesial. In: 49 congresso nacional de genética. Brasil.
  264. Life Sciences Neurology
    Rafael B MARCHESINI; Neide F SANTOS; Cláudia V MAURERMORELLI; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2003. Refinamento da região candidata no cromossomo 3 em famílias com epilepsia do lobo temporal mesial (eltmf). In: Xi congresso interno de iniciação científica da unicamp. Brasil.
  265. Life Sciences Neuroscience (miscellaneous)
    Rodrigo SECOLIN; Neide F SANTOS; Eliane KOBAYASHI; Fábio Rossi TORRES; Luis A C SARDINHA et al. 2003. Uma nova mutação para epilepsia do lobo temporal familial com sintomas auditivos (eltfsa). In: Xi congresso interno de iniciação científica da unicamp. Brasil.
  266. Life Sciences Genetics
    Vanessa CAPPOVILA; Iscia Teresinha Lopes CENDES. 2003. Análise estrutural da proteína ataxina 7 normal. In: Xi congresso interno de iniciação científica da unicamp. Brasil.
  267. Life Sciences Neurology
    Vnícius D B PASCOAL; Patrícia Aline O RIBEIRO; Luiz G G BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2003. Análise de ligação e associação de um locus candidato no cromossomo 6p21 em pacientes com epilepsia mioclônica juvenil (emj). In: Xi congresso interno de iniciação científica da unicamp. Brasil.
  268. Health Sciences Medicine (miscellaneous)
    Rodrigo SECOLIN; Neide F SANTOS; Eliane KOBAYASHI; Fábio Rossi TORRES; Luiz A F SARDINHA et al. 2003. Uma nova mutação para epilepsia de lobo temporal familial com sintomas auditivos (eltfsa). In: 6 congresso aberto dos estudantes de biologia da unicamp. Brasil.
  269. Life Sciences Genetics
    Rafael B MARCHESINI; Neide F SANTOS; Cláudia V MAURERMORELLI; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2003. Indícios de ligação em região candidata do cromossomo 3 em famílias com epilepsia do lobo temporal mesial familiar (eltmf). In: 6 congresso aberto dos estudantes de biologia da unicamp. Brasil.
  270. Life Sciences Genetics
    Vinícius D Avila P BITENCOURT; Patrícia Aline O RIBEIRO; Luiz G G BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2003. Análise de ligação e associação de um locus candidato no cromossomo 6p21. In: 6 congresso aberto dos estudantes de biologia da unicamp. Brasil.
  271. Life Sciences Neuroscience (miscellaneous)
    Giselle Coelho Resende CASELATO; Eliane KOBAYASHI; Leonardo BONILHA; Gabriela CASTELLATO; Ares Hawatha RIGAS et al. 2003. Análise de textura hipocampal em pacientes com epilepsia de lobo temporal mesial familiar. In: Iv congresso paulista de neurologia. Brasil.
  272. Life Sciences Neuroscience (miscellaneous)
    Heloisa Helena RUOCCO; Marilza S SILVA; Tiago L LAURITO; Maura A VIANA; Elisabeth M A B QUAGLIATO et al. 2003. Quantificação da atrofia do caudato e putamen por rnm volumétrica em pacientes com doença de huntington. relação entre repetições do cag expandido e idade de início. In: Iv congresso paulista de neurologia. Brasil.
  273. Life Sciences Neuroscience (miscellaneous)
    Fábio Rossi TORRES; Maria Augusta MONTENEGRO; Maria Do Carmo RODRUIGUES; Ana Maria PIOVESANA; Juan Clinton LLERENA et al. 2003. Estudo molecular em uma amostra de pacientes com desordens do desenvolvimento cortical. In: Iv congresso paulista de neurologia. Brasil.
  274. Life Sciences Neurology
    Luiz Eduardo BETTING; Patríca Aline O RIBEIRO; Suzana B MORY; Li Li MIN; Carlos A M GUERREIRO et al. 2003. Fatores associados ao desencadeamento de crises em epilepsia generalizada idiopática. In: Iv congresso paulista de neurologia. Brasil.
  275. Social Sciences & Humanities Education
    Fernanda Ribeiro ROSA; Rejane Scolari Resende PAIVA; Iscia Teresinha Lopes CENDES. 2002. A experiência brasileira da unicamp com programas de testes preditivos. In: Encontro sobre aspectos psicossociais e éticos dos testes genéticos:doenças neurológicas de início tardio e cancros hereditários. Portugal.
  276. Life Sciences Neurology
    Laurito TL; Lima E Silva T; Silva MS; Rosa APF; Bertuzzo CS et al. 2002. Diagnóstico molecular da doença de huntington em uma amostra da população brasileira: uma experiência de 5 anos. In: 14° congresso brasileiro de genética clínica. Brasil.
  277. Life Sciences Neuroscience (miscellaneous)
    Brandão Almeida IL; Laurito TL; Costa Gomes MD; Pauxis S; Low CS et al. 2002. Doença de huntington na adolescência: o valor da história familial. In: 14° congresso brasileiro de genética clínica. Brasil.
  278. Life Sciences Neuroscience (miscellaneous)
    Rocha JJ; Camargo AA; Silva RLA; Iscia Teresinha Lopes CENDES; Simpson AJG. 2002. Searching for the von hippel-lindau disease (vhl): two important differential diagnoses. In: 14° congresso brasileiro de genética clínica. Brasil.
  279. Life Sciences Genetics
    Laurito TL; Lima E Silva T; Silva MS; Rosa APF; Iscia Teresinha Lopes CENDES. 2002. Diagnóstico molecular da doença de huntington em uma amostra da população brasileira: uma experiência de 5 anos. In: Xvii reunião anual da federação de sociedades de biologia experimental. Brasil.
  280. Life Sciences Genetics
    Rosa APF; Silva MS; Laurito TL; Iscia Teresinha Lopes CENDES. 2002. Análise molecular em pacientes com ataxia de friedreich. In: X congresso interno de iniciação científica da unicamp. Brasil.
  281. Life Sciences Genetics
    Lima JP; Iscia Teresinha Lopes CENDES. 2002. Identificação das mutações do gene sod1 em pacientes brasileiros com esclerose lateral amiotrófica familial. In: X congresso interno de iniciação científica da unicamp. Brasil.
  282. Life Sciences Neurology
    Sessa RGG; Santos MS; Iscia Teresinha Lopes CENDES. 2002. Análise molecular em pacientes com ataxias espinocerebelares autossômicas dominantes. In: X congresso interno de iniciação científica da unicamp. Brasil.
  283. Life Sciences Neurology
    Laurito TL; Lima E Silva T; Silva MS; Rosa APF; Bertusso CS et al. 2002. Diagnóstico molecular da doença de huntington em uma amostra da população brasileira: uma experiência de 5 anos. In: X congresso interno de iniciação científica da unicamp. Brasil.
  284. Health Sciences Neurology (clinical)
    E KOBAYASHI; N F SANTOS; R SECOLIN; S C SOUSA; C A M GUERREIRO et al. 2001. Epilepsia de lobo temporal mesial familiar: uma síndrome frequente mas pouco reconhecida. In: Congresso brasileiro de genética clínica. Brasil.
  285. Health Sciences Genetics (clinical)
    C E STEINER; M E R CAMARGO; D FACCHIN; A GEDEON; J C MULLEY et al. 2001. Comparação entre o uso das técnicas de citogenética; pcr e southern blotting no diagnóstico da síndrome do cromossomo x-frágil. In: Congresso brasileiro de genética clínica. Brasil.
  286. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; M M GERREIRO; Iscia Teresinha Lopes CENDES; F CENDES. 2001. Relevância dos fatores genéticos e pré-natais nas diferentes formas de malformações do desenvolvimento cortical. In: Congresso brasileiro de genética clínica. Brasil.
  287. Life Sciences Genetics
    João Paulo S Nogueira LIMA; D FACCHIN; M S SILVA; H G SERRA; H C A SILVA et al. 2001. Identificação das mutações do gene sod1 em pacientes brasileiros com esclerose lateral amiotrófica familial. In: Congresso brasileiro de genética clínica. Brasil.
  288. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2001. Desenvolvimento-maturação cerebral normal e patológica: genética molecular. In: I reunião do grupo comciemte (comissão científica metodológica e tecnológica. Brasil.
  289. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES. 2001. Epilepsias temporais familiais. In: Ii curso internacional : avances en epilepsias del niño y el adolecescente. Chile.
  290. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2001. Genética das epilepsias: estado atual do conhecimento. In: Ii curso internacional : avances en epilepsias del niño y el adolecescente. Chile.
  291. Life Sciences Neurology
    N F SANTOS; S C SOUSA; E KOBAYASHI; F R TORRES; L A F SARDINHA et al. 2001. Searching for genes predisposing to idiopathic partial epilepsy syndromes. In: Brazilian international genome conference. Brasil.
  292. Health Sciences Neurology (clinical)
    R S R PAIVA; F NORONHA; Iscia Teresinha Lopes CENDES. 2001. Atitudes frente aos testes moleculares em pacientes com doenças neurológicas de início tardio. In: Xii congresso brasileiro de genética clínica; iii simpósio luso-brasileiro de genética clínica. Brasil.
  293. Life Sciences Genetics
    D M De CASTRO; M I C R MORAIS; L S FERREIRA; M A MONTENEGRO; M M GUERREIRO et al. 2001. Mutação a3243g no mtdna como causa de epilepsia sintomática. In: Xii congresso brasileiro de genética clínica; iii simpósio luso-brasileiro de genética clínica. Brasil.
  294. Life Sciences Neurology
    D FACCHIN; E KOBAYASHI; F CENDES; C E STEINER; A Aa LEONE et al. 2001. Epilepsia generalizada secundária em pacientes com 46;xy;der(15)t(15-12)(q26-p13). In: Xii congresso brasileiro de genética clínica; iii simpósio luso-brasileiro de genética clínica. Brasil.
  295. Health Sciences Medicine (miscellaneous)
    C E STEINER; M E R CAMARGO; T C L SILVA; D FACCHIN; A P Marques De FARIA et al. 2001. Triagem para a mutação do fraxa pela técnica da pcr em uma amostra de indivíduos com distúrbios invasivos do desenvolvimento. In: Xii congresso brasileiro de genética clínica; iii simpósio luso-brasileiro de genética clínica. Brasil.
  296. Health Sciences Neurology (clinical)
    E KOBAYASHI; N F SANTOS; R SECOLIN; S C SOUSA; C A M GUERREIRO et al. 2001. Epilepsia de lobo temporal mesial familiar: uma síndrome frequente mas pouco reconhecida. In: 13° congresso brasileiro de genética clínica. Brasil.
  297. Health Sciences Genetics (clinical)
    C E STEINER; M E R CAMARGO; D FACCHIN; A GEDEON; J C MULLEY et al. 2001. Comparação entre o uso das técnicas de citogenética; pcr e southern blotting no diagnóstico da síndrome do cromossomo x-frágil. In: 13° congresso brasileiro de genética clínica. Brasil.
  298. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES. 2001. Relevância dos fatores genéticos e pré-natais nas diferentes formas de malformações do desenvolvimento cortical. In: 13° congresso brasileiro de genética clínica. Brasil.
  299. Life Sciences Genetics
    J P S N LIMA; D FACCHIN; M S SILVA; H G SERRA; H C A SILVA et al. 2001. Identificação das mutações do gene sod1 em pacientes brasileiros com esclerose lateral amiotrófica familial. In: 13° congresso brasileiro de genética clínica. Brasil.
  300. Life Sciences Genetics
    J P S N LIMA; D FACCHIN; M S SILVA; H G SERRA; H C A SILVA et al. 2001. Identificação das mutações do gene sod1 em pacientes brasileiros com esclerose lateral amiotrófica familial. In: Ix congresso interno de iniciação científica da unicamp. Brasil.
  301. Life Sciences Neurology
    R SECOLIN; F R TORRES; N F SANTOS; E KOBAYASHI; L A F SARDINHA et al. 2001. Epilepsia de lobo temporal com sintomas auditivos: evidência de ligação no cromossomo 10q. In: 47° congresso nacional de genética. Brasil.
  302. Life Sciences Neuroscience (miscellaneous)
    F R TORRES; M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES. 2001. Estudo de mutações em genes responsáveis por diferentes desordens de desenvolvimento cortical. In: 47° congresso nacional de genética. Brasil.
  303. Health Sciences Medicine (miscellaneous)
    M E R CAMARGO; Iscia Teresinha Lopes CENDES; A P Marques De FARIA. 2001. Análise da mutação fraxa pelas técnicas da pcr e southern blot; em indivíduos do sexo masculino com deficiência mental de etiologia não esclarecida. In: 47° congresso nacional de genética. Brasil.
  304. Life Sciences Genetics
    P M VIEIRA; M I C R MORAIS; D M CASTRO; T AMARAL; J A R GONTIJO et al. 2001. Epilepsia mioclônica progressiva associada a lipomas gigantes em paciente portadora da mutação a8344g no mtdna. In: 47° congresso nacional de genética. Brasil.
  305. Life Sciences Genetics
    D M De CASTRO; M I C R MORAIS; L De DEUS; P M VIEIRA; A NUCCI et al. 2001. Mutação g11778a no mtdna como causa de ataxia; neuropatia periférica e oftalmoplegia. In: 47° congresso nacional de genética. Brasil.
  306. Health Sciences Neurology (clinical)
    R S R PAIVA; Iscia Teresinha Lopes CENDES. 2001. Teste preditivo para doenças neurodegenerativas de início tardio: a visão dos profissionais de saúde. In: 47° congresso nacional de genética. Brasil.
  307. Life Sciences Neuroscience (miscellaneous)
    R S R PAIVA; Iscia Teresinha Lopes CENDES. 2001. Teste molecular diagnóstico em pacientes com doenças neurodegenerativas de início tardio: a visão do paciente. In: 47° congresso nacional de genética. Brasil.
  308. Health Sciences Medicine (miscellaneous)
    Silva HCA; Serra HG; Silva MS; Lima JPSN; Callegaro D et al. 2001. Molecular analysis in the differential diagnosis of kennedy´s disease. In: Amyotrophic lateral sclerosis and other motor neuron disorders. Estados Unidos.
  309. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES. 2000. Particularidades do tratamento da epilepsia refratária na mulher: gestação e teratogenicidade. In: Curso avanços no diagnóstico e terapêutica das epilepsias refratárias: uma abordagem teórico-prática. Brasil.
  310. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES. 2000. A identificação de genes que predispõem a doenças neurológicas. In: Xix congresso brasileiro de neurologia. Brasil.
  311. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2000. O aconselhamento genético na prática neurológica. In: Xix congresso brasileiro de neurologia. Brasil.
  312. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES. 2000. Genética das doenças neurodegenerativas do adulto. In: Xix congresso brasileiro de neurologia. Brasil.
  313. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; W FERNANDES; L S FERREIRA et al. 2000. Fatores genéticos e ambientais na etiologia das disgenesias corticais. In: Primer congreso latinoamericano de epilepsia. Chile.
  314. Life Sciences Neurology
    E KOBAYASHI; D FACCHIN; F CENDES; C E STEINER; Andréa A Alves LEONE et al. 2000. Secondary generalized epilepsy in patients with karyotype 46xy; der (15t) (15-12) (q26-p13). In: Primer congreso latinoamericano de epilepsia. Chile.
  315. Life Sciences Neuroscience (miscellaneous)
    S C SOUSA; E KOBAYASHI; F CENDES; Iscia Teresinha Lopes CENDES. 2000. Familial mesial temporal lobe epilepsy (tle) do not map to chromosome 10q. In: Primer congreso latinoamericano de epilepsia. Chile.
  316. Life Sciences Neurology
    N F SANTOS; S C SOUSA; E KOBAYASHI; F R TORRES; L A F SARDINHA et al. 2000. Searching for genes predisposing to idiopathic partial epilepsy syndromes. In: Brazilian international genome conference. Brasil.
  317. Life Sciences Genetics
    M I C R MORAIS; D M CASTRO; L S FERREIRA; M A MONTENEGRO; M M GERREIRO et al. 2000. Mutação a3243g no mtdna como causa de epilepsia sintomática. In: Congresso da liga brasileira de epilepsia. Brasil.
  318. Health Sciences Genetics (clinical)
    D FACCHIN; S ANTONIUK; I BRUCK; J C COSTA; L JARDIM et al. 2000. Estudo de ligação na região xq28 em 25 famílias de pacientes com síndrome de rett. In: Congresso brasileiro de genética clínica. Brasil.
  319. Life Sciences Neuroscience (miscellaneous)
    R S R PAIVA; F NORONHA; Iscia Teresinha Lopes CENDES. 2000. Atitudes frente aos testes moleculares em pacientes com doenças neurológicas de início tardio. In: Congresso brasileiro de genética clínica. Brasil.
  320. Life Sciences Neurology
    D FACCHIN; E KOBAYASHI; F CENDES; C E STEINER; A A A LEONE et al. 2000. Epilepsia generalizada secundária em pacientes com 46;xy;der(15)t(15-12)(q26-p13). In: Congresso brasileiro de genética clínica. Brasil.
  321. Health Sciences Genetics (clinical)
    C E STEINER; M E R CAMARGO; T C L SILVA; D FACCHIN; A P MARQUESDEFARIA et al. 2000. Triagem para a mutação do fraxa pela técnica da pcr em uma amostra de indivíduos com distúrbios invasivos do desenvolvimento. In: Congresso brasileiro de genética clínica. Brasil.
  322. Health Sciences Psychiatry and Mental Health
    Iscia Teresinha Lopes CENDES. 2000. Doenças degenerativas. In: I workshop estudo da dinâmica cerebral normal e patológica. Brasil.
  323. Health Sciences Neurology (clinical)
    M A MONTENEGRO; M M GUERREIRO; L S FERREIRA; Iscia Teresinha Lopes CENDES; F CENDES et al. 2000. Malformations of cortical development: contribution of genetic and pre-natal events to its etiology. In: Eleventh international cleveland clinic - bethel epilepsy symposium. Estados Unidos.
  324. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES. 2000. Doenças degenerativas. In: I workshop estudo da dinâmica cerebral normal e patológica. Brasil.
  325. Health Sciences Genetics (clinical)
    D FACCHIN; S ANTONIUK; I BRUCK; J C COSTA; L JARDIM et al. 2000. Estudo de ligação na região xq28 em 25 famílias de pacientes com síndrome de rett. In: Xii congresso brasileiro de genética clínica; iii simpósio luso-brasileiro de genética clínica. Brasil.
  326. Life Sciences Neurology
    D FACCHIN; S A ANTONIUK; I BRUCK; Iscia Teresinha Lopes CENDES. 1999. Síndrome de rett:aspectos clínicos e moleculares. In: Congresso brasileiro de genética clínica. Brasil.
  327. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1999. Epilepsia na gravidez e amamentação: aspectos neurológicos. In: 48 congresso brasileiro de ginecologia e obstetrícia. Brasil.
  328. Health Sciences Neurology (clinical)
    E C ETCHEBEHERE; Iscia Teresinha Lopes CENDES; F CENDES; J PEREIRA; M LIMA et al. 1999. Spect cerebral na doença de machado-joseph. In: Congresso de la asociacion latinoamericana de sociedades de biologia y medicina nuclear. Argentina.
  329. Social Sciences & Humanities Communication
    Iscia Teresinha Lopes CENDES. 1998. Estudos de ligação ("linkage"). In: Xvii congresso brasileiro de neurologia. Brasil.
  330. Life Sciences Neuroscience (miscellaneous)
    I Lopes CENDES; Iscia Teresinha Lopes CENDES. 1998. Doenças neurodegenerativas causadas por expansão de trinucleotídeos. In: Xvii congresso brasileiro de neurologia. Brasil.
  331. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; E ATTIG; S BOSCH; M WAGNER et al. 1997. Molecular genetic characteristics and clinical-pathological correlations in spinocerebellar ataxia type 2 (sca2). In: International ataxia meeting. Canadá.
  332. Life Sciences Neurology
    T KLOCKGETHER; B EVERT; R LÜDTKE; B KRAMER; M ABELE et al. 1997. The natural history of degenerative ataxia: a retrospective study in 420 patients. In: International ataxia meeting. Canadá.
  333. Life Sciences Genetics
    C GASPAR; J GOTO; Iscia Teresinha Lopes CENDES; S HAYES; K ARVIDSSON et al. 1997. Different origins of mutation in machado-joseph disease patients. In: International ataxia meeting. Canadá.
  334. Life Sciences Genetics
    S HAYES; Iscia Teresinha Lopes CENDES; C FIGUEROA; C GASPAR; G A S M PULST. 1997. Haplotype analysis of a group of spinocerebellar ataxia type 2 (sca2) families. In: International ataxia meeting. Canadá.
  335. Life Sciences Genetics
    P MACIEL; C GASPAR; L GUIMARÃES; A DIAS; K ARVIDSON et al. 1997. Effect of the normal chromosome on the instability of the cag repeat in the mjd1 gene. In: International ataxia meeting. Canadá.
  336. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; H G A TEIVE; M E CALCAGNOTTO; J C Da COSTA; F CARDOSO et al. 1997. Frequency of the different mutations causing spinocerebellar ataxia (sca1; sca2; mjd/sca3 and drpla) in a large group of brazilian patients. In: International workshop on machado-joseph disease. Brasil.
  337. Life Sciences Genetics
    C E STEINER; W Pinto JÚNIOR; J A MACIEL; G A ROULEAU; Iscia Teresinha Lopes CENDES. 1997. Clinical and molecular characteristics of a brazilian family with spinocerebellar ataxia type 1 (sca1). In: International workshop on machado-joseph disease. Brasil.
  338. Life Sciences Genetics
    W O ARRUDA; S A PAROLIM; H A G TEIVE; Iscia Teresinha Lopes CENDES; G A ROULEAU et al. 1997. Sca2: the first diagnosed family in brazil. In: International workshop on machado-joseph disease. Brasil.
  339. Health Sciences Psychiatry and Mental Health
    Iscia Teresinha Lopes CENDES; E ANDERMANN; G A ROULEAU. 1997. Autosomal dominant spinocerebellar ataxias: what does the genotype have to do with the phenotype?. In: Neurology grand rounds. montreal neurological institute and hospital. Canadá.
  340. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; I SILVEIRA; C GASPAR; P MACIEL et al. 1996. Genotype versus phenotype: what have we learned with the molecular characterization of spinocerebellar ataxia type 1 (sca1) and machado-joseph disease (mjd/sca3). In: Update in neurogenetics 1996. world federation of neurology (wfn) neurogenetics research group meeting. Estados Unidos.
  341. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; I SILVEIRA; S KISH; J RADVANY et al. 1995. Frequency of spinocerebellar ataxia type 1; dentatorubropallidoluysian atrophy and machado-joseph disease mutations in a large group of spinocerebellar ataxia patients. In: Neurogenetics symposium; world federation of neurology. Estados Unidos.
  342. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; G A ROULEAU. 1995. Autosomal dominant spinocerebellar ataxias: clinical and molecular genetic aspects. In: Neurology grand rounds. montreal neurological institute and hospital. Canadá.
  343. Social Sciences & Humanities Linguistics and Language
    I SILVEIRA; P MACIEL; C GASPAR; Iscia Teresinha Lopes CENDES; E TWIST et al. 1994. Linkage studies in machado-joseph disease of non-portuguese ethnic background. In: Third machado-joseph disease workshop. Portugal.
  344. Health Sciences Neurology (clinical)
    E ANDERMANN; F ANDERMANN; S LEONBERG; S CARPENTER; Iscia Teresinha Lopes CENDES et al. 1994. Autosomal dominant progressive myoclonic epilepsy (pme): evidence for genetic heterogeneity in autosomal dominant kufs'disease. In: International neuronal ceroid lipofuscinosis workshop. Estados Unidos.
  345. Life Sciences Neurology
    I E SCHEFFER; K BHATIA; Iscia Teresinha Lopes CENDES; D FISH; C D MARSDEN et al. 1994. Autosomal dominant frontal lobe epilepsy. In: International cleveland clinic- bethel epilepsy symposium. Estados Unidos.
  346. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; E ATTIG; F CENDES; S BOSCH et al. 1994. Autosomal dominant spinocerebellar ataxia: an update on linkage studies of sca 2 families. In: Workshop on the molecular genetics of friedreich´s and dominant ataxias. Tunísia.
  347. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 1994. Genética das epilepsias: aspectos moleculares. In: Encontro da liga brasileira de epilepsia. Brasil.
  348. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; G A ROULEAU. 1994. Analysis of clinical and genetic heterogeneity in autosomal dominant spinocerebellar ataxia families of different ethnic background. In: 3rd machado joseph disease workshop. Portugal.
  349. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; G A ROULEAU. 1994. The genetics of the epilepsies. In: Neurology grand rounds; montreal neurological institute and hospital. Canadá.
  350. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; F ANDERMANN; J I COCHIUS; G A ROULEAU. 1994. Searching for epilepsy genes. In: Neurogenetics research group meeting; world federation of neurology. Canadá.
  351. Life Sciences Genetics
    E ANDERMANN; Iscia Teresinha Lopes CENDES; E ATTIG; F CENDES; J RADVANY et al. 1993. Clinical and genetic studies in dominantly inherited spinocerebellar ataxias (sca): analyses of clinical heterogeneity. In: International workshop on the molecular genetics of friedreich's and dominant ataxias. Itália.
  352. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; G A ROULEAU. 1993. Linkage analysis shows evidence for three different spinocerebellar ataxia (sca) loci. In: 4th annual student research day; the montreal general hospital research institute. Canadá.
  353. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; G A ROULEAU. 1993. Clinical and genetic heterogeneity in dominantly inherited spinocerebellar ataxias. In: World federation of neurology; neurogenetics research group meeting. Estados Unidos.
  354. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; G A ROULEAU. 1993. Clinical and genetic heterogeneity in dominantly inherited spinocerebellar ataxias. In: 35th annual fellow's day; montreal neurological institute and hospital. Canadá.
  355. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 1992. Dominant ataxia: clinical and molecular aspects. In: Mcgill genetics rounds. Canadá.
  356. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 1992. Dominant spinocerebellar ataxias: case presentation and review of classification. In: Service a clinical rounds; montreal neurological institute and hospital. Canadá.
  357. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 1992. Spinocerebellar ataxias project. In: Friedreich's ataxia group annual general meeting. Inglaterra.
  358. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; J RADVANY; G A ROULEAU. 1992. Linkage studies in spinocerebellar ataxia: evidence confirming genetic heterogeneity. In: Centre for human genetics; research day. Canadá.
  1. Life Sciences Neurology
    Mejía Granados Diana MARCELA; Villasana Salazar BENJAMÍN; Coan Ana CAROLINA; Rizzi LIARA; Balthazar Marcio Luiz FIGUEREDO et al. 2022. Gut microbiome in neuropsychiatric disorders. Arquivos de neuro-psiquiatria (online). 80, 192-207.
  2. Life Sciences Neuroscience (miscellaneous)
    Canto Amanda M; Godoi Alexandre B; Matos Alexandre H B; Geraldis Jaqueline C; Rogerio FABIO et al. 2022. Benchmarking the proteomic profile of animal models of mesial temporal epilepsy. Annals of clinical and translational neurology. 9, 454-467.
  3. Life Sciences Genetics
    Correia Costa Gabriela ROLDÃO; Sgardioli Ilária CRISTINA; Santos Ana Paula DOS; Araujo Tânia Kawasaki DE; Secolin RODRIGO et al. 2022. Increased runs of homozygosity in the autosomal genome of brazilian individuals with neurodevelopmental delay/intellectual disability and/or multiple congenital anomalies investigated by chromosomal microarray analysis. Genetics and molecular biology (online version). 45, e20200480-.
  4. Life Sciences Neurology
    Najm IMAD; Lal DENNIS; Alonso Vanegas MARIO; Fernando CENDES; Iscia Teresinha Lopes CENDES et al. 2022. The <scp>ilae</scp> consensus classification of focal cortical dysplasia: an update proposed by an ad hoc task force of the <scp>ilae</scp> diagnostic methods commission. Epilepsia. 63, 1899-1919.
  5. Life Sciences Neuroscience (miscellaneous)
    Machado João P D; Athie Maria C P; Matos Alexandre H B; Iscia Teresinha Lopes CENDES; Vieira André S. 2022. The transcriptome of rat hippocampal subfields. Ibro neuroscience reports. 13, 322-329.
  6. Life Sciences Neurology
    Van Loo Karen M J; Carvill Gemma L; Becker Albert J; Conboy KAREN; Goldman Alica M et al. 2022. Epigenetic genes and epilepsy - emerging mechanisms and clinical applications. Nature reviews neurology. 18, 530-543.
  7. Health Sciences Neurology (clinical)
    Vinicius D Avila Bitencourt PASCOAL; Marchesini R B; Athié M C P; Alexandre Hilário Berenguer De MATOS; Conte F F et al. 2022. Modulating expression of endogenous interleukin 1 beta in the acute phase of the pilocarpine model of epilepsy may change animal survival. Cellular and molecular neurobiology. 1, ahead of print-.
  8. Life Sciences Cell Biology
    Ignarro Raffaela SILVESTRE; Bombeiro André LUIS; Chiarotto Gabriela BORTOLANÇA; Cartarozzi Luciana POLITTI; Coser Lilian De OLIVEIRA et al. 2022. Interferon-beta induces major histocompatibility complex of class i (mhc-i) expression and a proinflammatory phenotype in cultivated human astrocytes. Differentiation. 128, 43-56.
  9. Health Sciences Neurology (clinical)
    Maurer Morelli Claudia V; De Vasconcellos Jaira F; Bruxel Estela M; Rocha Cristiane S; Do Canto Amanda M et al. 2022. Gene expression profile suggests different mechanisms underlying sporadic and familial mesial temporal lobe epilepsy. Experimental biology and medicine. 1, 153537022211266-.
  10. Health Sciences Neurology (clinical)
    Godoi Alexandre B; Do Canto Amanda M; Donatti AMANDA; Rosa Douglas C; Bruno Danielle C F et al. 2022. Circulating metabolites as biomarkers of disease in patients with mesial temporal lobe epilepsy. Metabolites. 12, 446-.
  11. Social Sciences & Humanities Anthropology
    Da Cruz Pedro Rodrigues SOUSA; Ananina GALINA; Secolin RODRIGO; Gil Da Silva Lopes Vera LÚCIA; Lima Carmen Silvia PASSOS et al. 2022. Demographic history differences between hispanics and brazilians imprint haplotype features. G3-genes genomes genetics. 12, 1-13.
  12. Life Sciences Neuroscience (miscellaneous)
    Aoyama Beatriz B; Zanetti Gabriel G; Dias Elayne V; Athié Maria C P; Iscia Teresinha Lopes CENDES et al. 2022. Transcriptomic analysis of dorsal and ventral subiculum after induction of acute seizures by electric stimulation of the perforant pathway in rats. Hippocampus. 32, 436-448.
  13. Life Sciences Neuroscience (miscellaneous)
    Ibanez LAURA; Heitsch LAURA; Carrera CATY; Farias Fabiana H G; Del Aguila Jorge L et al. 2022. Multi-ancestry gwas reveals excitotoxicity associated with outcome after ischaemic stroke. Brain. 145, 2394-2406.
  14. Health Sciences Neurology (clinical)
    Do Canto Amanda M; Donatti AMANDA; Geraldis Jaqueline C; Godoi Alexandre B; Da Rosa Douglas C et al. 2021. Neuroproteomics in epilepsy: what do we know so far?. Frontiers in molecular neuroscience. 13, Published onlin-.
  15. Life Sciences Genetics
    Secolin RODRIGO; De Araujo Tânia K; Gonsales Marina C; Rocha Cristiane S; Naslavsky MICHEL et al. 2021. Genetic variability in covid-19-related genes in the brazilian population. Human genome variations. 8, on line-9.
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    Santos Renato O; Secolin RODRIGO; Barbalho Patrícia G; Silva Alves Mariana S; Alvim Marina K M et al. 2021. Multidimensional approach assessing the role of interleukin 1 beta in mesial temporal lobe epilepsy. Frontiers in neurology. 12, e.690847-.
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    Secolin RODRIGO; Gonsales Marina C; Rocha Cristiane S; Naslavsky MICHEL; De Marco LUIZ et al. 2021. Exploring a region on chromosome 8p23.1 displaying positive selection signals in brazilian admixed populations: additional insights into predisposition to obesity and related disorders. Frontiers in genetics. 12, Published onlin-.
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    Kaibara Felipe S; De Araujo Tânia K; Araujo Patricia A O R A; Alvim Marina K M; Yasuda Clarissa L et al. 2021. Association analysis of candidate variants in admixed brazilian patients with genetic generalized epilepsies. Frontiers in genetics. 12, onlinePublished-.
  19. Life Sciences Neurology
    Pinto Wladimir Bocca Vieira De REZENDE; Salomão Rubens Paulo ARAÚJO; Bergamasco Nathália CABRAL; Da Cunha Ribas GUSTAVO; Da Graça Felipe FRANCO et al. 2021. Drpla: an unusual disease or an underestimated cause of ataxia in brazil?. Parkinsonism & related disorders. 92, 67-71.
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    Alvim Marina K M; Morita Sherman Marcia E; Yasuda Clarissa L; Rocha Natália P; Vieira Érica L et al. 2021. Inflammatory and neurotrophic factor plasma levels are related to epilepsy independently of etiology. Epilepsia. 62, 2385-2394.
  21. Life Sciences Neurology
    Prota JOANA; Rizzi LIARA; Bonadia LUCIANA; Souza Leonardo CRUZ; Caramelli PAULO et al. 2021. Slowly progressive behavioral frontotemporal dementia syndrome in a family co-segregating the c9orf</i> 72 expansion and a synaptophysin</i> mutation. Alzheimers & dementia. 1, *-.
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    Bruxel Estela M; Canto Amanda M; Bruno Danielle C F; Geraldis Jaqueline C; Iscia Teresinha Lopes CENDES. 2021. Multi-omic strategies applied to the study of pharmacoresistance in mesial temporal lobe epilepsy. Epilepsia open. 1, 1-27.
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    Stevelink REMI; Luykx Jurjen J; Lin Bochao D; Leu COSTIN; Smith Alexander W et al. 2021. Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations. Epilepsia. 62, 1518-1527.
  24. Life Sciences Neurology
    Blümcke INGMAR; Coras ROLAND; Busch Robyn M; Morita Sherman MARCIA; Lal DENNIS et al. 2021. Toward a better definition of focal cortical dysplasia: an iterative histopathological and genetic agreement trial. Epilepsia. 62, 1416-1428.
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    Charret Thiago S; Pereira Mariana T M; Pascoal Vinicius D B; Iscia Teresinha Lopes CENDES; Cristina Rheder Fagundes Pascoal AISLAN. 2021. Citral effects on the expression profile of brain-derived neurotrophic factor</i> and inflammatory cytokines in status epilepticus-induced rats using the lithium-pilocarpine model. Journal of medicinal food. 24, 916-924.
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    Bruxel Estela M; Bruno Danielle C F; Do Canto Amanda M; Geraldis Jaqueline C; Godoi Alexandre B et al. 2021. Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: clues into the underlying mechanisms leading to disease. Seizure-european journal of epilepsy. 1, 34-50.
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    Avansini Simoni H; Puppo FRANCESCA; Adams Jason W; Vieira Andre S; Coan Ana C et al. 2021. Junctional instability in neuroepithelium and network hyperexcitability in a focal cortical dysplasia human model. Brain. 145, 1962-1977.
  28. Physical Sciences Artificial Intelligence
    Cendes Lucas L; De Souza WELLITON; Iscia Teresinha Lopes CENDES; Carvalho Benilton S. 2020. Hpexome: an automated tool for processing whole-exome sequencing data. Softwarex. 11, 100478-10082.
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    Borges Murilo G; Rocha Cristiane S; Carvalho Benilton S; Iscia Teresinha Lopes CENDES. 2020. Methodological differences can affect sequencing depth with a possible impact on the accuracy of genetic diagnosis. Genetics and molecular biology (online version). 43, e20190270-.
  30. Life Sciences Cell Biology
    Baptista Letícia CARVALHO; Costa Maria LAURA; Surita Fernanda GARANHANI; Rocha Cristiane De SOUZA; Iscia Teresinha Lopes CENDES et al. 2020. Placental transcriptome profile of women with sickle cell disease reveals differentially expressed genes involved in migration; trophoblast differentiation and inflammation. Blood cells molecules and diseases. 84, 102458-.
  31. Life Sciences Genetics
    Gonçalves João Pedro NUNES; De Andrade Helen Maia TAVARES; Cintra Vívian PEDIGONE; Bonadia Luciana CARDOSO; Leoni Tauana BERNARDES et al. 2020. Cag repeats-≥-34 in ataxin-1 gene are associated with amyotrophic lateral sclerosis in a brazilian cohort. Journal of the neurological sciences. 414, 116842-.
  32. Health Sciences Medicine (miscellaneous)
    Katja KOBOW; Christopher A REID; Erwin A Van VLIET; Albert J BECKER; Gemma L CARVILL et al. 2020. Epigenetics explained: a topic 'primer' for the epilepsy community by the ilae genetics/epigenetics task force. Epileptic disorders : international epilepsy journal with videotape. 22, 127-141.
  33. Life Sciences Genetics
    Akçimen FULYA; Martins SANDRA; Liao CALWING; Bourassa Cynthia V; Catoire HÉLÈNE et al. 2020. Genome-wide association study identifies genetic factors that modify age at onset in machado-joseph disease. Aging-us. 12, 4742-4756.
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    Grasby Katrina L; Jahanshad NEDA; Painter Jodie N; Colodro Conde LUCÍA; Bralten JANITA et al. 2020. The genetic architecture of the human cerebral cortex. Science. 367, eaay6690-.
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    Do Canto Amanda M; Vieira André S; H B Matos ALEXANDRE; Carvalho Benilton S; Henning BARBARA et al. 2020. Laser microdissection-based microproteomics of the hippocampus of a rat epilepsy model reveals regional differences in protein abundances. Scientific reports. 10, 4412-.
  36. Life Sciences Molecular Biology
    Rosselli Murai Luciana K; Joseph Jophin G; Iscia Teresinha Lopes CENDES; Liu Allen P; Murai Marcelo J. 2020. The machado-joseph disease-associated form of ataxin-3 impacts dynamics of clathrin-coated pits. Cell biology international. 44, 1252-1259.
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    Bruno D C F; Amanda DONATTI; Martin M; Almeida V S; Geraldis J C et al. 2020. Circulating nucleic acids in the plasma and serum as potential biomarkers in neurological disorders. Brazilian journal of medical and biological research (on line). 53, 3-15.
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    Rocha Cristiane S; Secolin RODRIGO; Rodrigues Maíra R; Carvalho Benilton S; Iscia Teresinha Lopes CENDES. 2020. The brazilian initiative on precision medicine (bipmed): fostering genomic data-sharing of underrepresented populations. Npj genomic medicine. 5, 42-.
  39. Life Sciences Genetics
    Gonsales Marina C; Ribeiro Patrícia A O; Betting Luiz E; Alvim Marina K M; Guerreiro Carlos M et al. 2020. Revisiting the clinical impact of variants in efhc1 in patients with different phenotypes of genetic generalized epilepsy. Epilepsy & behavior. 112, 107469-.
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    Donatti AMANDA; Canto Amanda M; Godoi Alexandre B; Da Rosa Douglas C; Iscia Teresinha Lopes CENDES. 2020. Circulating metabolites as potential biomarkers for neurological disorders-metabolites in neurological disorders. Metabolites. 10, 389-.
  41. Health Sciences Neurology (clinical)
    Canto Amanda M; Matos Alexandre H B; Godoi Alexandre B; Vieira André S; Aoyama Beatriz B et al. 2020. Multi-omics analysis suggests enhanced epileptogenesis in the cornu ammonis</i> 3 of the pilocarpine model of mesial temporal lobe epilepsy. Hippocampus. 1, 1-18.
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    Franklin Gustavo L; Camargo Carlos Henrique F; Meira Alex T; Pavanelli Giovana M; Milano Sibele S et al. 2020. Is ataxia an underestimated symptom of huntington's disease?. Frontiers in neurology. 11, e-colection-.
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    Borges Murilo GUIMARÃES; Moraes Helena Tadiello DE; Rocha Cristiane De SOUZA; Iscia Teresinha Lopes CENDES. 2020. The impact of post-alignment processing procedures on whole-exome sequencing data. Genetics and molecular biology (online version). 43, onlinePublished-.
  44. Life Sciences Genetics
    Hofer EDITH; Roshchupkin Gennady V; Adams Hieab H H; Knol Maria J; Lin HONGHUANG et al. 2020. Genetic correlations and genome-wide associations of cortical structure in general population samples of 22;824 adults. Nature communications. 11, 4796-.
  45. Health Sciences Genetics (clinical)
    Ferreira Leslie ECKER; Secolin RODRIGO; Iscia Teresinha Lopes CENDES; Cabral Norberto LUIZ; De França Paulo Henrique CONDEIXA. 2019. Association and interaction of genetic variants with occurrence of ischemic stroke among brazilian patients. Gene. 8, 84-91.
  46. Health Sciences Genetics (clinical)
    Gonsales Marina C; Montenegro Maria AUGUSTA; Preto PAULA; Guerreiro Marilisa M; Coan Ana CAROLINA et al. 2019. Multimodal analysis of scn1a missense variants improves interpretation of clinically relevant variants in dravet syndrome. Frontiers in neurology. 10, article 289-.
  47. Life Sciences Genetics
    Peluzzo Thiago MAZZO; Bonadia Luciana CARDOSO; Donatti AMANDA; Molck Miriam COELHO; Jardim Laura BANNACH et al. 2019. Frequency and genetic profile of compound heterozygous friedreich?s ataxia patients¿the brazilian experience. Cerebellum. 18, 1143-1146.
  48. Life Sciences Genetics
    Rodrigues Peres Raquel M; S Carvalho BENILTON; Anurag MEENAKSHI; Lei Jonathan T; Conz LIVIA et al. 2019. Copy number alterations associated with clinical features in an underrepresented population with breast cancer. Molecular genetics & genomic medicine. 7, e750-.
  49. Health Sciences Radiology, Nuclear Medicine and Imaging
    De Carvalho Siqueira Gabriela QUEILA; Ananina GALINA; De Souza Bruno BATISTA; Borges Murilo GUIMARÃES; Ito Mirta TOMIE et al. 2019. Whole-exome sequencing indicates flg</i> 2 variant associated with leg ulcers in brazilian sickle cell anemia patients. Experimental biology and medicine. 244, 932-939.
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    Magalhães Pedro H M; Moraes Helena T; Athie Maria C P; Secolin RODRIGO; Iscia Teresinha Lopes CENDES. 2019. New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies. Epilepsy & behavior. 1, 106428-.
  51. Life Sciences Neuroscience (miscellaneous)
    Secolin RODRIGO; Mas Sandoval ALEX; Arauna Lara R; Torres Fábio R; De Araujo Tânia K et al. 2019. Distribution of local ancestry and evidence of adaptation in admixed populations. Scientific reports. 9, 13900-.
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    Avansini Simoni H; Torres Fábio R; Vieira André S; Dogini Danyella B; Rogerio FABIO et al. 2018. Dysregulation of neurog2</i> plays a key role in focal cortical dysplasia. Annals of neurology. 1, 1-.
  53. Life Sciences Cell Biology
    Facchini GUSTAVO; Ignarro Raffaela SILVESTRE; Rodrigues Silva ERIKA; Vieira André SCHWAMBACH; Iscia Teresinha Lopes CENDES et al. 2018. Toxic effects of phytol and retinol on human glioblastoma cells are associated with modulation of cholesterol and fatty acid biosynthetic pathways. Journal of neuro-oncology. 136, 435-443.
  54. Health Sciences Medicine (miscellaneous)
    Gambardella ANTONIO; Labate ANGELO; Mumoli LAURA; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2018. Role of pharmacogenomics in antiepileptic drug therapy: current status and future perspectives. Current pharmaceutical design. 23, 5760-5765.
  55. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Fernandes JANSEN; Andre Schwambach VIEIRA; Kramer Soares Juliana CARLOTA; Da Silva Eduardo ALVES; Lee Kil SUN et al. 2018. Hippocampal microrna-mrna regulatory network is affected by physical exercise. Biochimica et biophysica acta-general subjects. e, e-.
  56. Life Sciences Neuroscience (miscellaneous)
    Faber INGRID; Martinez Alberto Rolim MURO; De Rezende Thiago JUNQUEIRA; Júnior Carlos Roberto MARTINS; Martins Melina PAZIAN et al. 2018. Spg11 mutations cause widespread white matter and basal ganglia abnormalities; but restricted cortical damage. Neuroimage-clinical. 9, 848-857.
  57. Life Sciences Genetics
    De Andrade Helen Maia TAVARES; Cintra Vívian PEDIGONE; De Albuquerque MILENA; Piccinin Camila CALLEGARI; Bonadia Luciana CARDOSO et al. 2018. Intermediate-length cag repeat in atxn2 is associated with increased risk for amyotrophic lateral sclerosis in brazilian patients. Neurobiology of aging. 18, 30154-30154.
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    Vieira A S; Dogini D B; Iscia Teresinha Lopes CENDES. 2018. Role of non-coding rnas in non-aging-related neurological disorders. Brazilian journal of medical and biological research (on line). 51, e7566-.
  59. Life Sciences Neurology
    Alhusaini SAUD; Kowalczyk Magdalena A; Yasuda Clarissa L; Semmelroch Mira K; Katsurayama MARILISE et al. 2018. Normal cerebral cortical thickness in first-degree relatives of temporal lobe epilepsy patients. Neurology. 1, 10.1212/WNL.0000000000006834-.
  60. Life Sciences Neuroscience (miscellaneous)
    Rezende Thiago Junqueira RIBEIRO; De Paiva Jean Levi RIBEIRO; Martinez Alberto Rolim MURO; Iscia Teresinha Lopes CENDES; Pedroso José LUIZ et al. 2018. Structural signature of sca3: from presymptomatic to late disease stages. Annals of neurology. 84, 401-408.
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    Damasceno SAMARA; Menezes Nathália Bustamante DE; Rocha Cristiane De SOUZA; Matos Alexandre Hilário Berenguer DE; Andre Schwambach VIEIRA et al. 2018. Transcriptome of the wistar audiogenic rat (war) strain following audiogenic seizures. Epilepsy research. 147, 22-.
  62. Health Sciences Medicine (miscellaneous)
    Mota Marcelo Vilas BOAS; Zaidan Bruna CUNHA; Do Canto Amanda MORATO; Ghizoni ENRICO; Tedeschi HELDER et al. 2018. Atp synthase subunit beta immunostaining is reduced in the sclerotic hippocampus of epilepsy patients. Cellular and molecular neurobiology. 1, epub-.
  63. Life Sciences Neurology
    Rezende Thiago Junqueira R; Martinez Alberto Rolim M; Faber INGRID; Girotto KAREN; Martins Melina P et al. 2018. Developmental and neurodegenerative damage in friedreich ataxia. European journal of neurology. 1, epub-.
  64. Life Sciences Genetics
    Martins Junior Carlos ROBERTO; Borba Fabrício Castro DE; Martinez Alberto Rolim MURO; Rezende Thiago Junqueira Ribeiro DE; Iscia Teresinha Lopes CENDES et al. 2018. Twenty-five years since the identification of the first sca gene: history; clinical features and perspectives for sca1. Arquivos de neuro-psiquiatria (online). 76, 555-562.
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    Takazaki Karen A G; Rezende Thiago Junqueira R; Martinez Alberto R M; Gonzalez Salazar CARELIS; Nucci ANAMARLI et al. 2018. Sudomotor dysfunction is frequent and correlates with disability in friedreich ataxia. Clinical neurophysiology. 129, 2290-2295.
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    Contessotto Miriam G G; Rosselli Murai Luciana K; Garcia Maria Cristina C; Oliveira Cristiano L P; Torriani Iris L et al. 2018. The machado-joseph disease-associated expanded form of ataxin-3: overexpression; purification; and preliminary biophysical and structural characterization. Protein expression and purification. 152, 40-45.
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    Faber INGRID; Martinez Alberto Rolim MURO; Martins Carlos ROBERTO; Maia Maidane LUISE; Souza Juliana PASQUOTTO et al. 2018. Spg11-related parkinsonism: clinical profile; molecular imaging and <scp>l</scp> -dopa response. Movement disorders. 33, 1650-1656.
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    De Souza WÉLLITON; Carvalho Benilton De SÁ; Iscia Teresinha Lopes CENDES. 2018. Rqc</b> : a bioconductor</b> package for quality control of high-throughput sequencing data. Journal of statistical software. 87, 1-.
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    Ingrid FABER; Prota J R M; A R M MARTINEZ; Iscia Teresinha Lopes CENDES; França M C. 2017. A new phenotype associated with homozygous mutations: complicated spastic paraplegia. European journal of neurology (print). 24, e3-e4.
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    Silva Alves Mariana S; Secolin RODRIGO; Carvalho Benilton S; Yasuda Clarissa L; Bilevicius ELIZABETH et al. 2017. A prediction algorithm for drug response in patients with mesial temporal lobe epilepsy based on clinical and genetic information. Plos one. 12, e0169214-.
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    Martinez Alberto R M; Moro ADRIANA; Abrahao AGESSANDRO; Faber INGRID; Borges Conrado R et al. 2017. Nonneurological involvement in late-onset friedreich ataxia (lofa): exploring the phenotypes. Cerebellum (london. print). 16, 253-256.
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    Barros Fontes Marshall I; Dos Santos Ana P; Rossi Torres FÁBIO; Iscia Teresinha Lopes CENDES; Fernando CENDES et al. 2017. 17p13.3 microdeletion: insights on genotype-phenotype correlation. Molecular syndromology. 8, 36-41.
  73. Health Sciences Neurology (clinical)
    Avansini Simoni H; De Sousa Lima Beatriz PEREIRA; Secolin RODRIGO; Santos Marilza L; Coan Ana CAROLINA et al. 2017. Microrna hsa-mir-134 is a circulating biomarker for mesial temporal lobe epilepsy. Plos one. 12, e0173060-.
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    Rezende Thiago Junqueira R; Martinez Alberto Rolim M; Faber INGRID; Girotto KAREN; Pedroso José LUIZ et al. 2017. Structural signature of classical versus late-onset friedreich's ataxia by multimodality brain mri. Human brain mapping. 38, 4157-4168.
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    Vilany LARISSA; De Rezende Thiago J R; Piovesana Luiza G; Campos Lidiane S; De Azevedo Paula C et al. 2017. Exploratory structural assessment in craniocervical dystonia: global and differential analyses. Plos one. 12, e0182735-.
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    Rabelo Ana GB; Teixeira Camila VL; Magalhães Thamires NC; Carletti Cassani Ana Flávia MK; Amato Filho Augusto CS et al. 2017. Is cerebral microbleed prevalence relevant as a biomarker in amnestic mild cognitive impairment and mild alzheimer?s disease?. The neuroradiology journal. 30, 477-485.
  77. Life Sciences Biochemistry
    Silva Vinícius R; Secolin RODRIGO; Vemuganti RAGHU; Iscia Teresinha Lopes CENDES; Hazell Alan S. 2017. Acute liver failure is associated with altered cerebral expression profiles of long non-coding rnas. Neuroscience letters. 656, 58-64.
  78. Life Sciences Neuroscience (miscellaneous)
    Amorim Rebeca PADRÃO; Araújo Michelle Gasparetti LEÃO; Valero JORGE; Iscia Teresinha Lopes CENDES; Pascoal Vinicius Davila BITENCOURT et al. 2017. Silencing of p2x7r by rna interference in the hippocampus can attenuate morphological and behavioral impact of pilocarpine-induced epilepsy. Purinergic signalling. 1, 1-12.
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    Mccormack MARK; Gui HONGSHENG; Ingason ANDRÉS; Speed DOUG; Wright Galen E B et al. 2017. Genetic variation in cfh</i> predicts phenytoin-induced maculopapular exanthema in european-descent patients. Neurology. 90, 10.1212/WNL.00-.
  80. Health Sciences Medicine (miscellaneous)
    Ferreira Leslie ECKER; França Paulo Henrique Condeixa DE; Nagel VIVIAN; Venancio VANESSA; Safanelli JULIANA et al. 2017. Joinville stroke biobank: study protocol and first year?s results. Arquivos de neuro-psiquiatria. 75, 881-889.
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    De Azevedo Paula C; Guimarães Rachel P; Piccinin Camila C; Piovesana Luiza G; Campos Lidiane S et al. 2017. Cerebellar gray matter alterations in huntington disease: a voxel-based morphometry study. Cerebellum. 16, 923-928.
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    Martins Carlos ROBERTO; Martinez Alberto Rolim MURO; De Rezende Thiago Junqueira RIBEIRO; Branco Lucas Melo TEIXEIRA; Pedroso José LUIZ et al. 2017. Spinal cord damage in spinocerebellar ataxia type 1. Cerebellum. 16, 792-796.
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    Quaresma P G F; Weissmann L; Zanotto T M; Santos A C; De Matos A H B et al. 2017. Cdc2-like kinase 2 in the hypothalamus is necessary to maintain energy homeostasis. International journal of obesity. 41, 268-278.
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    Faber Ingrid VASCONCELLOS; Prota Joana Rosa MARQUES; Martinez Alberto Rolim MURO; Nucci ANAMARLI; Iscia Teresinha Lopes CENDES et al. 2017. Inflammatory demyelinating neuropathy heralding accelerated chediak-higashi syndrome. Muscle & nerve. 55, 756-760.
  85. Health Sciences Medicine (miscellaneous)
    K R SERVELHERE; Ingrid FABER; J A M SAUTE; Moscovich M; Anelyssa D ABREU et al. 2016. Non-motor symptoms in patients with hereditary spastic paraplegia caused by spg4 mutations. European journal of neurology (print). 23, 408-411.
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    André Schwambach VIEIRA; De Matos A H; Do Canto A M; Cristiane De Souza ROCHA; Benilton De Sá CARVALHO et al. 2016. Rna sequencing reveals region-specific molecular mechanisms associated with epileptogenesis in a model of classical hippocampal sclerosis. Scientific reports. 6, 22416-.
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    De Andrade Helen M T; De Albuquerque MILENA; Avansini Simoni H; De S Rocha CRISTIANE; Dogini Danyella B et al. 2016. Micrornas-424 and 206 are potential prognostic markers in spinal onset amyotrophic lateral sclerosis. Journal of the neurological sciences. 368, 19-24.
  88. Health Sciences Immunology and Allergy
    Ignarro Raffaela SILVESTRE; Facchini GUSTAVO; Vieira André SCHWAMBACH; De Melo Daniela RODRIGUES; Iscia Teresinha Lopes CENDES et al. 2016. Sulfasalazine intensifies temozolomide cytotoxicity in human glioblastoma cells. Molecular and cellular biochemistry. 418, 167-178.
  89. Health Sciences Neurology (clinical)
    Martinez Alberto R M; Nunes Marcelo B; Faber INGRID; D Abreu ANELYSSA; Iscia Teresinha Lopes CENDES et al. 2016. Fatigue and its associated factors in spinocerebellar ataxia type 3/machado-joseph disease. Cerebellum (london. print). 1, na-.
  90. Life Sciences Neuroscience (miscellaneous)
    Barbalho Patrícia GONÇALVES; Iscia Teresinha Lopes CENDES; Maurer Morelli Claudia VIANNA. 2016. Indomethacin treatment prior to pentylenetetrazole-induced seizures downregulates the expression of il1b and cox2 and decreases seizure-like behavior in zebrafish larvae. Bmc neuroscience (online). 17, 12-.
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    Barbalho Patrícia GONÇALVES; Carvalho Benilton De SÁ; Iscia Teresinha Lopes CENDES; Maurer Morelli Claudia VIANNA. 2016. Cyclooxygenase-1 as a potential therapeutic target for seizure suppression: evidences from zebrafish pentylenetetrazole-seizure model. Frontiers in neurology. 7, 200-.
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    Lopes Ramos C M; Pereira T C; Dogini D B; Gilioli R; Iscia Teresinha Lopes CENDES. 2016. Lithium carbonate and coenzyme q10 reduce cell death in a cell model of machado-joseph disease. Brazilian journal of medical and biological research. 49, e5805-.
  93. Life Sciences Genetics
    Piovesana L G; F R TORRES; Azevedo P C; Amaral T P; Iscia Teresinha Lopes CENDES et al. 2016. New thap1</i> mutation and role of putative modifier in tor1a</i>. Acta neurologica scandinavica. 135, n/a-n/a.
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    Silva Luiz Fernando De Almeida Lima E; Loureiro Júlia CUNHA; Franco Stephany Caroline RAPOSO; Santos Marilza De LIMA; Secolin RODRIGO et al. 2016. Assessing treatment response to prophylactic lithium use in patients with bipolar disorder. Jornal brasileiro de psiquiatria. 65, 9-16.
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    De Rezende T J R; D Abreu A; Guimarães R P; Lopes T M; Iscia Teresinha Lopes CENDES et al. 2015. Cerebral cortex involvement in machado−joseph disease. European journal of neurology (print). 22, 277-283.
  96. Life Sciences Neuroscience (miscellaneous)
    Piccinin Camila C; Piovesana Luiza G; Santos Maria C A; Guimarã Es Rachel P; De Campos Brunno M et al. 2015. Diffuse decreased gray matter in patients with idiopathic craniocervical dystonia: a voxel-based morphometry study. Frontiers in neurology. 5, 283-283.
  97. Health Sciences Medicine (miscellaneous)
    Rezende Thiago J R; De Albuquerque MILENA; Lamas Gustavo M; Martinez Alberto R M; Campos Brunno M et al. 2015. Multimodal mri-based study in patients with spg4 mutations. Plos one. 10, e0117666-.
  98. Health Sciences Neurology (clinical)
    Martins Carlos R; Martinez Alberto R M; D Abreu ANELYSSA; Iscia Teresinha Lopes CENDES; França Marcondes C. 2015. Fatigue is frequent and severe in spinocerebellar ataxia type 1. Parkinsonism & related disorders. 21, 821-822.
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    Giordanna PINHEIRO; Rachel Paes GUIMARÃES; Luiza PIOVESANA; Brunno CAMPOS; Lidiane CAMPOS et al. 2015. White matter microstructure in idiopathic craniocervical dystonia. Tremor and other hyperkinetic movements. 28, 5-302-.
  100. Life Sciences Neurology
    Gonsales Marina C; Montenegro Maria AUGUSTA; Soler Camila V; Coan Ana CAROLINA; Guerreiro Marilisa M et al. 2015. Recent developments in the genetics of childhood epileptic encephalopathies: impact in clinical practice. Arquivos de neuro-psiquiatria (online). 73, 946-958.
  101. Health Sciences Neurology (clinical)
    Nunes Marcelo B; Martinez Alberto Rolim M; Rezende Thiago Junqueira R; Friedman Joseph H; Iscia Teresinha Lopes CENDES et al. 2015. Dystonia in machado-joseph disease: clinical profile; therapy and anatomical basis. Parkinsonism & related disorders. 21, 1441-1447.
  102. Health Sciences Nutrition and Dietetics
    Quaresma P G F; Reencober N; Zanotto T M; Santos A C; Weissmann L et al. 2015. Pioglitazone treatment increases food intake and decreases energy expenditure partially via hypothalamic adiponectin/adipor1/ampk pathway. International journal of obesity. 40, 138-146.
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    Rezende Thiago J R; Silva Cynthia B; Yassuda Clarissa L; Campos Brunno M; D Abreu ANELYSSA et al. 2015. Longitudinal magnetic resonance imaging study shows progressive pyramidal and callosal damage in friedreich's ataxia. Movement disorders. 1, n/a-n/a.
  104. Health Sciences Neurology (clinical)
    Simões Priscila Santos RODRIGUES; Visniauskas BRUNA; Perosa Sandra REGINA; Elza Márcia Targas YACUBIAN; Centeno RICARDO et al. 2014. Expression and activity of thimet oligopeptidase (top) are modified in the hippocampus of subjects with temporal lobe epilepsy (tle). Epilepsia (copenhagen). 55, 754-762.
  105. Health Sciences Medicine (miscellaneous)
    Bonilha Da Silva C; Felipe P G BERGO; D Abreu A; Fernando CENDES; Iscia Teresinha Lopes CENDES et al. 2014. Dentate nuclei t2 relaxometry is a reliable neuroimaging marker in friedreich's ataxia. European journal of neurology (print). 21, 1131-1136.
  106. Life Sciences Neuroscience (miscellaneous)
    Suemitsu Luciana Akemi YASUDA; Clarissa Lin YASUDA; Morita Marcia ELISABETE; Beltramini Guilherme COCO; Coan Ana CAROLINA et al. 2014. Longitudinal analysis of hippocampal t2 relaxometry in fmtle. Epilepsy & behavior (print). 36, 154-158.
  107. Life Sciences Endocrinology
    Lais WEISSMANN; Quaresma P G F; Andressa C SANTOS; De Matos A H B; Vinicius D Avila Bitencourt PASCOAL et al. 2014. Ikk epsilon is key to induction of insulin resistance in the hypothalamus and its inhibition reverses obesity. Diabetes (new york; n.y.). 8, 1797-.
  108. Life Sciences Genetics
    França M C; Dogini D B; D Abreu A; Helio Afonso Ghizoni TEIVE; Munhoz R P et al. 2014. Spg4-related hereditary spastic paraplegia: frequency and mutation spectrum in brazil. Clinical genetics. 86, 194-196.
  109. Life Sciences Endocrinology
    Morari J; Anhe G F; Nascimento L F; De Moura R F; Razolli D et al. 2014. Fractalkine (cx3cl1) is involved in the early activation of hypothalamic inflammation in experimental obesity. Diabetes (new york; n.y.). 63, 3770-3784.
  110. Life Sciences Neurology
    Fahl Camila N; Branco Lucas Melo T; Felipe Paulo Guazzi BERGO; D Abreu ANELYSSA; Iscia Teresinha Lopes CENDES et al. 2014. Spinal cord damage in machado-joseph disease. Cerebellum (london. print). xx, xx-xx.
  111. Health Sciences Neurology (clinical)
    Ingrid FABER; K R SERVELHERE; A R M MARTINEZ; Anelyssa Cysne Frota D ABREU; Iscia Teresinha Lopes CENDES et al. 2014. Clinical features and management of hereditary spastic paraplegia. Arquivos de neuro-psiquiatria. 72, 219-226.
  112. Health Sciences Neurology (clinical)
    Piccinin Camila C; Santos Maria C A; Piovesana Luiza G; Campos Lidiane S; Guimarães Rachel P et al. 2014. Infratentorial gray matter atrophy and excess in primary craniocervical dystonia. Parkinsonism & related disorders. 20, 198-203.
  113. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Danyella Barbosa DOGINI; Pascoal Vinícius D Avila BITTENCOURT; Avansini Simoni HELENA; Vieira André SCHWAMBACH; Tiago Campos PEREIRA et al. 2014. The new world of rnas. Genetics and molecular biology. 37, 285-293.
  114. Health Sciences Neurology (clinical)
    Takazaki Karen A G; D Abreu ANELYSSA; Anamarli NUCCI; Iscia Teresinha Lopes CENDES; França Marcondes C. 2013. Dysautonomia is frequent in machado-joseph disease: clinical and neurophysiological evaluation. Cerebellum (london. print). 513-519.
  115. Health Sciences Psychiatry and Mental Health
    Rodrigo SECOLIN; Banzato Claudio E M; Mella Lucas F B; Santos Marilza L; Dalgalarrondo PAULO et al. 2013. Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder. American journal of medical genetics. part b; neuropsychiatric genetics. 162, 163-168.
  116. Health Sciences Medicine (miscellaneous)
    Tiago Campos PEREIRA; Cláudia Carolina S EVANGELISTA; Gustavo BORGES; Eliana M Zanotti MAGALHÃES; Luiz A MAGALHAES et al. 2013. Applications of rna interference in schistosomiasis: gene function identification and development of new therapies. Isrn parasitology. 2013, 1-10.
  117. Life Sciences Neurology
    Chevis Camila F; Silva Cynthia B; D Abreu ANELYSSA; Iscia Teresinha Lopes CENDES; Cendes FERNANDO et al. 2013. Spinal cord atrophy correlates with disability in friedreich¿s ataxia. Cerebellum (london. print). 12, 43-47.
  118. Health Sciences Genetics (clinical)
    Monteiro Fabíola P; Vieira Társis P; Sgardioli Ilária C; Molck Miriam C; Damiano Ana PAULA et al. 2013. Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature. European journal of pediatrics. 172, 927-945.
  119. Health Sciences Neurology (clinical)
    Guimarães Rachel P; D Abreu ANELYSSA; Yasuda Clarissa L; França Marcondes C; Silva Beatriz H B et al. 2013. A multimodal evaluation of microstructural white matter damage in spinocerebellar ataxia type 3. Movement disorders. 28, 1125-1132.
  120. Health Sciences Neurology (clinical)
    Pedroso José LUIZ; França Marcondes C; Braga Neto PEDRO; D Abreu ANELYSSA; Saraiva Pereira Maria LUIZA et al. 2013. Nonmotor and extracerebellar features in machado-joseph disease: a review. Movement disorders. 28, 1200-1208.
  121. Life Sciences Neurology
    Lopes Tátila MARTINS; D Abreu ANELYSSA; Junior Marcondes Cavalcante FRANÇA; Clarissa Lin YASUDA; Betting Luiz EDUARDO et al. 2013. Widespread neuronal damage and cognitive dysfunction in spinocerebellar ataxia type 3. Journal of neurology (print). 260, 2370-2379.
  122. Health Sciences Neurology (clinical)
    Casseb R F; D Abreu A; Ruocco H H; Iscia Teresinha Lopes CENDES; F CENDES et al. 2013. Thalamic metabolic abnormalities in patients with huntington's disease measured by magnetic resonance spectroscopy. Brazilian journal of medical and biological research on line. 46, 722-727.
  123. Health Sciences Neurology (clinical)
    Scorza Fulvio A; Fernando CENDES; Cavalheiro Esper A; Iscia Teresinha Lopes CENDES. 2013. Sudden unexpected death in epilepsy: small rnas raise expectations. Epilepsy & behavior (print). 29, 591-593.
  124. Health Sciences Immunology and Allergy
    Rabelo Gonçalves Elizabeth Maria AFONSO; Sgardioli Ilária C; Iscia Teresinha Lopes CENDES; Escanhoela Cecília Amélia FAZZIO; Almeida Jazon Romilson De SOUZA et al. 2013. Improved detection of helicobacter pylori</i> dna in formalin-fixed paraffin-embedded (ffpe) tissue of patients with hepatocellular carcinoma using laser capture microdissection (lcm). Helicobacter (cambridge; mass.). 18, 244-245.
  125. Life Sciences Neurology
    Danyella Barbosa DOGINI; Avansini Simoni H; Vieira Andre S; Iscia Teresinha Lopes CENDES. 2013. Microrna regulation and dysregulation in epilepsy. Frontiers in cellular neuroscience. 7, 1-8.
  126. Life Sciences Neuroscience (miscellaneous)
    Avansini Simoni HELENA; Torres Fábio ROSSI; Dogini Danyella B; Fábio ROGÉRIO; Coan Ana CAROLINA et al. 2013. Down-regulation of dicer1 leading to abnormal expression of mature micrornas and neurog2 is involved with aberrant neuroglial differentiation in focal cortical dysplasias (fcd) (s08.002). Neurology (cleveland; ohio). 12, 80-.
  127. Life Sciences Neurology
    Avansini Simoni HELENA; Torres Fábio ROSSI; Dogini Danyella B; Rogerio FABIO; Coan Ana CAROLINA et al. 2013. Evidence pointing to failure in neuroglial differentiation in focal cortical dysplasia (fcd) type ii. Epilepsia (copenhagen). 54, 293-.
  128. Life Sciences Neuroscience (miscellaneous)
    Da Silva Cynthia B; Chevis Camila F; D Abreu ANELYSSA; Iscia Teresinha Lopes CENDES; França Marcondes C. 2013. Fatigue is frequent and multifactorial in friedreich's ataxia. Parkinsonism & related disorders. 19, 766-7.
  129. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Tiago Campos PEREIRA; Iscia Teresinha Lopes CENDES. 2013. Medical applications of rna interference (rnai). Bmc proceedings. 7, K21-.
  130. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Maurer Morelli Claudia V; De Vasconcellos Jaira F; Reis Pinto Fernanda C; Rocha Cristiane De S; Domingues Romenia R et al. 2012. A comparison between different reference genes for expression studies in human hippocampal tissue. Journal of neuroscience methods. 208, 44-47.
  131. Life Sciences Genetics
    Teive HÉLIO; Renato P MUNHOZ; W O ARRUDA; Iscia Teresinha Lopes CENDES; Salmo RASKIN et al. 2012. Spinocerebellar ataxias ¿ genotype-phenotype correlations in 104 brazilian families. Clinics (usp. impresso). 67, 443-449.
  132. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Tiago Campos PEREIRA; Iscia Teresinha Lopes CENDES. 2012. Emerging rna-based drugs: sirnas; micrornas and derivates. Central nervous system agents in medicinal chemistry. 12, 217-232.
  133. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 2012. Do we need a new look in the definition of x-linked recessive disorders?. Arquivos de neuro-psiquiatria (impresso). 70, 483-484.
  134. Life Sciences Genetics
    Franca M C; Yasuda C L; Fabricio R S PEREIRA; D Apos Abreu A; Lopes Ramos C M et al. 2012. White and grey matter abnormalities in patients with spg11 mutations. Journal of neurology; neurosurgery and psychiatry. 83, 828-833.
  135. Health Sciences Medicine (miscellaneous)
    Maurer Morelli Cláudia V; Eliane KOBAYASHI; Neide F SANTOS; Iscia Teresinha Lopes CENDES; Domingues Romênia R et al. 2012. A locus identified on chromosome18p11.31 is associated with hippocampal abnormalities in a family with mesial temporal lobe epilepsy. Frontiers in neurology. 3, 1-7.
  136. Health Sciences Medicine (miscellaneous)
    M E MORITA; Yasuda C L; Luis E BETTING; Pacagnella D; L CONZ et al. 2012. Mri and eeg as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy. Neurology (online). 79, 2349-2354.
  137. Life Sciences Genetics
    Araújo Tânia KAWASAKI; Simioni MILENA; Félix Têmis MARIA; De Souza Liliane TODESCHINI; Fontes Marshall Ítalo BARROS et al. 2012. Preliminary analysis of the nonsynonymous polymorphism rs17563 in bmp4 gene in brazilian population suggests protection for nonsyndromic cleft lip and palate. Plastic surgery international (print). 2012, 1-5.
  138. Physical Sciences Artificial Intelligence
    Rodrigo SECOLIN; Pascoal Vinícius D Ávila BITENCOURT; Iscia Teresinha Lopes CENDES; Tiago Campos PEREIRA. 2012. Analysis of energetically biased transcripts of viruses and transposable elements. Genetics and molecular biology (impresso). 35, 868-873.
  139. Life Sciences Neuroscience (miscellaneous)
    Matos AHB; Pascoal VDB; Nascimento DR; Martins S; Rocha CS et al. 2012. A caracterização do perfil de expressão gênica em larga escala em modelos genéticos de epilepsia fornece elementos para entender os mecanismos envolvidos na epileptogênese em roedores. Journal of epilepsy and clinical neurophysiology (impresso). 18, 50-52.
  140. Life Sciences Genetics
    Gonsales MC; Preto P; Montenegro MA; Guerreiro MM; Iscia Teresinha Lopes CENDES. 2012. Correlações entre o genótipo e o fenótipo na síndrome de dravet com mutações em scn1a aumentam a acurácia do diagnóstico molecular. Journal of epilepsy and clinical neurophysiology (impresso). 18, 60-62.
  141. Health Sciences Neurology (clinical)
    Dogini Danyella B; Avansini Simoni HELENA; Fábio Rossi TORRES; Rogério FABIO; Rocha Cristiane S et al. 2012. Microrna expression profile in epilepsy: breaking molecular barriers. Journal of epilepsy and clinical neurophysiology (impresso). 18, 57-59.
  142. Life Sciences Genetics
    França Marcondes C; Emmel Vanessa E; Anelyssa Cysne Frota D ABREU; Maurer Morelli Cláudia V; Secolin RODRIGO et al. 2012. Normal atxn3 allele but not chip polymorphisms modulates age at onset in machado¿joseph disease. Frontiers in neurology. 3, 164-164.
  143. Life Sciences Neuroscience (miscellaneous)
    Silva Cynthia B; Yasuda Clarissa L; D Abreu ANELYSSA; Fernando CENDES; Iscia Teresinha Lopes CENDES et al. 2012. Neuroanatomical correlates of depression in friedreich?s ataxia: a voxel-based morphometry study. Cerebellum (london. print). 12, 429-436.
  144. Life Sciences Neurology
    Simioni MILENA; Vieira Társis PAIVA; Sgardioli Ilária CRISTINA; Freitas Érika LOPES; Rosenberg CARLA et al. 2012. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. American journal of medical genetics. part a. 11, 2905-2910.
  145. Health Sciences Medicine (miscellaneous)
    Paula Mimura PRETO; Guimarães Catarina A; Clarissa Lin YASUDA; Katia M R S SCHMUTZLER; Marina GONZALEZ et al. 2012. Clinical and eeg profile in dravet and doose syndromes. Journal of pediatric epilepsy. 1, 43-49.
  146. Health Sciences Medicine (miscellaneous)
    De Oliveira Márcia S; Anelyssa Cysne Frota D ABREU; França Jr Marcondes C; Iscia Teresinha Lopes CENDES; Fernando CENDES et al. 2012. Mri-texture analysis of corpus callosum; thalamus; putamen; and caudate in machado-joseph disease. Journal of neuroimaging. 22, 46-52.
  147. Health Sciences Pharmacology (medical)
    Siebert M; Donis K C; Socal M; Rieder C R M; Emmel V E et al. 2012. Glucocerebrosidase gene variants in parkinsonian patients with machado joseph/spinocerebellar ataxia 3. Parkinsonism & related disorders. 18, 185-190.
  148. Life Sciences Neurology
    Anelyssa Cysne Frota D ABREU; Anelyssa Cysne Frota D ABREU; Yasuda Clarissa L; Iscia Teresinha Lopes CENDES; Franã A Jr Marcondes C et al. 2011. Neocortical atrophy in machado-joseph disease: a longitudinal neuroimaging study. Journal of neuroimaging. 1, no-no.
  149. Health Sciences Radiology, Nuclear Medicine and Imaging
    Rachel Paes GUIMARÃES; Clarissa YASUDA; Anelyssa Cysne Frota D ABREU; Marcondes Franca JR; Iscia Teresinha Lopes CENDES et al. 2011. Diffusion tensor imaging (dti) and voxel based morphometry (vbm) analysis reveal white matter abnormalities in machado-joseph (mjd) disease. Neurology (cleveland; ohio). 76, A400-.
  150. Health Sciences Neurology (clinical)
    Fernando CENDES; Frederick ANDERMANN; F DUBEAU; P GLOOR; A EVANS et al. 2011. Early childhood prolonged febrile convulsions; atrophy and sclerosis of mesial structures; and temporal lobe epilepsy: an mri volumetric study. Neurology (cleveland; ohio). 76, 1845-1845.
  151. Health Sciences Neurology (clinical)
    Conz LIVIA; Morita Marcia ELISABETE; Ana Carolina COAN; Kobayashi ELIANE; Clarissa Lin YASUDA et al. 2011. Longitudinal mri volumetric evaluation in patients with familial mesial temporal lobe epilepsy. Frontiers in neurology. 2, 2-5.
  152. Health Sciences Neurology (clinical)
    D Abreu ANELYSSA; França Jr Macondes C; Yasuda Clarissa L; Souza Mariana S A; Iscia Teresinha Lopes CENDES et al. 2011. Thalamic volume and dystonia in machado-joseph disease. Journal of neuroimaging. 21, e91-e93.
  153. Life Sciences Pharmacology
    Iscia Teresinha Lopes CENDES; Guerreiro Carlos A M. 2011. Pharmacogenetics: reality or fiction? or are we there yet?. Arquivos de neuro-psiquiatria (impresso). 69, 151-152.
  154. Life Sciences Genetics
    Rodrigues Guilherme RICCIOPPO; Walker Ruth H; Bader BENEDIKT; Danek ADRIAN; Brice ALEXIS et al. 2011. Clinical and genetic analysis of 29 brazilian patients with huntington's disease-like phenotype. Arquivos de neuro-psiquiatria (impresso). 69, 419-423.
  155. Health Sciences Medicine (miscellaneous)
    Susana Barreto MORY; Betting Luiz E; Fernandes Paula T; Iscia Teresinha Lopes CENDES; Guerreiro Marilisa M et al. 2011. Structural abnormalities of the thalamus in juvenile myoclonic epilepsy. Epilepsy & behavior (print). 21, 407-411.
  156. Health Sciences Neurology (clinical)
    D Amp Apos Abreu ANELYSSA; França Jr Marcondes C; Paulson Henry L; Iscia Teresinha Lopes CENDES. 2010. Caring for machado¿joseph disease: current understanding and how to help patients?. Parkinsonism & related disorders. 16, 2-7.
  157. Life Sciences Neuroscience (miscellaneous)
    Rodrigo SECOLIN; Maurer Morelli CLAUDIA; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2010. Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy. Epilepsia (copenhagen). 51, 47-50.
  158. Health Sciences Neurology (clinical)
    Betting Luiz E; Li Li M; Iscia Teresinha Lopes CENDES; Guerreiro Marilisa M; Guerreiro Carlos A M et al. 2010. Correlation between quantitative eeg and mri in idiopathic generalized epilepsy. Human brain mapping (print). 31, 1327-1338.
  159. Health Sciences Neurology (clinical)
    Franã A Jr M C; Dâ Abreu A; A NUCCI; Iscia Teresinha Lopes CENDES. 2010. Clinical correlates of autonomic dysfunction in patients with machado-joseph disease. Acta neurologica scandinavica. 121, 422-425.
  160. Health Sciences Medicine (miscellaneous)
    Ottman RUTH; Hirose SHINICHI; Jain SATISH; Lerche HOLGER; Iscia Teresinha Lopes CENDES et al. 2010. Genetic testing in the epilepsies-report of the ilae genetics commission. Epilepsia (copenhagen). 51, 655-670.
  161. Health Sciences Physiology (medical)
    C L YASUDA; M E MORITA; Alessio A; A R PEREIRA; Balthazar M L F et al. 2010. Relationship between environmental factors and gray matter atrophy in refractory mtle. Neurology (cleveland; ohio). 74, 1062-1068.
  162. Life Sciences Clinical Biochemistry
    Reis Leonardo OLIVEIRA; Tiago Campos PEREIRA; Iscia Teresinha Lopes CENDES; Ferreira UBIRAJARA. 2010. Micrornas: a new paradigm on molecular urological oncology. Urology (ridgewood; n.j.). 76, 521-527.
  163. Health Sciences Medicine (miscellaneous)
    Simioni M; Freitas É LOPES; Vieira T PAIVA; Iscia Teresinha Lopes CENDES; Gil Da Silva Lopes V LÚCIA. 2010. Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism. Journal of applied genetics. 51, 219-221.
  164. Life Sciences Neurology
    Rodrigo SECOLIN; Banzato Cláudio E M; Oliveira Maria C M; Bittar Maria F R; Santos Marilza L et al. 2010. Family-based association study for bipolar affective disorder. Psychiatric genetics. 1-4.
  165. Life Sciences Neuroscience (miscellaneous)
    E BILEVICIUS; C L YASUDA; M S SILVA; C A M GUERREIRO; Iscia Teresinha Lopes CENDES et al. 2010. Antiepileptic drug response in temporal lobe epilepsy: a clinical and mri morphometry study. Neurology (cleveland; ohio). 75, 1695-1701.
  166. Life Sciences Neuroscience (miscellaneous)
    Vinicius D Ávila Bittencourt PASCOAL; Rafael B MARCHESINI; Alexandre Hilário Berenguer MATOS; Fábio Frangiotti CONTE; Tiago Campos PEREIRA et al. 2010. The il 1 β have a protective action in the acute phase of the pilocarpine-induced epilepsy model | [a interleucina 1-beta mostra uma ação protetora na fase aguda do modelo de epilepsia induzido pela pilocarpina]. Journal of epilepsy and clinical neurophysiology (impresso). 16, 97-99.
  167. Life Sciences Genetics
    Pedrazzoli MARIO; Rodrigo SECOLIN; Esteves Luiz Otávio BASTOS; Pereira Danyella SILVA; Koike Bruna Del VECHIO et al. 2010. Interactions of polymorphisms in different clock genes associated with circadian phenotypes in humans. Genetics and molecular biology (impresso). 627-632.
  168. Life Sciences Cancer Research
    Reis Leonardo OLIVEIRA; Tiago Campos PEREIRA; Favaro Wagner JOSÉ; Cagnon Valéria Helena ALVES; Iscia Teresinha Lopes CENDES et al. 2009. Experimental animal model and rna interference: a promising association for bladder cancer research. World journal of urology. 1-9.
  169. Health Sciences Medicine (miscellaneous)
    D Abreu A; França Jr M; L CONZ; Joseph H FRIEDMAN; Nucci A M et al. 2009. Sleep symptoms and their clinical correlates in machado-joseph disease. Acta neurologica scandinavica. 119, 277-280.
  170. Life Sciences Neuroscience (miscellaneous)
    D Amp Apos Abreu ANELYSSA; França Jr MARCONDES; Simone APPENZELLER; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2009. Axonal dysfunction in the deep white matter in machado-joseph disease. Journal of neuroimaging. 19, 9-12.
  171. Health Sciences Neurology (clinical)
    França Marcondes C; D Abreu ANELYSSA; Yasuda Clarissa L; Bonadia Luciana CARDOSO; Santos Da Silva MARILZA et al. 2009. A combined voxel-based morphometry and 1h-mrs study in patients with friedreich¿s ataxia. Journal of neurology. 256, 1114-1120.
  172. Life Sciences Cell Biology
    Pereira T C; Iscia Teresinha Lopes CENDES. 2009. Cryptic anhydrobiotic potential in man: implications in medicine. Medical hypotheses. 73, 506-507.
  173. Health Sciences Neurology (clinical)
    França Marcondes C; Anelyssa Cysne Frota D ABREU; Anamarli NUCCI; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2009. Progression of ataxia in patients with machado-joseph disease. Movement disorders. 24, 1387-1390.
  174. Health Sciences Neurology (clinical)
    C Fran A MARCONDES; D Amp Apos Abreu ANELYSSA; Anamarli NUCCI; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2009. Prospective study of peripheral neuropathy in machado???joseph disease. Muscle & nerve (print). 40, 1012-1018.
  175. Life Sciences Neuroscience (miscellaneous)
    Conte Fábio F; Ribeiro Patrícia A O; Marchesini Rafael B; Pascoal Vinícius D B; Silva Joelcimar M et al. 2009. Expression profile and distribution of efhc1 gene transcript during rodent brain development. Journal of molecular neuroscience. 39, 69-77.
  176. Life Sciences Behavioral Neuroscience
    Pereira Ana Helena M; Clemente Carolina F M Z; Cardoso Alisson C; Theizen Thais H; Rocco Silvana A et al. 2009. Mef2c silencing attenuates load-induced left ventricular hypertrophy by modulating mtor/s6k pathway in mice. Plos one. 4, e8472-.
  177. Life Sciences Neurology
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Clarissa Lin YASUDA; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2008. Correlação entre sintomas motores e grau de atrofia cerebral e cerebelar em pacientes com doença de machado-joseph. Arquivos de neuro-psiquiatria. 66, 229-229.
  178. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2008. A genética das epilepsias. Jornal de pediatria. 84, S33-S39.
  179. Life Sciences Neuroscience (miscellaneous)
    Ruocco H H; Bonilha L; L M LI; Iscia Teresinha Lopes CENDES; F CENDES. 2008. Longitudinal analysis of regional grey matter loss in huntington disease: effects of the length of the expanded cag repeat. Journal of neurology; neurosurgery and psychiatry. 79, 130-135.
  180. Health Sciences Neurology (clinical)
    Oliveira E; Hage S; Guimaraes C; Brandaoalmeida I; Iscia Teresinha Lopes CENDES et al. 2008. Characterization of language and reading skills in familial polymicrogyria. Brain & development (tokyo). 30, 254-260.
  181. Life Sciences Genetics
    Viana Danilo V; Góes Juvenal R N; Coy Cláudio S R; Lourdes Setsuko Ayrizono MARIA; Lima Carmen S P et al. 2008. Family history of cancer in brazil: is it being used?. Familial cancer. 7, 229-232.
  182. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Pereira T; Iscia Teresinha Lopes CENDES. 2008. Rnai-mediated gene silencing as a principle of action of venoms and poisons. Medical hypotheses. 70, 1179-1181.
  183. Life Sciences Genetics
    Pereira T; Pascoal V; Marchesini R; Maia I; Magalhaes L et al. 2008. Schistosoma mansoni: evaluation of an rnai-based treatment targeting hgprtase gene. Experimental parasitology. 118, 619-623.
  184. Life Sciences Genetics
    Neide F SANTOS; Rodrigo SECOLIN; Brandão Almeida Iara L; Silva Marilza S; Torres Fábio R et al. 2008. A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome xq27. American journal of medical genetics. 146A, 1151-1157.
  185. Health Sciences Radiology, Nuclear Medicine and Imaging
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Veronica A ZANARDI; A V FARIA; Iscia Teresinha Lopes CENDES et al. 2008. Mri shows dorsal lesions and spinal cord atrophy in chronic sensory neuronopathies. Journal of neuroimaging. 1, 168-172.
  186. Physical Sciences Artificial Intelligence
    R SECOLIN; Rocha C; Torres F; Santos M; Maurermorelli C et al. 2008. Linkgen: a new algorithm to process data in genetic linkage studies. Genomics (san diego). 91, 544-547.
  187. Life Sciences Neuroscience (miscellaneous)
    Tsuneda Simone S; Torres Fabio R; Montenegro Maria A; Guerreiro Marilisa M; Fernando CENDES et al. 2008. A new missense mutation found in the flna gene in a family with bilateral periventricular nodular heterotopia (bpnh) alters the splicing process. Journal of molecular neuroscience. 35, 195-200.
  188. Health Sciences Medicine (miscellaneous)
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Anamarli NUCCI; Iscia Teresinha Lopes CENDES. 2008. Muscle excitability abnormalities in machado-joseph disease. Archives of neurology (chicago). 65, 525-529.
  189. Life Sciences Neuroscience (miscellaneous)
    Ribeiro Patrícia A O; Lourenço SBRAGIA; Rovilson GILIOLI; Langone FRANCESCO; Conte Fábio F et al. 2008. Expression profile of lgi1 gene in mouse brain during development. Journal of molecular neuroscience. 1-4.
  190. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Tiago Campos PEREIRA; Iscia Teresinha Lopes CENDES. 2008. Central in novel nucleic acid-based agents: sirnas and mirnas. Central nervous system agents in medicinal chemistry. 8, 121-130.
  191. Health Sciences Medicine (miscellaneous)
    Murai M; Sassonia R; Zamboni A; Conte F; Martinsdesouza D et al. 2008. Characterization of the c-terminal half of human juvenile myoclonic epilepsy protein efhc1: dimer formation blocks ca2+ and mg2+ binding to its functional ef-hand. Archives of biochemistry and biophysics. 1-.
  192. Life Sciences Microbiology
    Talita M MARIN; Clemente C F M Z; Aline M SANTOS; Paty K PICARDI; Pascoal V D B et al. 2008. Shp2 negatively regulates growth in cardiomyocytes by controlling focal adhesion kinase/src and mtor pathways. Circulation research. 103, 813-824.
  193. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Dogini Danyella B; Ribeiro Patrícia A O; Cristiane ROCHA; Pereira Tiago C; Iscia Teresinha Lopes CENDES. 2008. Microrna expression profile in murine central nervous system development. Journal of molecular neuroscience. 35, 331-337.
  194. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2008. The genetics of epilepsies. Jornal de pediatria. 0, 33-39.
  195. Health Sciences Neurology (clinical)
    Brandão Almeida I; Simone HAGE; E OLIVEIRA; Guimarães C; Teixeira K et al. 2008. Congenital bilateral perisylvian syndrome: familial occurrence; clinical and psycholinguistic aspects correlated with mri. Neuropediatrics. 39, 139-145.
  196. Health Sciences Medicine (miscellaneous)
    Fábio Rossi TORRES; Souza Kols Daniela Aguiar DE; Simone Sayuri TSUNEDA; Rodrigo SECOLIN; Iara Leda Brandão De ALMEIDA et al. 2008. Estudos genéticos e moleculares em um grande grupo de pacientes com malformações do córtex cerebral. Journal of epilepsy and clinical neurophysiology (impresso). 14, 101-105.
  197. Health Sciences Neurology (clinical)
    Morita Márcia E; Conz LÍVIA; Maurer Morelli Claudia V; Eliane KOBAYASHI; Yasuda Clarissa L et al. 2008. Long term follow up of familial mesial temporal lobe epilepsy. Journal of epilepsy and clinical neurophysiology (impresso). 14, 111-113.
  198. Life Sciences Neuroscience (miscellaneous)
    Maurer Morelli Cláudia VIANNA; Marchesini Rafael BREGLIO; Rodrigo SECOLIN; Santos Neide FERREIRA; Eliane KOBAYASHI et al. 2007. Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy. Arquivos de neuro-psiquiatria. 65, (1) 20-23.
  199. Health Sciences Neurology (clinical)
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Joseph H FRIEDMAN; Anamarli NUCCI; Iscia Teresinha Lopes CENDES. 2007. Chronic pain in machado-joseph disease: a frequent and disabling symptom. Archives of neurology (chicago). 64, 1767-1770.
  200. Health Sciences Neurology (clinical)
    Ruocco Heloísa H; Iscia Teresinha Lopes CENDES; Li Li M; Fernando CENDES. 2007. Evidence of thalamic dysfunction in huntington disease by proton magnetic resonance spectroscopy. Movement disorders. 22, 2052-2056.
  201. Life Sciences Neurology
    D Amp Apos Abreu ANELYSSA; Franca MARCONDES; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2007. The international cooperative ataxia rating scale in machado-joseph disease. comparison with the unified multiple system atrophy rating scale. Movement disorders. 22, 1976-1979.
  202. Health Sciences Neurology (clinical)
    Montenegro Maria AUGUSTA; Fernando CENDES; Iscia Teresinha Lopes CENDES; Guerreiro Carlos A M; Li Li M et al. 2007. The clinical spectrum of malformations of cortical development. Arquivos de neuro-psiquiatria. 65, 196-201.
  203. Health Sciences Neurology (clinical)
    França Marcondes C; D Amp Apos Abreu ANELYSSA; Maurer Morelli Cláudia V; Seccolin RODRIGO; Simone APPENZELLER et al. 2007. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum. Movement disorders. 22, 1556-1562.
  204. Life Sciences Molecular Biology
    Clemente C F M Z; T F TORNATORE; T H THEIZEN; A C DECKMANN; Pereira T C et al. 2007. Targeting focal adhesion kinase with small interfering rna prevents and reverses load-induced cardiac hypertrophy in mice. Circulation research. 101, 1339-1348.
  205. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Tiago Campos PEREIRA; Bittencourt Vinícius D Amp Apos Ávila PASCOAL; Rodrigo SECOLIN; Rocha Cristiane De SOUZA; Maia Ivan De GODOY et al. 2007. Strand analysis; a free online program for the computational identification of the best rna interference (rnai) targets based on gibbs free energy. Genetics and molecular biology. 30, 1206-1208.
  206. Life Sciences Neuroscience (miscellaneous)
    Maria Augusta MONTENEGRO; Demet KINAT; Fernando CENDES; Andrea BERNASCONI; A C COAN et al. 2006. Patterns of hippocampal abnormalities in malformations of cortical development. Journal of neurology; neurosurgery and psychiatry. 77, (3) 367-371.
  207. Life Sciences Neuroscience (miscellaneous)
    Masruha Marcelo R; Caboclo Luis O S F; Carrete HENRIQUE; Iscia Teresinha Lopes CENDES; Rodrigues Murilo G et al. 2006. Mutation in filamin a causes periventricular heterotopia; developmental regression; and west syndrome in males. Epilepsia (copenhagen). 47, (1) 211-214.
  208. Life Sciences Neurology
    Ruocco Heloísa H; Iscia Teresinha Lopes CENDES; Laurito Tiago L; Li Li M; Fernando CENDES. 2006. Clinical presentation of juvenile huntington disease. Arquivos de neuro-psiquiatria. 64, (1) 5-9.
  209. Health Sciences Neurology (clinical)
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Cláudia V Maurer MORELLI; Simone APPENZELLER; Anamarli NUCCI et al. 2006. Clinical; neuroimaging and genetic findings in hereditary spastic paraplegia with thin corpus callosum (hsp-tcc). Neurology. Estados Unidos. 66, (5) A276-A276.
  210. Health Sciences Neurology (clinical)
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Simone APPENZELLER; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2006. Magnetic resonance spectroscopy (mrs) findings in machado-joseph disease. Neurology. Estados Unidos. 66, (5) A287-A287.
  211. Life Sciences Neurology
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Assessment of the international ataxia rating scale and the unified multiple system atrophy rating scale in machado-joseph disease (mjd). Neurology. Estados Unidos. 66, (5) A287-A287.
  212. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2006. Investigação das epilepsias generalizadas idiopáticas por neuroimagem. Journal of epilepsy and clinical neurophysiology. Brasil. 1, (2) 24-25.
  213. Life Sciences Neuroscience (miscellaneous)
    Fábio Rossi TORRES; Rodrigo SECOLIN; Neide F SANTOS; Marina Coelho GONSALVES; J A F SARDINHA et al. 2006. Epilepsia do lobo temporal autossômica dominante (eltad): procurando o segundo locus responsável. Journal of epilepsy and clinical neurophysiology. Brasil. 12, (2) 63-63.
  214. Life Sciences Neurology
    Vinícius D Avila Bittencourt PASCHOAL; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Luís E G G BETTING; Neide F SANTOS; Carlos Alberto Mantovani GUERREIRO et al. 2006. Epilepsia mioclônica juvenil (emj): identificação de mutações no gene efhc1. Journal of epilepsy and clinical neurophysiology. Brasil. 12, (2) 63-64.
  215. Life Sciences Genetics
    Simone Sayuri TSUNEDA; Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES et al. 2006. Estudo de mecanismo mutacional no gene fln1 em pacientes portadores de heterotopia nodular periventricular bilateral (hnpb). Journal of epilepsy and clinical neurophysiology. Brasil. 12, (2) 64-64.
  216. Health Sciences Medicine (miscellaneous)
    Cláudia V Maurer MORELLI; Rodrigo SECOLIN; Romenia Ramos DOMINGUES; Rafael B MARCHESINI; Neide F SANTOS et al. 2006. Identificação de um locus para a epilepsia de lobo temporal mesial familiar através do estudo de ligação genômico. Journal of epilepsy and clinical neurophysiology. Brasil. 12, (2) 64-64.
  217. Health Sciences Pediatrics, Perinatology and Child Health
    Alberto Luiz Cunha Da COSTA; Carlos Alberto Mantovani GUERREIRO; Maria Augusta S MONTENEGRO; Iscia Teresinha Lopes CENDES; Vera Lúcia G S LOPES. 2006. Malformações e alterações de desenvolvimento em filhos de mães com epilepsia. Journal of epilepsy and clinical neurophysiology. Brasil. 12, (2) 64-65.
  218. Life Sciences Neuroscience (miscellaneous)
    Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO; Lourenço SBRAGIA; Rovilson GIGLIOLI; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Possível função para o gene lgi1 sugerido pelo padrão de expressão em cérebros de roedores. Journal of epilepsy and clinical neurophysiology. Brasil. 12, (2) 65-65.
  219. Life Sciences Neuroscience (miscellaneous)
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Do Carmo De Souza RODRIGUES; Maria Augusta S MONTENEGRO et al. 2006. Triagem de mutações em um grupo de pacientes com distúrbios do desenvolvimento cortical. Journal of epilepsy and clinical neurophysiology. Brasil. 12, (2) 65-65.
  220. Health Sciences Medicine (miscellaneous)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2006. Carbamazepina e epilepsias generalizadas idiopáticas. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 82-82.
  221. Life Sciences Neuroscience (miscellaneous)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2006. Investigação das focalidades em pacientes com epilepsia generalizada idiopática utilizando a morfometria baseada em voxel. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 89-89.
  222. Health Sciences Medicine (miscellaneous)
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Cláudia V Maurer MORELLI; Simone APPENZELLER; A ALESSIO et al. 2006. Magnetic resonance imaging in the assessment of hereditary spastic paraplegia with thin corpus callosum. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 140-140.
  223. Life Sciences Genetics
    M M RODRIGUES; R S PINHO; V K P R FARIAS; H Carrete JUNIOR; L O S CABOCLO et al. 2006. Mutation in filamin a causes periventricular heterotopia; developmental regression; and west syndrome in males. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 209-209.
  224. Life Sciences Neurology
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Anamarli NUCCI; Iscia Teresinha Lopes CENDES. 2006. Clinical and neurophysiological spectrum of peripheral neuropathy in machado-joseph disease. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 217-217.
  225. Health Sciences Neurology (clinical)
    A WOLF; L F MOURÃO; R M MEDEIROS; D S SANTOS; Marcondes Cavalcante França JUNIOR et al. 2006. Deglutição da doença de machado-joseph: estudo de 3 casos. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 246-246.
  226. Health Sciences Neurology (clinical)
    A WOLF; L F MOURÃO; R M MEDEIROS; D S SANTOS; Marcondes Cavalcante França JUNIOR et al. 2006. Diadococinesia fonoarticulatória na doença de machado-joseph: dados preliminares. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 247-247.
  227. Life Sciences Neurology
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2006. Evaluation of patients with machado-joseph disease by the international ataxia rating scale and the unified multiple system atrophy rating scale. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 249-249.
  228. Health Sciences Medicine (miscellaneous)
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2006. Sllepiness and sleep disturbance in patients with machado-joseph disease. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 259-259.
  229. Social Sciences & Humanities Psychology (miscellaneous)
    P A T KIMAID; A WOLF; D S SANTOS; L F MOURÃO; A N CRESPO et al. 2006. Tremor vocal essencial: avaliação de 3 casos de uma família. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 261-261.
  230. Health Sciences Neurology (clinical)
    Anelyssa Cysne Frota D ABREU; Marcondes Cavalcante França JUNIOR; Simone APPENZELLER; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2006. White matter dysfunction in machado-joseph disease. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 262-262.
  231. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2006. Eeg features in idiopathic generalized epilepsy: clues to diagnosis. Epilepsia (copenhagen). 47, (3) 523-528.
  232. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2006. Mri volumetry shows increased anterior thalamic volumes in patients with absence seizures. Epilepsy & behavior. 8, 575-580.
  233. Life Sciences Neurology
    Marcondes Cavalcante França JUNIOR; Maria E CALCAGNOTTO; Jaderson C Da COSTA; Iscia Teresinha Lopes CENDES. 2006. Spinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family. Movement disorders. 21, (7) 1051-1053.
  234. Life Sciences Neuroscience (miscellaneous)
    Ruocco H H; Iscia Teresinha Lopes CENDES; Li L M; Santos Silva M; F CENDES. 2006. Striatal and extrastriatal atrophy in huntington's disease and its relationship with length of the cag repeat. Brazilian journal of medical and biological research. 39, (8) 1129-1136.
  235. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Susana Barreto MORY; Li Li MIN; Iscia Teresinha Lopes CENDES; Marilisa Mantovani GUERREIRO et al. 2006. Voxel-based morphometry in patients with idiopathic generalized epilepsies. Neuroimage (orlando). 32, 498-502.
  236. Life Sciences Genetics
    Cláudia V Maurer MORELLI; Rodrigo SECOLIN; Rafael B MARCHESINI; Neide F SANTOS; Eliane KOBAYASHI et al. 2006. The scn2a gene is not a likely candidate for familial mesial temporal lobe epilepsy. Epilepsy research. 71, 233-236.
  237. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Bertelli D F; Araujo E P; Cesquini M; Stoppa G R; Gasparotto Contessotto M et al. 2006. Phosphoinositide-specific inositol polyphosphate 5-phosphatase iv inhibits inositide trisphosphate accumulation in hypothalamus and regulates food intake and body weight. Endocrinology (philadelphia). 147, 5385-5399.
  238. Life Sciences Neuroscience (miscellaneous)
    Marcondes Cavalcante França JUNIOR; Anelyssa Cysne Frota D ABREU; Veronica A ZANARDI; A V FARIA; Iscia Teresinha Lopes CENDES et al. 2006. Spinal cord mri is a useful diagnostic and prognostic tool in the assessment of chronic sensory neuronopathies. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 228-228.
  239. Life Sciences Neurology
    Lopes C F; F CENDES; Piovesana A M S G; Fr TORRES; Iscia Teresinha Lopes CENDES et al. 2006. Epileptic features of patients with unilateral and bilateral schizencephaly. Journal of child neurology. 21, (9) 757-760.
  240. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2006. Mri reveals structural abnormalities in patients with idiopathic generalized epilepsy. Neurology (cleveland; ohio). 67, (5) 848-852.
  241. Health Sciences Medicine (miscellaneous)
    Melo Áurea Nogueira DE; Yakubian Elza MÁRCIA; Iscia Teresinha Lopes CENDES; Fontenelle Lucia Da COSTA; Teixeira Wagner AFONSO et al. 2005. A inserção da epilepsia no ensino médico (graduação). Journal of epilepsy and clinical neurophysiology (impresso). 11, 7-10.
  242. Life Sciences Neuroscience (miscellaneous)
    A L COSTA; Iscia Teresinha Lopes CENDES; C A GUERREIRO. 2005. Seizure frequency during pregnancy and the puerperium. International journal of gynaecology and obstetrics. 88, 148-149.
  243. Life Sciences Genetics
    Neide F SANTOS; Iara Leda Brandão De ALMEIDA; Rodrigo SECOLIN; Fernando CENDES; Marilisa Mantovani GUERREIRO et al. 2005. A new candidate locus for bilateral perisylvian polymicrogyria on chromosome xq27-q28. Epilepsia. Estados Unidos. 46, (6) 95-95.
  244. Health Sciences Neurology (clinical)
    Vinícius D Avila Bittencourt PASCHOAL; Patrícia Aline Oliveira RIBEIRO; L E BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2005. Frequency of mutations in the efhc1 gene in a large group of patients with juvenile myoclonic epilepsy. Epilepsia. Estados Unidos. 46, (6) 255-256.
  245. Life Sciences Genetics
    Steiner Carlos EDUARDO; Marilisa Mantovani GUERREIRO; Antonia Paula Marques De FARIA; Iscia Teresinha Lopes CENDES. 2005. Laboratorial diagnosis of fragile-x syndrome: experience in a sample of individuals with pervasive developmental disorders. Arquivos de neuro-psiquiatria. 63, (3-A) 564-570.
  246. Health Sciences Medicine (miscellaneous)
    L E BETTING; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2005. Mri investigation of the thalamus in patients with absense epilepsy. Arquivos de neuro-psiquiatria. Brasil. 46, (6) 175-175.
  247. Life Sciences Neurology
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Augusta S MONTENEGRO; Juan Clinton LLERENA et al. 2005. Mutation screening in genes for cortex development in patients with cortical malformations. Epilepsia. Estados Unidos. 46, (6) 96-96.
  248. Life Sciences Neuroscience (miscellaneous)
    Fábio Rossi TORRES; Rodrigo SECOLIN; Neide F SANTOS; Eliane KOBAYASHI; Luis A C SARDINHA et al. 2005. Searching for a new locus for autosomal dominant lateral temporal lobe epilepsy (adl tle). Epilepsia. Estados Unidos. 46, (6) 257-257.
  249. Health Sciences Genetics (clinical)
    Celso Eduardo BENEDETTI; Maria Cristina Cabral GARCIA; Iscia Teresinha Lopes CENDES; C L P OLIVEIRA; Iris C L TORRIANI. 2005. Changes in molecular conformation of expanded ataxin-3: experimental evidence from small angle x-ray scatering (saxs) technique. Activity report / brazilian synchrotron light laboratory. Brasil. 1, -.
  250. Health Sciences Neurology (clinical)
    Luís E G G BETTING; Suzana B MORY; Iscia Teresinha Lopes CENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2005. Eeg features in idiopathic generalized epilepsy: clues to diagnosis. Epilepsia. Estados Unidos. 46, (8) 133-133.
  251. Life Sciences Genetics
    Daniela Aguiar De SOUZA; Fábio Rossi TORRES; Camila Fernanda LOPES; Maria Augusta S MONTENEGRO; Juan Clinton LLERENA et al. 2005. Frequency of mutations in candidate genes in a large cohort of patients with cortical malformations. Epilepsia. Estados Unidos. 46, (8) 271-271.
  252. Life Sciences Neurology
    Patrícia Aline Oliveira RIBEIRO; Vinícius D Avila Bittencourt PASCHOAL; Luís E G G BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2005. Juvenile myoclonic epilepsy and chromosome 6p: a new candidate locus?. Epilepsia. Estados Unidos. 46, (8) 370-370.
  253. Life Sciences Genetics
    Neide F SANTOS; Iara Leda Brandão De ALMEIDA; Rodrigo SECOLIN; Marilza Santos SILVA; Fernando CENDES et al. 2005. Linkage analysis of bilateral perisylvian polymicrogyria: a new candidate locus on chromosome xq27-q28. Epilepsia. Estados Unidos. 46, (8) 370-370.
  254. Health Sciences Medicine (miscellaneous)
    Áurea Nogueira De MELLO; Elza Márcia Targas YACUBIAN; Iscia Teresinha Lopes CENDES; Lucia Da Costa FONTENELLE; Wagner Afonso TEIXEIRA et al. 2005. Epilepsy education in medical school (undergraduate). Journal of epilepsy and clinical neurophysiology. Brasil. 11, (4 -Suppl 1) 7-10.
  255. Life Sciences Neurology
    Fernando CENDES; KOBAYASHI; Iscia Teresinha Lopes CENDES. 2005. Familial temporal lobe epilepsy with auditory features. Epilepsia (copenhagen). 46, (Suppl 10) 59-60.
  256. Social Sciences & Humanities Psychology (miscellaneous)
    Herrera Eliane P; Brandão Almeida Iara L; Guimarães Catarina A; Oliveira Ecila P M; Montenegro Maria AUGUSTA et al. 2005. Síndrome peri-sylviana: estudo de uma família brasileira com ênfase na modalidade de transmissão genética e espectro clínico. Arquivos de neuro-psiquiatria. 63, 459-463.
  257. Life Sciences Neuroscience (miscellaneous)
    Maria Augusta Santos MONTENEGRO; Demet KINAY; Fernando CENDES; Andrea BERNASCONI; Neda BERNASCONI et al. 2004. Patterns of hippocampal abnormalities in malformations of cortical development. Archives of neurology (chicago). Estados Unidos. 1, 1-1.
  258. Social Sciences & Humanities Psychology (miscellaneous)
    Eliane Provenzano HERRERA; Iara ALMEIDA; Catarina Abraão GUIMARÃES; Ecila Paula Dos MESQUITA; Maria Augusta Santos MONTENEGRO et al. 2004. Síndrome perisylviana: estudo de uma família brasileira com ênfase na modalidade de transmissão genética e espectro clínico. Arquivos de neuro-psiquiatria. Brasil. 1, 1-1.
  259. Health Sciences Neurology (clinical)
    Maria Augusta Santos MONTENEGRO; Marilisa Mantovani GUERREIRO; Iscia Teresinha Lopes CENDES; Carlos A M GUERREIRO; Li Li MIN et al. 2004. Variable presentation and severity of epilepsy in the different types of malformations of cortical development. Neuropediatrics. Estados Unidos. 1, 1-.
  260. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2004. Expansão de poliglutaminas e doenças neurodegenerativas. Ciência e cultura (sbpc). Brasil. 56, (1) 27-28.
  261. Life Sciences Genetics
    Fábio Rossi TORRES; Maria Augusta MONTENEGRO; Antonia Paula MARQUESDEFARIA; Marilisa M GUERREIRO; Fernando CENDES et al. 2004. Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia. Neurology (cleveland; ohio). Estados Unidos. 62, 799-802.
  262. Health Sciences Medicine (miscellaneous)
    Iara Leda BRANDÃOALMEIDA; Simone R V HAGE; Catarina A GUIMARÃES; Neide F SANTOS; Ecila P M OLIVIEIRA et al. 2004. Polimicrogiria perisylviana bilateral congênita: aspectos clínicos; eletrencefalográficos; neurorradiológicos; psicolinguísticos e genéticos. Journal of epilepsy and clinical neurophysiology. Brasil. 10, 7-12.
  263. Health Sciences Medicine (miscellaneous)
    Coan A C; E KOBAYASHI; Iscia Teresinha Lopes CENDES; Li L M; F CENDES. 2004. Abnormalities of hippocampal signal intensity in patients with familial mesial temporal lobe epilepsy. Brazilian journal of medical and biological research. 37, (6) 827-832.
  264. Life Sciences Neurology
    S F BERKOVIC; J M SERRATOSA; H A PHILLIPS; L XIONG; E ANDERMANN et al. 2004. Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12. Epilepsia (copenhagen). 45, 1054-1060.
  265. Health Sciences Neurology (clinical)
    A ALESSIO; E KOBAYASHI; B P DAMASCENO; Iscia Teresinha Lopes CENDES; F CENDES. 2004. Evidence of memory impairment in asymptomatic individuals with hippocampal atrophy. Epilepsy & behavior. 6, 981-987.
  266. Health Sciences Neurology (clinical)
    L E BETTING; S B MORY; P A O RIBEIRO; Iscia Teresinha Lopes CENDES; L M LI et al. 2004. Mri voxel-based-morphometry in patients with idiopathic generalized epilepsies. Revista mexicana de neurociencia. México. 5, (3) 191-.
  267. Health Sciences Neurology (clinical)
    R B MARCHESINI; C V MAURERMORELLI; N F SANTOS; R SECOLIN; E KOBAYASHI et al. 2004. Voltage-gated potassium channels in familial mesial temporal lobe epilepsy. Revista mexicana de neurociencia. México. 5, (3) 193-.
  268. Health Sciences Pediatrics, Perinatology and Child Health
    Karine Couto Sarmento TEIXEIRA; Maria Augusta S MONTENEGRO; Iara Leda Brandão De ALMEIDA; Iscia Teresinha Lopes CENDES; Fernando CENDES et al. 2004. Clinical features of patients with polymicrogyria. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 192-192.
  269. Health Sciences Neurology (clinical)
    Camila Fernanda LOPES; Fernando CENDES; Maria Augusta S MONTENEGRO; Fábio Rossi TORRES; Iscia Teresinha Lopes CENDES et al. 2004. Epileptic form of unilateral and bilateral schizencephalies. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 233-233.
  270. Life Sciences Neurology
    L E BETTING; Mfr ROSA; Susana Barreto MORY; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Generalized tonic-clonic seizures: clinical and eeg features. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 40-40.
  271. Health Sciences Genetics (clinical)
    H TEIVE; W O ARRUDA; Salmo RASKIN; Iscia Teresinha Lopes CENDES; A FREUND et al. 2004. Genotype-phenotype correlation in 100 families with spinocerebellar ataxias. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 11-11.
  272. Health Sciences Neurology (clinical)
    Eliane KOBAYASHI; Simone APPENZELLER; Susana Barreto MORY; Li Li MIN; Iscia Teresinha Lopes CENDES et al. 2004. Hippocampal 1h mrs findings in patients familial mesial temporal lobe epilepsy. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 73-73.
  273. Health Sciences Neurology (clinical)
    L E BETTING; Susana Barreto MORY; Patrícia Aline Oliveira RIBEIRO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Mri findings in patients with idiopathic generalized epilepsy. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 7-7.
  274. Life Sciences Genetics
    Eliane Provenzano HERRERA; Iara Leda Brandão De ALMEIDA; Catarina A GUIMARÃES; Ecila P M OLIVIEIRA; Maria Augusta S MONTENEGRO et al. 2004. Perisylvian syndrome: report of one brazilian family with focus on the genetic mode of inheritance and clinical spectrum. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 179-179.
  275. Life Sciences Neurology
    Heloisa Helena RUOCCO; Iscia Teresinha Lopes CENDES; Li Li MIN; Fernando CENDES. 2004. Quantification of basal ganglia; cerebral and cerebellar atrophy by volumetric mri i patients with huntington disease. association with length of the cag repeat. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 7-7.
  276. Health Sciences Neurology (clinical)
    L E BETTING; Susana Barreto MORY; Patrícia Aline Oliveira RIBEIRO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Thalamic volumetry in juvenile myoclonic epilepsy. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 6-6.
  277. Health Sciences Neurology (clinical)
    L E BETTING; Susana Barreto MORY; Patrícia Aline Oliveira RIBEIRO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Voxel-based morphometry in patients with idiopathic generalized epilepsy: influence of genetic predisposition. Arquivos de neuro-psiquiatria. Brasil. 62, (2) 41-41.
  278. Life Sciences Neuroscience (miscellaneous)
    Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2004. A new fln1 mutation in a family segregating bilateral periventricular nodular heterotopia (bpnh). Revista mexicana de neurociência. México. 5, (3) 221-221.
  279. Life Sciences Genetics
    Antonia Paula Marques De FARIA; Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES et al. 2004. A new lis1 missense mutation in a patient with the lissencephaly/subcortical band heterotopia spectrum. Revista mexicana de neurociência. México. 5, (3) 217-217.
  280. Life Sciences Genetics
    Maria Augusta S MONTENEGRO; Maria Do Carmo De Souza RODRIGUES; Fábio Rossi TORRES; Ana Maria S G PIOVESANA; Marilisa Mantovani GUERREIRO et al. 2004. Emx2 and schizencephaly: mutation screening in a group of 33 patients. Revista mexicana de neurociência. México. 5, (3) 217-217.
  281. Health Sciences Neurology (clinical)
    Iara Leda Brandão De ALMEIDA; Marilisa Mantovani GUERREIRO; Neide F SANTOS; Fábio Rossi TORRES; Rodrigo SECOLIN et al. 2004. Familial perisylvian polymicrogyria clinical features; genetic in investigation and mri findings. Revista mexicana de neurociência. México. 5, (3) 193-193.
  282. Life Sciences Genetics
    Rodrigo SECOLIN; Neide F SANTOS; Eliane KOBAYASHI; Fábio Rossi TORRES; L A C SARDINHA et al. 2004. Genetic studies in autosomal dominant lateral temporal lobe epilepsy. Revista mexicana de neurociência. México. 5, (3) 218-218.
  283. Health Sciences Neurology (clinical)
    Cláudia V Maurer MORELLI; Neide F SANTOS; Rodrigo SECOLIN; Rafael B MARCHESINI; Eliane KOBAYASHI et al. 2004. Genome-wide search in familial mesial temporal lobe epilepsy. Revista mexicana de neurociência. México. 5, (3) 218-218.
  284. Life Sciences Neurology
    P M PRETO; Alberto Luiz Cunha Da COSTA; Iscia Teresinha Lopes CENDES; Carlos Alberto Mantovani GUERREIRO. 2004. Perinatal aspects in offspring of womem with epilepsy. Revista mexicana de neurociência. México. 5, (3) 216-216.
  285. Life Sciences Neuroscience (miscellaneous)
    Alberto Luiz Cunha Da COSTA; Li Li MIN; Iscia Teresinha Lopes CENDES; Carlos Alberto Mantovani GUERREIRO. 2004. Seizure frequency during pregnancy and puerperium. Revista mexicana de neuriciência. México. 5, (3) 216-216.
  286. Life Sciences Neuroscience (miscellaneous)
    Vinícius D Avila Bittencourt PASCHOAL; Patrícia Aline Oliveira RIBEIRO; Luís E G G BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2004. The role of chromosome 6p in juvenile myoclonic epilepsy. Revista mexicana de neurociência. México. 5, (3) 221-221.
  287. Life Sciences Neurology
    Patrícia Aline Oliveira RIBEIRO; Luís E G G BETTING; Neide F SANTOS; Vinícius D Avila Bittencourt PASCHOAL; Rodrigo SECOLIN et al. 2004. The role of gabra 1 gene and the 5q34 chromosome region in the etiology of juvenile myoclonic epilepsy. Revista mexicana de neurociência. México. 5, (3) 195-195.
  288. Health Sciences Medicine (miscellaneous)
    Cláudia V Maurer MORELLI; Neide F SANTOS; Rafael B MARCHESINI; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2004. Análise de ligação em genes candidadtos para canais de potássio na epilepsia de lobo temporal mesial familiar (eltmf). Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 13-13.
  289. Health Sciences Neurology (clinical)
    Rafael B MARCHESINI; Cláudia V Maurer MORELLI; Neide F SANTOS; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2004. Análise de ligação em região candidata do cromossomo 3 para epilepsia do lobo temporal mesial familiar. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 16-16.
  290. Health Sciences Medicine (miscellaneous)
    Rodrigo SECOLIN; R G M FERREIRA; Cláudia V Maurer MORELLI; Neide F SANTOS; Eliane KOBAYASHI et al. 2004. Análise de segregação em famílias com epilepsia de lobo temporal mesial familiar. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 16-16.
  291. Health Sciences Medicine (miscellaneous)
    Alberto Luiz Cunha Da COSTA; P M PRETO; Iscia Teresinha Lopes CENDES; Carlos Alberto Mantovani GUERREIRO. 2004. Aspectos perinatais em filhos de mães com epilepsia. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 30-30.
  292. Life Sciences Neuroscience (miscellaneous)
    Luís E G G BETTING; Susana Barreto MORY; Patrícia Aline Oliveira RIBEIRO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Avaliação de pacientes com epilepsia generalizada idiopática através da morfometria baseada em voxel. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 25-25.
  293. Health Sciences Psychiatry and Mental Health
    Camila Fernanda LOPES; Fernando CENDES; Maria Augusta S MONTENEGRO; Fábio Rossi TORRES; Iscia Teresinha Lopes CENDES et al. 2004. Características da epilepsia na infância em pacientes com esquizencefalia unilateral versus bilateral. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 32-32.
  294. Health Sciences Genetics (clinical)
    H A G TEIVE; W O ARRUDA; Salmo RASKIN; Iscia Teresinha Lopes CENDES; L C WERNECK. 2004. Correlação genotípica-fenotípica em 100 famílias com ataxias espinocerebelares. O dendrito. Brasil. 10, (2) 34-34.
  295. Life Sciences Neurology
    Luís E G G BETTING; Susana Barreto MORY; Patrícia Aline Oliveira RIBEIRO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Eeg inicial e seriado em pacientes com epilepsia generalizada idiopática. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 40-40.
  296. Health Sciences Neurology (clinical)
    Maria Isabel C R MORAIS; Marilisa Mantovani GUERREIRO; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2004. Epilepsias mioclônicas progressivas: diagnóstico histopatológico e molecular. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 15-15.
  297. Life Sciences Neurology
    Vinícius D Avila Bittencourt PASCHOAL; Patrícia Aline Oliveira RIBEIRO; Luís E G G BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2004. Estudos de ligação e associações das regiões cromossômicas 6p21 em epilepsia mioclônica juvenil. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 16-16.
  298. Health Sciences Genetics (clinical)
    Fábio Rossi TORRES; Maria Do Carmo De Souza RODRIGUES; Maria Augusta S MONTENEGRO; Ana Maria S G PIOVESANA; Marilisa Mantovani GUERREIRO et al. 2004. O gene emx2 e esquizencefalia: procura de mutações em um grande grupo de pacientes. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 13-13.
  299. Health Sciences Neurology (clinical)
    Patrícia Aline Oliveira RIBEIRO; Luís E G G BETTING; Vinícius D Avila Bittencourt PASCHOAL; Neide F SANTOS; Rodrigo SECOLIN et al. 2004. O papel do gene gabra1 e da região cromossômica 5q34 na epilepsia mioclônica juvenil e outras formas de epilepsia generalizada idiopática. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 15-15.
  300. Life Sciences Neuroscience (miscellaneous)
    Cláudia V Maurer MORELLI; Neide F SANTOS; Rafael B MARCHESINI; Rodrigo SECOLIN; Eliane KOBAYASHI et al. 2004. Progressos nos estudos de ligação visando a identificação do gene responsável pela epilepsia de lobo temporal mesial familiar (eltmf). Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 13-13.
  301. Life Sciences Neurology
    Iara Leda Brandão De ALMEIDA; Marilisa Mantovani GUERREIRO; Neide F SANTOS; Fábio Rossi TORRES; Rodrigo SECOLIN et al. 2004. Síndrome perisylviana bilateral congênita: características clínicas; investigação genética e achados de neuroimagem. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 14-14.
  302. Health Sciences Medicine (miscellaneous)
    Fabio Thadeu FERREIRA; Eliane KOBAYASHI; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2004. Structural abnormalities are similar in familial and nonfamilial mesial temporal lobe epilepsy. Canadian journal of neurological sciences. 10, (2) 368-372.
  303. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Fábio Rossi TORRES; Maria Augusta S MONTENEGRO; Marilisa Mantovani GUERREIRO; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2004. Uma nova mutação no gene fln1 em uma família segregando heterotopia nodular periventricular bilateral. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 13-13.
  304. Life Sciences Neurology
    Luís E G G BETTING; Susana Barreto MORY; Patrícia Aline Oliveira RIBEIRO; Iscia Teresinha Lopes CENDES; Li Li MIN et al. 2004. Volumetria do tálamo em pacientes com epilepsia mioclônica juvenil. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (2) 40-40.
  305. Health Sciences Genetics (clinical)
    H TEIVE; W O ARRUDA; Salmo RASKIN; Iscia Teresinha Lopes CENDES; L C WERNECK. 2004. Genotype-phenotype correlation in 100 families with spinocerebellar ataxias. Neurology. Estados Unidos. 62, (Supl 5) 31-31.
  306. Health Sciences Neurology (clinical)
    Patrícia Aline Oliveira RIBEIRO; Neide F SANTOS; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2004. Aspectos genéticos da epilepsia mioclônica juvenil: consenso e controvérsia. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 10, (1) 27-32.
  307. Life Sciences Genetics
    Fábio Rossi TORRES; Maria Augusta MONTENEGRO; Antonia Paula Marques De FARIA; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2003. Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia. Neurology. 9 (62), (in press) 799-802.
  308. Health Sciences Neurology (clinical)
    Patrícia A O RIBEIRO; Luís E G G BETTING; Neide F SANTOS; Eliane KOBAYASHI; Suzana B MORY et al. 2003. The relevance of gabra1 gene mutations in juvenile myoclonic epilepsy and other forms of idiopathic generalized epilepsy. Neurology. Estados Unidos. 60, (supl 1) A92-A92.
  309. Health Sciences Neurology (clinical)
    Neide F SANTOS; Eliane KOBAYASHI; Fabio R TORRES; Rodrigo SECOLIN; Luis A F SARDINHA et al. 2003. Familial temporal lobe epilepsy with auditory auras: clinical and genetic heterogeneity. Neurology. Estados Unidos. 60, (supl 1) A277-A277.
  310. Health Sciences Medicine (miscellaneous)
    Eliane KOBAYASHI; Ana C COAN; Iscia Teresinha Lopes CENDES; Li M LI; F CENDES. 2003. Abnormalities of hippocampal signal intensity in patients with familial mesial temporal lobe epilepsy. Neurology. Estados Unidos. 60, (supl 1) A279-A279.
  311. Life Sciences Genetics
    Fabio R TORRES; Maria A MONTENEGRO; Marilisa GUERREIRO; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2003. Fln1 mutations in patients with atypical periventricular nodular heterotopia. Neurology. Estados Unidos. 60, (supl 1) A279-A279.
  312. Life Sciences Neuroscience (miscellaneous)
    Heloisa Helena RUOCCO; Iscia Teresinha Lopes CENDES; Marilza Santos SILVA; Maura VIANA; Elisabete QUAGLIATO et al. 2003. Quantification of caudate and putamen atrophy by volumetric mri in patients with huntington disease: association between length of the cag repeat and age at onset. Neurology. Estados Unidos. 60, (supl 1) A286-A286.
  313. Social Sciences & Humanities Education
    Maria Fernanda Ribeiro ROSA; Iscia Teresinha Lopes CENDES. 2003. Conhecendo o sujeito de pesquisa: um estudo piloto. O mundo da saúde. Brasil. 27, (4) 499-503.
  314. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 2003. Genética das epilepsias. Comciência. 34, 145-147.
  315. Life Sciences Neurology
    Eliane KOBAYASHI; Iscia Teresinha Lopes CENDES; F CENDES. 2003. Epilepsia de lobo temporal: síndrome ou grupo de síndromes?. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 9, 41-47.
  316. Health Sciences Neurology (clinical)
    Maria Isabel C R MORAIS; Fernando CENDES; Marilisa Mantovani GUERREIRO; Luciano De Souza QUEIROZ; Maria Letícia CINTRA et al. 2003. Epilepsias mioclônicas progressivas: aspectos clínicos e genéticos. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 9, (2) 115-123.
  317. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES. 2003. Genetics of focal epilepsies. Arquivos de neuro-psiquiatria. Brasil. 61, (2) 19-22.
  318. Health Sciences Medicine (miscellaneous)
    Gisele Resende Coelho CASELATO; Eliane KOBAYASHI; Leonardo BONILHA; Gabriela CASTELLANO; Ares Hawatha RIGAS et al. 2003. Hippocampal texture analysis in patients with familial mesial temporal lobe epilepsy. Arquivos de neuro-psiquiatria. Brasil. 61, (2) 83-87.
  319. Health Sciences Neurology (clinical)
    Eliane KOBAYASHI; Maria Daniella D AGOSTINO; Iscia Teresinha Lopes CENDES; Samuel F BERKOVIC; Li Min LI et al. 2003. Hippocampal atrophy and t2-weighted signal changes in familial mesial temporal lobe epilepsy. Neurology (cleveland; ohio). Estados Unidos. 60, 405-410.
  320. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2003. Genes e epilepsia. O dendrito. Brasil. 9, (1) 4-7.
  321. Health Sciences Genetics (clinical)
    Fábio Rossi TORRES; Antonia Paula Marques De FARIA; Maria Augusta MONTENEGRO; Marilisa M GUERREIRO; Fernando CENDES et al. 2003. A new missense mutation in a patient with classic lissencephaly. Epilepsia. Estados Unidos. 44, (9) 70-71.
  322. Life Sciences Neurology
    Marcelo M RODRIGUES; Luis Otávio S F CABLOCO; Eliana GARZON; Henrique C JÚNIOR; Fábio Rossi TORRES et al. 2003. Autosomal recessive form of periventricular nodular heterotopia in three brothers with west syndrome. Epilepsia. Estados Unidos. 44, (9) 71-71.
  323. Health Sciences Genetics (clinical)
    Fábio Rossi TORRES; Maria Do Carmo S RODRIGUES; Maria Augusta MONTENEGRO; Ana Maria S G PIOVESANA; Marilisa M GUERREIRO et al. 2003. Searching for mutations in the emx2 gene in a large sample of patients with schizencephaly. Epilepsia. Estados Unidos. 44, (9) 72-72.
  324. Life Sciences Neuroscience (miscellaneous)
    Claudia V MAURERMORELLI; Neide F SANTOS; Rodrigo SECOLIN; Rafael B MARCHESINI; Eliane KOBAYASHI et al. 2003. Linkage study of voltage-gated potassium channels in familial temporal lobe epilepsy: a progress report. Epilepsia. Estados Unidos. 44, (9) 242-242.
  325. Life Sciences Neurology
    Neide F SANTOS; Rodrigo SECOLIN; Fábio Rossi TORRES; Eliane KOBAYASHI; Luiz A F SARDINHA et al. 2003. Relationship between lgi1 mutations; mri abnormalities and clinical status in familial temporal lobe epilepsy with auditory auras. Epilepsia. Estados Unidos. 44, (9) 243-243.
  326. Life Sciences Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
    Eva ANDERMANN; Susan DUNCAN; Suha MERCHO; Iscia Teresinha Lopes CENDES; Marie Helene SENI et al. 2003. Safety of carbamazepine exposure during pregnancy. Epilepsia. Estados Unidos. 44, (8) 35-35.
  327. Health Sciences Medicine (miscellaneous)
    Susan DUNCAN; Suha MERCHO; Iscia Teresinha Lopes CENDES; Marie Helene SENI; Linda DANSKY et al. 2003. The effect of valproic acid on the outcome of pregnancy: a prospective study. Epilepsia. Estados Unidos. 44, (8) 59-59.
  328. Health Sciences Neurology (clinical)
    L E BETTING; S B MORY; P A O RIBEIRO; L M LI; C A M GUERREIRO et al. 2003. Associated cinical conditions and seizure control in idiopathic generalized epilepsy. Epilepsia. Estados Unidos. 44, (8) 158-158.
  329. Life Sciences Neurology
    Maria Isabel C R MORAIS; Fabio Rossi TORRES; Daniela Medeiros De CASTRO; Fernando CENDES; Luciano De Souza QUEIROZ et al. 2003. Clinical and molecular studies in progressive myoclonic epilepsy. Epilepsia. Estados Unidos. 44, (8) 74-74.
  330. Health Sciences Neurology (clinical)
    Iara Leda Brandão De ALMEIDA; Iscia Teresinha Lopes CENDES; Marilisa M GUERREIRO; Neide F SANTOS; Catarina GUIMARAES et al. 2003. Clinical features and mri findings associated with familial congenital bilateral perisylvian syndrome. Epilepsia. Estados Unidos. 44, (8) 90-90.
  331. Life Sciences Neurology
    Iara Leda Brandão De ALMEIDA; Marilisa M GUERREIRO; Neide F SANTOS; C A GUIMARAES; S R HAGE et al. 2003. Familial congenital perisylvian syndrome: clinical spectrum and neuroimaging findings. American journal of human genetics. Estados Unidos. 73, (suppl) 273-273.
  332. Life Sciences Neuroscience (miscellaneous)
    Fabio Rossi TORRES; Maria Augusta MONTENEGRO; Marilisa M GUERREIRO; Fernando CENDES; Iscia Teresinha Lopes CENDES. 2003. Confirmation of genetic heterogeneity in subcortical band heterotopia. American journal of human genetics. Estados Unidos. 73, (suppl) 294-294.
  333. Health Sciences Neurology (clinical)
    Neide F SANTOS; Rodrigo SECOLIN; Eliane KOBAYASHI; L A C SARDINHA; Fernando CENDES et al. 2003. A new lfi1 mutation in familial temporal epilepsy with auditory auras. American journal of human genetics. Estados Unidos. 73, (suppl) 471-471.
  334. Health Sciences Neurology (clinical)
    Claudia V MAURERMORELLI; Neide F SANTOS; Rodrigo SECOLIN; Rafael B MARCHESINI; Eliane KOBAYASHI et al. 2003. Linkage studies of familial mesial temporal lobe epilepsy: a progress report. American journal of human genetics. Estados Unidos. 73, (suppl) 478-478.
  335. Health Sciences Medicine (miscellaneous)
    Patrícia Aline O RIBEIRO; Vinícius D B PASCOAL; Luis E BETTING; Neide F SANTOS; Rodrigo SECOLIN et al. 2003. Linkage and association studies of the controversial locus 6p21 in idiopathic generalized epilepsies (ige). American journal of human genetics. Estados Unidos. 73, (suppl) 501-501.
  336. Health Sciences Neurology (clinical)
    Eliane KOBAYASHI; N F SANTOS; R F TORRES; R SECOLIN; L A F SARDINHA et al. 2003. Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras. Archives of neurology (chicago). 60, (11) 1546-1551.
  337. Health Sciences Neurology (clinical)
    Eliane KOBAYASHI; M D D AGOSTINO; Iscia Teresinha Lopes CENDES; E ANDERMANN; F DUBEAU et al. 2003. Outcome of surgical treatment in familial mesial temporal lobe epilepsy. Epilepsia (copenhagen). 44, (8) 1080-1084.
  338. Life Sciences Neuroscience (miscellaneous)
    Ruocco HH; Silva MS; Laurito TL; Viana MA; Quagliato EMBA et al. 2002. Quantificação da atrofia do caudato e putamen por rnm volumétrica em pacientes com doença de huntington: relação entre repetição do cag expandido e idade de início. Arquivos brasileiros de neuropsiquiatria. Brasil. 60, (supl 1) 31-31.
  339. Life Sciences Neuroscience (miscellaneous)
    Silva HC; Pires ABA; Iscia Teresinha Lopes CENDES; Callegaro D; Zanoteli E. 2002. Deleção do gene smn2 em pacientes com esclerose lateral amiotrófica (ela). Arquivos brasileiros de neuropsiquiatria. Brasil. 60, (supl 1) 37-38.
  340. Life Sciences Neuroscience (miscellaneous)
    Leone AAA; Cendes F; Kobayashi E; Damasceno BP; Iscia Teresinha Lopes CENDES. 2002. Relevância da atrofia hipocampal e frequencia de crises no déficit de memória em pacientes com epilepsia de lobo temporal familial. Arquivos brasileiros de neuropsiquiatria. Brasil. 60, (supl 1) 41-41.
  341. Life Sciences Neurology
    N F SANTOS; F R TORRES; L A F SARDINHA; F CENDES; Iscia Teresinha Lopes CENDES. 2002. Clinical and genetic heterogeneity in familial temporal lobe epilepsy. Epilepsia. Estados Unidos. 43, (supl 5) 133-133.
  342. Health Sciences Medicine (miscellaneous)
    Kobayashi E; D Agostino MD; Iscia Teresinha Lopes CENDES; Andermann E; Dubeau F et al. 2002. Outcome of surgical treatment in patients with familial mesial temporal lobe epilepsy. Neurology. Estados Unidos. 58, (supl 3) A95-A95.
  343. Health Sciences Neurology (clinical)
    Kobayashi E; Leone AA; Damasceno BP; Iscia Teresinha Lopes CENDES; Li ML et al. 2002. Neuropsychological evaluation in patients with familial mesial temporal lobe epilepsy. Neurology. Estados Unidos. 58, (supl 3) A122-A122.
  344. Health Sciences Neurology (clinical)
    Montenegro MA; Guerreiro MM; Guerreiro CAM; Iscia Teresinha Lopes CENDES; Li ML et al. 2002. Family history of epilepsy anticipates seizure onset in focal cortical dysplasia. Neurology. Estados Unidos. 58, (supl 3) A123-A123.
  345. Life Sciences Neuroscience (miscellaneous)
    Kobayashi E; Iscia Teresinha Lopes CENDES; Li ML; F CENDES. 2002. Hippocampal atrophy in asymptomatic first-degree relatives of patientes with familial mesial temporal lobe epilepsy (fmtle). Neurology. Estados Unidos. 58, (supl 3) A150-A150.
  346. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; F CENDES. 2002. Interrelationship of genetics and prenatal injury in the genesis of malformations of cortical development. Archives of neurology (chicago). 59, 1147-1153.
  347. Health Sciences Medicine (miscellaneous)
    E KOBAYASHI; D FACCHIN; C E STEINER; A A Alves LEONE; N L V CAMPOS et al. 2002. Mesial temporal lobe abnormalities in a family with 15q26qter trisomy. Archives of neurology (chicago). 59, 1476-1479.
  348. Life Sciences Neurology
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; C Am GUERREIRO; L M LI et al. 2002. Association of family history of epilepsy with earlier age at seizure onset in patients with focal cortical dysplasia. Mayo clinic proceedings. Estados Unidos. 77, 1-4.
  349. Health Sciences Neurology (clinical)
    Kobayashi E; Iscia Teresinha Lopes CENDES; Li M LI; F CENDES. 2002. Magnetic resonance imaging evidence of hippocampal sclerosis in asymptomatic first degree relatives of patients with familial mesial temporal lobe epilepsy. Archives of neurology (chicago). 59, 1891-1894.
  350. Life Sciences Neuroscience (miscellaneous)
    D Agostino MD; Bernasconi A; Das S; Bastos A; Valerio RM et al. 2002. Subcortical band heterotopia (sbh) in males: clinical; imaging and genetic findings in comparison to females. Brain (london). Grã-Bretanha. 125, 2507-2522.
  351. Health Sciences Neurology (clinical)
    Kobayashi E; D Agostino MD; Iscia Teresinha Lopes CENDES; Berkovic SF; Li LM et al. 2002. Hippocampal atrophy and t2-weighted signal changes in familial mesial temporal lobe epilepsy. Neurology (cleveland; ohio). Estados Unidos. 60, 405-409.
  352. Life Sciences Neuroscience (miscellaneous)
    Fabio Rossi TORRES; Iscia Teresinha Lopes CENDES. 2002. Aspectos genéticos das malformações do desenvolvimento cortical. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 8, 163-170.
  353. Life Sciences Neurology
    Santos N F; Sousa S C; Kobayashi E; Torres F R; Sardinha J A F et al. 2002. Clinical and genetic heterogeneity in familial temporal lobe epilepsy. Epilepsia (copenhagen). 43, 136-136.
  354. Life Sciences Genetics
    S DUNCAN; S MERCHO; Iscia Teresinha Lopes CENDES; M H SENI; A BENJAMIM et al. 2001. Repeated neural tube defects and valproate monotherapy suggest a pharmacogenetic abnormality. Epilepsia (copenhagen). 42, 750-753.
  355. Life Sciences Neurology
    M A MONTENEGRO; F CENDES; L M LI; C A M GUERREIRO; Iscia Teresinha Lopes CENDES et al. 2001. História familiar de epilepsia antecipa a idade da primeira crise epiléptica em pacientes com displasia cortical focal. Arquivos brasileiros de neuropsiquiatria. Brasil. 59, (supl 2) 27-27.
  356. Health Sciences Neurology (clinical)
    L E BETTING; E KOBAYASHI; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; L M LI et al. 2001. Epilepsia de lobo temporal mesial benigna: estudo comparativo entre casos esporádicos e familiares. Arquivos brasileiros de neuropsiquiatria. Brasil. 59, (supl 2) 29-29.
  357. Health Sciences Neurology (clinical)
    E KOBAYASHI; F T FERREIRA; Iscia Teresinha Lopes CENDES; F CENDES. 2001. Estudo volumétrico do lobo temporal em pacientes com epilepsia de lobo temporal mesial familiar (eltmf). Arquivos brasileiros de neuropsiquiatria. Brasil. 59, (supl 2) 36-36.
  358. Life Sciences Genetics
    D FACCHIN; S A ANTONIUK; I BRUCK; L JARDIM; J C COSTA et al. 2001. Correlação entre análise de haplótipos e linkage em casos familiais de síndrome de rett. Arquivos brasileiros de neuropsiquiatria. Brasil. 59, (supl 1) 161-162.
  359. Health Sciences Neurology (clinical)
    M I C R MORAIS; D M De CASTRO; M M GUERREIRO; F CENDES; Iscia Teresinha Lopes CENDES. 2001. Avaliação sistemática dos pacientes com epilepsia mioclônica progressiva. Arquivos brasileiros de neuropsiquiatria. Brasil. 59, (supl 1) 164-164.
  360. Life Sciences Neurology
    N F SANTOS; S C SOUSA; E KOBAYASHI; F R TORRES; J A F SARDINHA et al. 2001. Evidence for linkage between one family with lateral temporal lobe epilepsy and chromosome 10q. Epilepsia. Estados Unidos. 42, (supl 2) 79-79.
  361. Health Sciences Neurology (clinical)
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; F CENDES. 2001. Variable severity of epilepsy in different types of malformation of cortical development. Epilepsia. Estados Unidos. 42, (supl 2) 15-15.
  362. Life Sciences Neurology
    M A MONTENEGRO; F CENDES; L M LI; C A M GUERREIRO; Iscia Teresinha Lopes CENDES et al. 2001. Positive family history for epilepsy anticipates age of first seizure in patients with focal cortical dysplasia. American journal of human genetics. Estados Unidos. 69, (supl) 281-281.
  363. Health Sciences Neurology (clinical)
    D FACCHIN; E KOBAYASHI; F CENDES; C E STEINER; A A A LEONE et al. 2001. Mesial temporal lobe abnormalities in a family with 15q26qter trisomy. American journal of human genetics. Estados Unidos. 69, (supl) 279-279.
  364. Health Sciences Medicine (miscellaneous)
    R S R PAIVA; Iscia Teresinha Lopes CENDES. 2001. Molecular testing for late onset neurodegenerative disorders: a health care professionals perspective. American journal of human genetics. Estados Unidos. 69, (supl) 428-428.
  365. Health Sciences Neurology (clinical)
    E KOBAYASHI; N F SANTOS; F R TORRES; R SECOLIN; La F SARDINHA et al. 2001. Mri abnormalities in familial temporal lobe epilepsy with auditory auras. Epilepsia. Estados Unidos. 42, (supl 7) 63-63.
  366. Health Sciences Neurology (clinical)
    H A G TEIVE; F M IWAMOTO; C H CAMARGO; Iscia Teresinha Lopes CENDES; L C WERNECK. 2001. Machado-joseph disease versus hereditary spastic paraplegia: case report. Arquivos de neuro-psiquiatria. 59, 809-811.
  367. Health Sciences Medicine (miscellaneous)
    H A G TEIVE; C H CAMARGO; F M IWAMOTO; G FABIANI; Iscia Teresinha Lopes CENDES et al. 2001. Ataxia por deficiência de vitamina e. O dendrito. Brasil. 7, 75-78.
  368. Health Sciences Neurology (clinical)
    E KOBAYASHI; Iscia Teresinha Lopes CENDES; M M GUERREIRO; C A M GUERREIRO; F CENDES. 2001. Seizure outcome and hippocampal atrophy in familial mesial temporal lobe epilepsy. Neurology (cleveland; ohio). Estados Unidos. 56, 166-172.
  369. Life Sciences Genetics
    C GASPAR; Iscia Teresinha Lopes CENDES; S HAYES; G A ROULEAU. 2001. Ancestral origins of the machado-joseph disease mutation: a word wide haplotype study. American journal of human genetics. 68, 523-528.
  370. Health Sciences Neurology (clinical)
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; F CENDES. 2001. Bilateral posterior parietal polymicrogyria: a mild form of congenital bilateral perisylvian syndrome ?. Epilepsia (copenhagen). 42, 845-849.
  371. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; F CENDES; Iscia Teresinha Lopes CENDES; M M GUERREIRO. 2001. The contribution of genetic and prenatal events in the etiology of different forms of cortical malformation. Epilepsia. Estados Unidos. -.
  372. Health Sciences Neurology (clinical)
    E C ETCHEBEHERE; F CENDES; Iscia Teresinha Lopes CENDES; José Antonio PEREIRA; Maria Cristina Lins LIMA et al. 2001. Brain single-photon emission computed tomography and magnetic resonance imaging in machado-joseph disease. Archives of neurology (chicago). 58, 1257-1263.
  373. Life Sciences Neurology
    Eliane KOBAYASHI; Daniela FACCHIN; Carlos Eduardo STAINER; Andréa A Alves LEONE; Nilma Lúcia V CAMPOS et al. 2001. Mesial temporal lobe abnormalities in a family with 15q26qter trisomy. Neurology. Estados Unidos. -.
  374. Life Sciences Neurology
    N F SANTOS; S C SOUSA; E KOBAYASHI; F R TORRES; L A F SARDINHA et al. 2001. Clinical and genetic heterogeneity in familial temporal lobe epilepsy. Neurology. Estados Unidos. 56, A154-.
  375. Health Sciences Neurology (clinical)
    E KOBAYASHI; F ANDERMANN; L M LI; Iscia Teresinha Lopes CENDES; E ANDERMANN et al. 2001. Volumetric studies in familial mesial temporal lobe epilepsy. Neurology. Estados Unidos. 56, A153-.
  376. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; F CENDES. 2001. Relevance of genetic and prenatal events in different forms of malformations of cortical development. Neurology. Estados Unidos. 56, A135-.
  377. Life Sciences Neurology
    N F SANTOS; S C SOUSA; E KOBAYASHI; F R TORRES; L A F SARDINHA et al. 2001. Clinical and genetic heterogeneity in familial temporal lobe epilepsy. Epilepsy research. Estados Unidos. -.
  378. Life Sciences Neurology
    N F SANTOS; S C SOUSA; E KOBAYASHI; F R TORRES; L A F SARDINHA et al. 2001. Evidence for linkage between one family with lateral temporal lobe epilepsy and chromosome 10q. Epilepsia. Estados Unidos. 42, 79-79.
  379. Health Sciences Neurology (clinical)
    M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; F CENDES. 2001. Variable severity of epilepsy in different types of malformation of cortical development. Epilepsia. Estados Unidos. 42, 15-15.
  380. Health Sciences Neurology (clinical)
    Maria Augusta MONTENEGRO; M M GERREIRO; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; Li Min LI et al. 2001. Family history of epilepsy anticipates seizure onset in patients with focal cortical dysplasia. Neurology. Estados Unidos. -.
  381. Health Sciences Neurology (clinical)
    F CARDOSO; M PUCCIONISOHLER; A R FERNANDES; Iscia Teresinha Lopes CENDES; J P MATTOS et al. 2000. Eyelid dystonia in machado-joseph disease. Movement disorders. Estados Unidos. 15, 1028-1030.
  382. Life Sciences Neurology
    Tc Lima E SILVA; H G SERRA; C S BERTUZZO; Iscia Teresinha Lopes CENDES. 2000. Molecular diagnosis of huntington disease in brazilian patients. Arquivos de neuro-psiquiatria. 58, 11-17.
  383. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES; I E SCHEFFER; S F BERKOVIC; M ROUSSEAU; E ANDERMANN et al. 2000. A new locus for idiopathic generalized epilepsy with febrile seizures plus maps to chromosome 2. American journal of human genetics. 66, 698-701.
  384. Life Sciences Neurology
    E KOBAYASHI; F CENDES; S C SOUSA; A E SCOTONI; M I CARVALHO et al. 2000. Epilepsias parciais familiares. Arquivos de neuro-psiquiatria. 58, 862-868.
  385. Life Sciences Genetics
    S HAYES; G TURECKI; K BRISEBOIS; Iscia Teresinha Lopes CENDES; C GASPAR et al. 2000. Cag repeat length in rai1 is associated with age at onset variability in spinocerebellar ataxia type 2 (sca2). Human molecular genetics. Estados Unidos. 9, 1753-1758.
  386. Health Sciences Neurology (clinical)
    E C ETCHEBEHERE; Iscia Teresinha Lopes CENDES; F CENDES; J PEREIRA; M LIMA et al. 2000. Brain spect and magnetic resonance imaging in machado-joseph disease. Journal of nuclear medicine. Estados Unidos. 41, 223-223.
  387. Health Sciences Neurology (clinical)
    E KOBAYASHI; F CENDES; S C SOUSA; C A M GUERREIRO; M M GUERREIRO et al. 2000. Familial temporal lobe epilepsy with hippocampal atrophy is not linked to chromosome 10q. Epilepsia. Estados Unidos. 41, 73-73.
  388. Health Sciences Neurology (clinical)
    Maria Augusta MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; F CENDES. 2000. Bilateral posterior parietal polymicrogyria: a mild form of congenital bilateral perisylvian syndrome?. Epilepsia. Estados Unidos. 41, 100-101.
  389. Life Sciences Neuroscience (miscellaneous)
    E KOBAYASHI; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; B P DAMASCENO; D HONORATO et al. 2000. Tratamento cirúrgico em pacientes com epilepsia de lobo temporal familiar. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 6, 121-121.
  390. Life Sciences Neurology
    S C SOUSA; E KOBAYASHI; F CENDES; Iscia Teresinha Lopes CENDES. 2000. Epilepsia de lobo temporal mesial não apresenta ligação no cromossomo 10q. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 6, 121-121.
  391. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; M M GERREIRO; Iscia Teresinha Lopes CENDES; F CENDES. 2000. Disgenesias corticais: contribuição de fatores genéticos e ambientais na sua etiologia. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 6, 122-122.
  392. Health Sciences Pediatrics, Perinatology and Child Health
    M M GERREIRO; M A MONTENEGRO; Iscia Teresinha Lopes CENDES; W FERNANDES; P S PACHECO et al. 2000. Síndrome perisilviana familiar. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 6, 122-122.
  393. Life Sciences Neurology
    E KOBAYASHI; D FACCHIN; F CENDES; C E STEINER; A A A LEONE et al. 2000. Epilepsia generalizada secundária em pacientes com trissomia parcial 15q26-qter. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 6, 122-122.
  394. Life Sciences Genetics
    D M CASTRO; M I C R MORAIS; L S FERREIRA; M A MONTENEGRO; M M GERREIRO et al. 2000. Mutação a3243g no mtdna como causa de epilepsia sintomática. Anais do congresso brasileiro de genética clínica. Brasil. 1, 19-19.
  395. Health Sciences Genetics (clinical)
    D FACCHIN; S ANTONIUK; I BRUCK; J C COSTA; L JARDIM et al. 2000. Clonagem posicional na região xq28 em 23 famílias de pacientes com síndrome de rett. Genetics and molecular biology. Brasil. 23, 277-278.
  396. Health Sciences Medicine (miscellaneous)
    C E STEINER; M E R CAMARGO; T C L SILVA; D FACCHIN; A P MARQUESDEFARIA et al. 2000. Triagem para a mutação fraxa pela técnica da pcr em 50 indivíduos com distúrbios invasivos do desenvolvimento. Genetics and molecular biology. Brasil. 23, 279-279.
  397. Health Sciences Medicine (miscellaneous)
    M F A G CAMARGO; H A G TEIVE; Iscia Teresinha Lopes CENDES. 2000. Estudo das frequências das ataxias espinocerebelares autossômicas dominantes em uma amostra da população brasileira. Genetics and molecular biology. Brasil. 23, 287-287.
  398. Health Sciences Medicine (miscellaneous)
    S C SOUSA; E KOBAYASHI; M M GERREIRO; C A M GUERREIRO; F CENDES et al. 2000. Estudo de ligação genética em epilepsia de lobo temporal mesial. Genetics and molecular biology. Brasil. 23, 287-287.
  399. Life Sciences Genetics
    D M De CASTRO; M I C R MORIAS; D FACCHIN; L S FERREIRA; M A MONTENEGRO et al. 2000. Estudo de freqüência de mutações de ponto no mtdna em um grupo de pacientes com suspeita clínica de doença mitocondrial. Genetics and molecular biology. Brasil. 23, 292-293.
  400. Life Sciences Genetics
    T C L SILVA; M E R CAMARGO; C S BERTUZZO; Iscia Teresinha Lopes CENDES. 2000. Análise da sequência polimórfica (ccg)n localizada na região 3'ajusante do gene it15 em cromossomos normais da população brasileira. Genetics and molecular biology. Brasil. 23, 299-299.
  401. Life Sciences Genetics
    F C COSTA; T C L SILVA; H G SERRA; M S SILVA; Iscia Teresinha Lopes CENDES. 2000. Aspectos moleculares das ataxias espinocerebelares autossômicas recessivas. Genetics and molecular biology. Brasil. 23, 558-558.
  402. Life Sciences Neuroscience (miscellaneous)
    A C COAN; E KOBAYASHI; F CENDES; Iscia Teresinha Lopes CENDES. 2000. Alteração de sinal hipocampal em pacientes com epilepsia de lobo temporal familiar. Arquivos de neuro-psiquiatria. Brasil. 58, 10-10.
  403. Health Sciences Medicine (miscellaneous)
    E KOBAYASHI; D FACCHIN; F CENDES; C E STEINER; A A A LEONE et al. 2000. Epilepsia secundária e deficiência mental relacionadas a alterações citogenéticas. Arquivos de neuro-psiquiatria. Brasil. 58, 11-11.
  404. Health Sciences Neurology (clinical)
    E KOBAYASHI; S C SOUSA; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; M M GERREIRO et al. 2000. Epilepsia de lobo temporal familiar associada a atrofia hipocampal. Arquivos de neuro-psiquiatria. Brasil. 58, 11-11.
  405. Health Sciences Medicine (miscellaneous)
    S C SOUSA; E KOBAYASHI; M M GERREIRO; C A M GUERREIRO; F CENDES et al. 2000. Exclusão de ligação entre 18 loci candidatos para epilepsia em famílias com epilepsia de lobo temporal mesial. Arquivos de neuro-psiquiatria. Brasil. 58, 12-12.
  406. Life Sciences Genetics
    D FACCHIN; S ANTONIUK; I BRUCK; J C COSTA; L B JARDIM et al. 2000. Estudos moleculares na síndrome de rett. Arquivos de neuro-psiquiatria. Brasil. 58, 20-20.
  407. Life Sciences Genetics
    M F A G CAMARGO; F C COSTA; M A VIANA; E M A B QUAGLIATO; A NUCCI et al. 2000. O diagnóstico molecular das ataxias espinocerebelares em uma grande amostra de pacientes brasileiros. Arquivos de neuro-psiquiatria. Brasil. 58, 21-21.
  408. Health Sciences Neurology (clinical)
    Eliane KOBAYASHI; Fernando CENDES; S C SOUSA; A E SCOTONI; M I CARVALHO et al. 2000. [familial partial epilepsies]. Arquivos de neuro-psiquiatria. Brasil. 58, (3-B) 862-868.
  409. Social Sciences & Humanities Psychology (miscellaneous)
    R S R PAIVA; F NORONHA; Iscia Teresinha Lopes CENDES. 2000. Motivações para a realização do teste molecular diagnóstico em pacientes com doenças neurodegenerativas de início tardio: a visão do paciente. Arquivos de neuro-psiquiatria. Brasil. 58, 21-21.
  410. Life Sciences Genetics
    E C S C ETCHEBEHERE; F CENDES; Iscia Teresinha Lopes CENDES; M C L LIMA; C D RAMOS et al. 2000. Spect cerebral e ressonância magnética na doença de machado-joseph. Arquivos de neuro-psiquiatria. Brasil. 58, 96-96.
  411. Life Sciences Neuroscience (miscellaneous)
    M A MONTENEGRO; M M GERREIRO; F CENDES; Iscia Teresinha Lopes CENDES. 2000. Fatores de risco para a ocorrência de polimicrogiria parietal posterior bilateral. Arquivos de neuro-psiquiatria. Brasil. 58, 100-100.
  412. Health Sciences Medicine (miscellaneous)
    C E STEINER; M E R CAMARGO; T C L SILVA; D FACCHIN; Iscia Teresinha Lopes CENDES et al. 2000. Screening for the fraxa mutation using the pcr technique in a sample of individuals with pervasive disorders of development. Arquivos de neuro-psiquiatria. Brasil. 58, 101-101.
  413. Social Sciences & Humanities Language and Linguistics
    A BACELAR; O BACELAR; Iscia Teresinha Lopes CENDES. 2000. Doença de machado-joseph: relato de um caso. Arquivos de neuro-psiquiatria. Brasil. 58, 102-102.
  414. Health Sciences Medicine (miscellaneous)
    H A G TEIVE; F IWAMOTO; C H CAMARGO; Iscia Teresinha Lopes CENDES; L C WERNECK. 2000. Doença de machado-joseph e paraplegia espástica hereditária. Arquivos de neuro-psiquiatria. Brasil. 58, 102-102.
  415. Life Sciences Neurology
    S A UNES; C J LEÃO; M A C ALVES; I F GUIMARÃES; V D FRANCO et al. 2000. Ataxia hereditária autossômica dominante tipo 1. Arquivos de neuro-psiquiatria. Brasil. 58, 103-103.
  416. Life Sciences Genetics
    T C L SILVA; M S SILVA; M A VIANA; E M A B QUAGLIATO; N BECKER et al. 2000. Confirmação molecular da doença de huntington em pacientes brasileiros. Arquivos de neuro-psiquiatria. Brasil. 58, 104-104.
  417. Life Sciences Genetics
    H C A SILVA; H G SERRA; M S SILVA; João Paulo S Nogueira LIMA; D CALLEGARO et al. 2000. Análise molecular no diagnóstico diferencial da doença de kennedy. Arquivos de neuro-psiquiatria. Brasil. 58, 104-104.
  418. Life Sciences Genetics
    D M CASTRO; M I C R MORAIS; D FACCHIN; W O BRAGANÇA; L S FERREIRA et al. 2000. Pesquisa de mutações de ponto no mtdna em um grupo de pacientes com suspeita clínica de doença mitocondrial. Arquivos de neuro-psiquiatria. Brasil. 58, 104-104.
  419. Health Sciences Neurology (clinical)
    S KANEKO; D BATTINO; E ANDERMANN; K WADA; R KAN et al. 1999. Congenital malformations due to antiepileptic drugs. Epilepsy research. Estados Unidos. 33, 145-158.
  420. Health Sciences Neurology (clinical)
    D BATTINO; S KANEKO; E ANDERMANN; G AVANZINI; M P CANEVINI et al. 1999. Intrauterine growth in the offspring of epileptic women: a prospective multicenter study. Epilepsy research. Estados Unidos. 36, 53-60.
  421. Life Sciences Genetics
    P MACIEL; C GASPAR; L GUIMARÃES; J GOTO; Iscia Teresinha Lopes CENDES et al. 1999. Study of three intragenic polymorphisms in the machado-joseph disease gene (mjd1) in relation to genetic instability of the (cag)n tract. European journal of human genetics. Estados Unidos. 147-156.
  422. Life Sciences Neuroscience (miscellaneous)
    R JOOBER; C BENKELFAT; M JANNATIPOUR; G TURECKI; S LAL et al. 1999. Polyglutamine-containing proteins in schizophrenia. Molecular psychiatry. Estados Unidos. 4, 53-57.
  423. Health Sciences Neurology (clinical)
    I Lopes CENDES; E KOBAYASHI; S C De SOUSA; T C L SILVA; A E SCOTONI et al. 1999. Familial temporal lobe epilepsy: clinical and genetic studies. Neurology. Estados Unidos. 52(2), A546-.
  424. Life Sciences Neurology
    E KOBAYASHI; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; F CENDES. 1999. Mri abnormalities in familial temporal lobe epilepsy. Neurology. Estados Unidos. 52(2), A545-.
  425. Health Sciences Genetics (clinical)
    H G SERRA; H C A SILVA; T C L SILVA; M S SILVA; D CALLEGARO et al. 1999. Análise molecular no diagnóstico diferencial da doença de kennedy. Genetics and molecular biology. Brasil. 22, 248-.
  426. Life Sciences Genetics
    M F A G CAMARGO; Iscia Teresinha Lopes CENDES. 1999. Aspectos moleculares das ataxias espinocerebelares autossômicas dominantes na população brasileira. Genetics and molecular biology. Brasil. 22, 247-.
  427. Life Sciences Neuroscience (miscellaneous)
    T C L SILVA; H G SERRA; C S BERTUZZO; Iscia Teresinha Lopes CENDES. 1999. Caracterização molecular da doença de huntington na população brasileira. Genetics and molecular biology. Brasil. 22, 244-.
  428. Life Sciences Genetics
    F C COSTA; T C L SILVA; M S SILVA; Iscia Teresinha Lopes CENDES. 1999. Caracterização molecular da ataxia de friedreich na população brasileira: o uso de dois pares de primers. Genetics and molecular biology. Brasil. 22, 233-.
  429. Health Sciences Neurology (clinical)
    S C SOUSA; E KOBAYASHI; C A M GUERREIRO; F CENDES; Iscia Teresinha Lopes CENDES. 1999. Estudos de ligação em epilepsia de lobo temporal familiar. Genetics and molecular biology. Brasil. 22, 222-.
  430. Life Sciences Neuroscience (miscellaneous)
    E KOBAYASHI; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; M M GUERREIRO; F CENDES. 1999. Eletroencefalograma e ressonância magnética em pacientes com epilepsia de lobo temporal familiar. Arquivos de neuro-psiquiatria. Brasil. 57, (13) 13-.
  431. Health Sciences Neurology (clinical)
    E KOBAYASHI; F CENDES; C A M GUERREIRO; M M GUERREIRO; A E SCOTONI et al. 1999. Familial partial epilepsies. Epilepsia. Estados Unidos. 40, 177-.
  432. Health Sciences Neurology (clinical)
    E KOBAYASHI; Iscia Teresinha Lopes CENDES; A E SCOTONI; M M GUERREIRO; C A M GUERREIRO et al. 1999. Clinical; eeg and mri findings in a large number of families with temporal lobe epilepsy. Epilepsia. Estados Unidos. 40, 266-.
  433. Health Sciences Neurology (clinical)
    Y OHTSUKA; K SILVER; E ANDERMANN; Iscia Teresinha Lopes CENDES; T TSUDA. 1999. Effect of antiepileptic drugs on psychomotor development in offspring of epileptic mothers. Epilepsia. Estados Unidos. 40, 296-.
  434. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1999. Entendendo os princípios básicos dos estudos de genética molecular. Neuro press. Brasil. 3, (1) 3-5.
  435. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1999. Avanços recentes nas doenças heredo-degenerativas do adulto. Neuro press. Brasil. 3, (1) 6-8.
  436. Health Sciences Neurology (clinical)
    F CENDES; Iscia Teresinha Lopes CENDES; E ANDERMANN; F ANDERMANN. 1998. Familial temporal lobe epilepsy: a clinically heterogeneous syndrome. Neurology (cleveland; ohio). Estados Unidos. 50, 554-557.
  437. Health Sciences Neurology (clinical)
    Klockgether T; Iscia Teresinha Lopes CENDES. 1998. The natural history of degenerative ataxia: a retrospective study in 466 patients. Brain (london). 121, 589-600.
  438. Life Sciences Genetics
    S J KISH; Iscia Teresinha Lopes CENDES; M GUTTMAN; Y FURUKAWA; A KOEPPEN et al. 1998. Brain glyceraldehydyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disorders. Archives of neurology (chicago). 55, 1299-1304.
  439. Life Sciences Neuroscience (miscellaneous)
    H A PHILLIPS; I E SCEHFER; K M CROSSLAND; K P BHATIA; C D MARSDEN et al. 1998. Autossomal dominant nocturnal frontal lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24. American journal of human genetics. 63, 1108-1116.
  440. Life Sciences Neurology
    B A MINASSIAN; J R LEE; J J A HERBRICK; S HUIZENGA; A J SODER et al. 1998. Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Nature genetics. 20, 171-174.
  441. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES. 1998. Genética e epilepsia. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 4, (4) 182-187.
  442. Health Sciences Neurology (clinical)
    M D DÁGOSTINO; E ANDERMANN; S F BERKOVIC; I Lopes CENDES; Iscia Teresinha Lopes CENDES et al. 1998. Familial temporal lobe epilepsy (ftle): clinical characterization and preliminary linkage studies. American journal of human genetics. Estados Unidos. 63(sp), A101-.
  443. Health Sciences Neurology (clinical)
    B A MINASSIAN; J LEE; J HERBRICK; J HUIZENGA; A MUNGALL et al. 1998. Molecular genetics of lafora's progressive myoclonus epilepsy. American journal of human genetics. Estados Unidos. 62(sp), A374-.
  444. Health Sciences Neurology (clinical)
    M D DÁGOSTINO; E ANDERMANN; S F BERKOVIC; Iscia Teresinha Lopes CENDES; B Abou KHALIL et al. 1998. Clinical and pedigree analysis in familial temporal lobe epilepsy (ftle). Epilepsia. Estados Unidos. 39(6), 177-.
  445. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    B A MINASSIAN; J LEE; J HERBRICK; J HUIZENGA; A MUNGALL et al. 1998. Towards cloning the lafora's disease gene on chromosome 6q. Epilepsia. Brasil. 39(6), 145-.
  446. Health Sciences Medicine (miscellaneous)
    E KOBAYASHI; S C De SOUSA; T C L SILVA; C A M GUERREIRO; I Lopes CENDES et al. 1998. Epilepsia de lobo temporal familiar. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 4, 85-.
  447. Health Sciences Neurology (clinical)
    E KOBAYASHI; T C L SILVA; S C De SOUSA; C A M GUERREIRO; A E SCOTONI et al. 1998. Epilepsias idiopáticas familiares. Arquivos de neuro-psiquiatria. Brasil. 56(sp), 25-.
  448. Health Sciences Medicine (miscellaneous)
    M F A G CAMARGO; F C COSTA; T C L SILVA; Iscia Teresinha Lopes CENDES. 1998. Avaliação da heterogeneidade clínica e genética em pacientes com ataxia espinocerebelar. Arquivos de neuro-psiquiatria. Brasil. 56(sp), 73-.
  449. Health Sciences Medicine (miscellaneous)
    H TEIVE; D SÁ; W ARRUDA; P TREVISOL; L WERNECK et al. 1998. Pode-se diferenciar a doença de machado-joseph de outras ataxias espinocerebelares baseado em critérios clínicos ?. Arquivos de neuro-psiquiatria. Brasil. 56(sp), 29-.
  450. Life Sciences Neurology
    H TEIVE; W O ARRUDA; P B TREVISOL; L C WERNECK; Iscia Teresinha Lopes CENDES et al. 1998. Is it possible to differentiate machado-joseph disease from other spinocerebellar ataxias based on clinical grounds ?. Movement disorders. Estados Unidos. 13, 85-85.
  451. Life Sciences Genetics
    P MACIEL; Iscia Teresinha Lopes CENDES; S KISH; J SEQUEIROS; G A ROULEAU. 1997. Mosaicism of the cag repeat in cns tissue in relation to age at death in sca1 and mjd patients. American journal of human genetics. Estados Unidos. 60, 993-999.
  452. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; H G A TEIVE; M E CALCAGNOTTO; J C Da COSTA; F CARDOSO et al. 1997. Frequency of the different mutations causing spinocerebellar ataxia (sca1; sca2; mjd/sca3 and drpla) in a large group of brazilian patients. Arquivos de neuro-psiquiatria. Brasil. 55, (3-B) 519-529.
  453. Health Sciences Genetics (clinical)
    Iscia Teresinha Lopes CENDES; H G A TEIVE; F CARDOSO; E VIANA; M E CALCAGNOTTO et al. 1997. Molecular characteristics of machado-joseph disease mutation in 25 newly described brazilian families. Brazilian journal of genetics (impresso). 20, 717-724.
  454. Life Sciences Neurology
    Y ROBITAILLE; Iscia Teresinha Lopes CENDES; M PANDOLFO; S LEDOUX; P DESJARDINS et al. 1997. The neuropathology of triplet repeat diseases: review and update of genetic and molecular mechanisms. Brain pathology. Estados Unidos. 7, 901-926.
  455. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1997. Controvérsias em epilepsia: epilepsia e gestação. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 3, (4) 155-156.
  456. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; A NECHIPORUK; E ATTIG; S BOSH et al. 1997. Frequency and molecular characteristics of the spinocerebellar ataxia type 2 mutation. Neurology. Estados Unidos. 48(2), A177-.
  457. Life Sciences Genetics
    H A G TEIVE; Iscia Teresinha Lopes CENDES; W O ARRUDA; P C B TREVISOL; I Lopes CENDES et al. 1997. Spinocerebellar ataxia: a genetics study in 30 brazilian families. Neurology. Estados Unidos. 48(2), A177-.
  458. Life Sciences Neuroscience (miscellaneous)
    K SILVER; Y OHTSUKA; Iscia Teresinha Lopes CENDES; E ANDERMANN. 1997. Neurological and developmental abnormalities in the offspring of epileptic mother. Epilepsia. Irlanda. 38(3), 252-.
  459. Health Sciences Pharmacology (medical)
    R JOOBER; C BENKELFAT; J L MANDEL; Iscia Teresinha Lopes CENDES; S LAL et al. 1997. Polyglutamine containing proteins in schizophrenia. Biological psychiatry. Estados Unidos. 42, 98S-.
  460. Life Sciences Genetics
    C GASPAR; Iscia Teresinha Lopes CENDES; J GOTO; I Lopes CENDES; S HAYES et al. 1997. Founder effect study in a large group of machado-joseph disease families with different ethnic origins. Journal of neurological sciences. Argentina. 150(sp, S314-.
  461. Life Sciences Neuroscience (miscellaneous)
    P MACIEL; C GASPAR; L GUIMARÃES; A DIAS; K ARVIDSSON et al. 1997. Effect of the normal chromosome on the instability of the expanded cag repeat in the mjd1 gene. Journal of neurological sciences. Argentina. 150, S314-.
  462. Life Sciences Neurology
    P COUTINHO; J GUIMARÃES; J BARROS; J L LOUREIRO; P RIBEIRO et al. 1997. Autosomal dominant ataxias in portugal: review of 106 families. Journal of neurological sciences. Estados Unidos. 150, S40-.
  463. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; F CENDES; E ANDERMANN; F ANDERMANN. 1997. Familial temporal lobe epilepsy: a clinically heterogeneous syndrome. Epilepsia. Estados Unidos. 38(8), 200-.
  464. Life Sciences Genetics
    S PREMKUMAR; Iscia Teresinha Lopes CENDES; A L DESTEFANO; G A ROULEAU; L A FARRER. 1997. Patterns of transmission and correlation between cag repeat and onset age in an ethnically diverse population of spinocerebellar ataxia type 2 (sca2). American journal of human genetics. Estados Unidos. 61(sp), A318-.
  465. Life Sciences Neurology
    S HAYES; Iscia Teresinha Lopes CENDES; E ANDERMANN; C GASPAR; G A ROULEAU. 1997. Investigation of spinocerebellar ataxia type 6 (sca6) in a group of spinocerebellar ataxia patients: frequency; allele distribution and clinical features. American journal of human genetics. Estados Unidos. 61(sp), A310-.
  466. Life Sciences Neurology
    I SILVEIRA; Iscia Teresinha Lopes CENDES; I Lopes CENDES; S KISH; P MACIEL et al. 1996. Frequency of spinocerebellar ataxia type 1; dentatorubropallidoluysian atrophy and machado-joseph disease mutations in a large group of spinocerebellar ataxia patients. Neurology (cleveland; ohio). Estados Unidos. 46, 214-218.
  467. Life Sciences Genetics
    A NECHIPORUK; Iscia Teresinha Lopes CENDES; S STARKMAN; T FREDERICK; E ANDERMANN et al. 1996. Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12. Neurology (cleveland; ohio). Estados Unidos. 46, 1731-1735.
  468. Life Sciences Neuroscience (miscellaneous)
    L K CASAUBON; M MELANSON; Iscia Teresinha Lopes CENDES; C MARINEAU; E ANDERMANN et al. 1996. The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q. American journal of human genetics. Estados Unidos. 58, 28-34.
  469. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; C E STEINER; I SILVEIRA; W Pinto JUNIOR; J A MACIEL et al. 1996. Clinical and molecular characteristics of a brazilian family with spinocerebellar ataxia type 1. Arquivos de neuro-psiquiatria. 54, 412-418.
  470. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; P MACIEL; S KISH; C GASPAR; I SILVEIRA et al. 1996. Somatic mosaicism of the cag repeat length in post-morten cns specimens of spinocerebellar ataxia type 1 (sca 1) and machado-joseph disease (mjd) patients. Annals of neurology. 40, 199-206.
  471. Life Sciences Genetics
    C GASPAR; Iscia Teresinha Lopes CENDES; A DESTEFANO; P MACIEL; I SILVEIRA et al. 1996. Linkage disequilibrium in a group of machado-joseph disease patients of different geographic origins. Human genetics. 98, 620-624.
  472. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; I SILVEIRA; P MACIEL; C GASPAR; J RADVANY et al. 1996. Limits of clinical assessment in the accurate diagnosis of machado-joseph disease. Archives of neurology (chicago). Estados Unidos. 53, 1168-1174.
  473. Life Sciences Genetics
    A S M PULST; T NECHIPORUK; I GISPERT; Xn CHEN; Iscia Teresinha Lopes CENDES et al. 1996. Identification of the sca2 gene: moderate expansion of a normally biallelic trinucleotide repeat. Nature genetics. Estados Unidos. 14, 269-276.
  474. Life Sciences Genetics
    M MELANSON; L CASAUBON; Iscia Teresinha Lopes CENDES; C MARINEAU; E ANDERMANN et al. 1996. The gene responsible for andermann syndrome maps to chromosome 15q. Neurology. Estados Unidos. 46 (2), A272-.
  475. Health Sciences Neurology (clinical)
    P MACIEL; Iscia Teresinha Lopes CENDES; S KISH; C GASPAR; I SILVEIRA et al. 1996. Somatic mosaicism of the cag repeat length in brain specimens of spinocerebellar ataxia type 1 (sca 1) and machado-joseph disease (mjd) patients. Neurology. Estados Unidos. 46(2), A330-.
  476. Life Sciences Genetics
    C GASPAR; Iscia Teresinha Lopes CENDES; A DESTEFANO; P MACIEL; I SILVEIRA et al. 1996. Linkage disequilibrium in a group of machado-joseph disease patients of different geographic origins. Neurology. Estados Unidos. 46(2), A127-.
  477. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; S KISH; I SILVEIRA; Y ROBITAILLE; G A ROULEAU. 1996. Testing cag trinucleotide repeats in post-morten brains from patients with spinocerebellar ataxia: building the bridge between neuropathology and molecular genetics. Neurology. Estados Unidos. 46(2), A329-.
  478. Health Sciences Neurology (clinical)
    G LEONARD; A PTITO; M M H SENI; C VINETTE; S SCHOPFLOCHER et al. 1996. Cognitive outcome in school-age offspring of epileptic mothers exposed to anticonvulsant therapy during pregnancy. Neurology. Estados Unidos. 46(2), A150-.
  479. Health Sciences Neurology (clinical)
    S J KISH; A H KOEPPEN; M NANCE; Iscia Teresinha Lopes CENDES; G A ROULEAU et al. 1996. Brain cholineacetyltransferase activity in sca1; sca2; sca3/mjd; and friedreich's ataxia. Neurology. Estados Unidos. 46(2), A431-.
  480. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; H A G TEIVE; I SILVEIRA; J A MACIEL; J RADVANY et al. 1996. Frequency of the three mutations causing spinocerebellar ataxia (sca1; mjd/sca3 and drpla) in brazilian patients. Brazilian journal of genetics. Brasil. 19(sp), A174-.
  481. Life Sciences Genetics
    P MACIEL; Iscia Teresinha Lopes CENDES; S KISH; J SEQUEIROS; G A ROULEAU. 1996. Somatic mosaicism of the cag repeat length in cns: correlations with pathology and age at death. Brazilian journal of genetics. Brasil. 19(sp), A173-.
  482. Life Sciences Genetics
    C GASPAR; Iscia Teresinha Lopes CENDES; A De STEFANO; P MACIEL; I SILVEIRA et al. 1996. Linkage disequilibrium analysis in machado-joseph disease patients of brazilian origin. Brazilian journal of genetics. Brasil. 19(sp), A172-.
  483. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; I E SCHEFFER; S F BERKOVIC; M ROUSSEAU; E ANDERMANN et al. 1996. Mapping a locus for idiopathic generalized epilepsy in a large multiplex family. Epilepsia. Estados Unidos. 37(5), 127-.
  484. Health Sciences Medicine (miscellaneous)
    C GASPAR; Iscia Teresinha Lopes CENDES; A L DESTEFANO; P MACIEL; I SILVEIRA et al. 1996. Linkage disequilibrium analysis of mjd1 closely linked markers in machado-joseph disease patients of different ethnic origins. European journal of human genetics. Estados Unidos. 4(S1), 119-.
  485. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; C GASPAR; Y TROTTIER; G A J L MANDEL. 1996. Searching for proteins containing polyglutamine expansions in a large group of spinocerebellar ataxia patients. American journal of human genetics. Estados Unidos. 59(sp), A269-.
  486. Life Sciences Genetics
    C GASPAR; J GOTO; Iscia Teresinha Lopes CENDES; P MACIEL; I SILVEIRA et al. 1996. Haplotype analysis in a large group of machado-joseph disease families with different ethnic backgrounds. American journal of human genetics. Estados Unidos. 59(sp), A218-.
  487. Life Sciences Biochemistry, Genetics and Molecular Biology (miscellaneous)
    A A R ABDULLAH; Iscia Teresinha Lopes CENDES; G A ROULEAU; M TRIFIRO; L PINSKY. 1996. Polyglutamine (polygln)-expanded androgen receptor and several of its gln-expanded fragments are resistant to tryptic proteolysis: a plausible neuronotoxic gain-of-function. American journal of human genetics. Estados Unidos. 59(sp), A194-.
  488. Health Sciences Neurology (clinical)
    A V NECHIPORUK; K P FIGUEROA; S SAHBA; Iscia Teresinha Lopes CENDES; J R KORENBERG et al. 1996. Spinocerebellar ataxia type 2 is caused by expansion of a cag trinucleotide repeat whith is stable in the normal population. American journal of human genetics. Estados Unidos. 59(sp), A48-.
  489. Life Sciences Neuroscience (miscellaneous)
    H C HOWARD; M P DUBÉ; C MARINEAU; L K CASAUBON; M MELANSON et al. 1996. Peripheral neuropathy and agenesis of the corpus callosum: linkage disequilibrium in the french-canadian population of quebec. American journal of human genetics. Estados Unidos. 59(sp), A221-.
  490. Health Sciences Medicine (miscellaneous)
    H A G TEIVE; W O ARRUDA; P C Trevisol BITTENCOURT; Iscia Teresinha Lopes CENDES; I SILVEIRA et al. 1996. Ataxias espinocerebelares: avaliação preliminar de 20 famílias através de estudos com genética molecular. Arquivos de neuro-psiquiatria. Brasil. 54(sp), 252-.
  491. Health Sciences Medicine (miscellaneous)
    I SILVEIRA; Iscia Teresinha Lopes CENDES; S KISH; C E STEINER; W PINTOJUNIOR et al. 1995. Analysis of sca1 and drpla mutations in a large population of spinocerebellar ataxia patients. Neurology. Estados Unidos. 45, A422-A422.
  492. Life Sciences Genetics
    S PUSLT; A NECHIPORUK; T NECHIPORUK; Iscia Teresinha Lopes CENDES; G A ROULEAU et al. 1995. Genetic and physical map of the spinocerebellar ataxia 2 (sca2) region on human chromosome 12. Neurology. Estados Unidos. 45, A422-A422.
  493. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; M ROUSSEAU; C BECK; T SORENSEN et al. 1995. Searching for the gene causing lafora body disease (lbd). Epilepsia. Austrália. 36, S6-S6.
  494. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; I E SCHEFFER; S F BERKOVIC; M ROUSSEAU; J I COCHIUS et al. 1995. Genetic linkage studies in idiopathic generalized epilepsy (ige). Epilepsia. Estados Unidos. 36, S7-S7.
  495. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; F ARRUDA; F CENDES; L V DANSKY et al. 1995. Pregnancy outcome in epileptic women over three decades: the impact of changes in the medical management of epileptic patients. Epilepsia. Estados Unidos. 36, 148-148.
  496. Health Sciences Neurology (clinical)
    E ANDERMANN; G LEONARD; A PTITO; Mh SENI; M VINETTE et al. 1995. Cognitive and neurological sequelae of anticonvulsant (aed) therapy during pregnancy on school-age offspring. Epilepsia. Estados Unidos. 36, 91-91.
  497. Life Sciences Neurology
    S F BERKOVIC; H A PHILLIPS; I E SCHEFFER; Iscia Teresinha Lopes CENDES; K P BHATIA et al. 1995. Genetic heterogeneity in autossomal dominant nocturnal frontal lobe epilepsy. Epilepsia. Estados Unidos. 36, 147-147.
  498. Life Sciences Neurology
    I SILVEIRA; Iscia Teresinha Lopes CENDES; J SEQUEIROS; G A ROULEAU. 1995. Molecular diagnosis of sca1; drpla and mjd mutations in a large group of ataxia patients. American journal of human genetics. Estados Unidos. 57, A228-A228.
  499. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; F ARRUDA; F CENDES; L V DAHSKY; M OGUNI et al. 1995. Decreased prevalence of major malformations in offspring of epileptic women over three decades. American journal of human genetics. Estados Unidos. 57, A127-A127.
  500. Health Sciences Neurology (clinical)
    G LEONARD; A PTITO; M H SENI; M VINETTE; C SCHOPFLOCHER et al. 1995. Cognitive performance in school-age offspring of epileptic mothers exposed to anticonvulsant (aed) therapy during pregnancy. American journal of human genetics. Estados Unidos. 57, A136-a136.
  501. Life Sciences Genetics
    P MACIEL; C GASPAR; I SILVEIRA; Iscia Teresinha Lopes CENDES; A DESTEFANO et al. 1995. Correlação entre genótipo (número de repetições cag) e fenótipo (idade de início e subtipo clínico) e seu valor preditivo na doença de machado-joseph. Revista portuguesa de neurologia. Portugal. 5, 18-19.
  502. Health Sciences Medicine (miscellaneous)
    I SILVEIRA; Iscia Teresinha Lopes CENDES; S KISH; P MACIEL; C GASPAR et al. 1995. Estudo das mutações para a ataxia espinocerebelosa 1 (sca1); degenerescência dentatorubropalidoluisiana (drpla) e doença de machado-joseph (dmj) num grande grupo de doentes com ataxia espinocerebelosa e de diferente origem geográfica e étnica. Revista portuguesa de neurologia. Portugal. 5, 19-19.
  503. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1995. Aspectos genéticos das epilepsias: estudos de genética molecular. Journal of epilepsy and clinical neurophysiology (impresso). 8, 7-14.
  504. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; F ANDERMANN. 1995. Lafora-body disease. Anais da 25a rba saberes e práticas antropológicas desafios para o século xxi. 1, 1-1.
  505. Life Sciences Neurology
    I E SCHEFFER; K BHATIA; Iscia Teresinha Lopes CENDES; D FISH; C D MARSDEN et al. 1995. Autosomal dominant nocturnal frontal lobe epilepsy: a distinctive clinical disorder. Brain (london). Inglaterra. 118, 61-73.
  506. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; H A PHILLIPS; I E SHEFFER; J C MULLEY; R DESBIEN et al. 1995. Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the el-1 mouse locus. Epilepsy research. 22, 227-233.
  507. Life Sciences Genetics
    P MACIEL; C GASPAR; A De STEFANO; I SILVEIRA; P COUTINHO et al. 1995. Correlation between the cag repeat length and clinical features in machado-joseph disease. American journal of human genetics. Estados Unidos. 57, 54-61.
  508. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ATTIG; F CENDES; S BOSCH; M WAGNER et al. 1994. Absence of anticipation in spinocerebellar ataxia (sca) families not linked to (ch) 6p. Neurology. Estados Unidos. 44, A294-A294.
  509. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; J I COCHIUS; F ANDERMANN; T SORENSEN et al. 1994. Lafora body disease (lbd): clinical and genetic studies. Epilepsia. Estados Unidos. 35, 152-152.
  510. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; J C MULLEY; E ANDERMANN; I E SCHEFFER; S BERKOVIC et al. 1994. Genetic linkage studies in familial partial epilepsy: exclusion of the human chromosome regions syntenic to the el-1 mouse locus. American jounal of human genetics. Canadá. 35, A350-A350.
  511. Health Sciences Neurology (clinical)
    M ROUSSEAU; Iscia Teresinha Lopes CENDES; S F BERKOVIC; I E SCHEFFER; J I COCHIUS et al. 1994. Towards identification of an epilepsy gene in a large family with idiopathic generalized epilepsy. American journal of human genetics. Canadá. 35, A352-A352.
  512. Life Sciences Neurology
    J SARRAZIN; Iscia Teresinha Lopes CENDES; L PTACEK; E ANDERMANN; G A ROULEAU. 1994. Locus heterogeneity in autosomal dominant spinocerebellar ataxia: evidence for the existence of a fifth locus. American journal of human genetics. Canadá. 35, A202-A202.
  513. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; A NECHIPORUK; T FREDERICK; G ROULEAU; J WEISSENBACH et al. 1994. Genetic map of the sca2 region on chromosome 12. American journal of human genetics. Canadá. 35, A200-A200.
  514. Life Sciences Neuroscience (miscellaneous)
    M MELANÇON; L CASAUBON; Iscia Teresinha Lopes CENDES; J SARRAZIN; C PREVOST et al. 1994. Homozygocity mapping in andermann's syndrome. American journal of human genetics. Estados Unidos. 35, A350-A350.
  515. Life Sciences Genetics
    F ANDERMANN; E ANDERMANN; S CARPENTER; S LEONBERG; Iscia Teresinha Lopes CENDES et al. 1994. Autosomal dominant kufs'disease: clinical heterogeneity in nine families; and exclusion of linkage to cln1 and cln3 markers in a large american kindred. American journal of human genetics. Canadá. 35, A345-A345.
  516. Health Sciences Neurology (clinical)
    I SILVEIRA; Iscia Teresinha Lopes CENDES; P MACIEL; C GASPAR; E TWIST et al. 1994. Linkage studies in machado-joseph disease of non-portuguese ethnic background. American journal of human genetics. Canadá. 35, A352-A352.
  517. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; E ATTIG; F CENDES; S BOSCH et al. 1994. Confirmation of the sca 2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region. American journal of human genetics. 54, 774-781.
  518. Life Sciences Neurology
    I E SCHEFFER; K BHADIA; Iscia Teresinha Lopes CENDES; D FISH; C D MARSDEN et al. 1994. Autosomal dominant frontal epilepsy: a new syndrome misdiagnosed as a sleep disorder. Lancet. 343, 515-517.
  519. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; K SILVER. 1994. Neurological development in the offspring of women with epilepsy. Ictal the epilepsy newsletter. Inglaterra. 8, 16-19.
  520. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; Guy A ROULEAU. 1994. Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus. Genomics (san diego). 21, 270-274.
  521. Health Sciences Neurology (clinical)
    F CENDES; F ANDERMANN; P GLOOR; A GAMBARDELLA; C WATSON et al. 1994. Relationship between atrophy of amygdala and ictal fear in temporal lobe epilepsy. Brain (london). Inglaterra. 117, 739-746.
  522. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; E ATTIG; F CENDES; M I BOTEZ et al. 1993. Locus heterogeneity in french-canadian families with autosomal dominant spinocerebellar ataxia. Canadian journal of neurological sciences. Canadá. 20, S21-S21.
  523. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; K SILVER; L SIAVALAS; E ANDERMANN. 1993. Head circumference in offspring of epileptic women. Canadian journal of neurological sciences. Canadá. 20, S39-S39.
  524. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; K SILVER; L SIAVALAS; E ANDERMANN. 1993. Minor anomalies in offspring of epileptic women: a controlled blind study. Canadian journal of neurological sciences. Canadá. 20, S39-S39.
  525. Life Sciences Neurology
    J D STEWART; Iscia Teresinha Lopes CENDES; E ANDERMANN. 1993. Autonomic dysfunction in a family with spinocerebellar ataxia. Canadian journal of neurological sciences. Canadá. 20, S20-S20.
  526. Health Sciences Medicine (miscellaneous)
    E ANDERMANN; Iscia Teresinha Lopes CENDES; L DANSKY; M OGUNI; M H SENI et al. 1993. Epilepsy and pregnancy: twenty years experience. Canadian journal of neurological sciences. Canadá. 20, S20-S20.
  527. Health Sciences Neurology (clinical)
    F CENDES; F ANDERMANN; P GLOOR; A EVANS; T PETERS et al. 1993. Mri volumetric study: insights into the etiology of temporal lobe epilepsy. Canadian journal of neurological sciences. Canadá. 20, S20-S20.
  528. Health Sciences Psychiatry and Mental Health
    Iscia Teresinha Lopes CENDES; E ANDERMANN; D O CONNOR; A SHERWIN; M H SENI et al. 1993. Evidence for changes in cbz pharmacokinetics during pregnancy. Epilepsia. Noruega. 34, 75-75.
  529. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; K SILVER; L SIAVALAS; E ANDERMANN. 1993. Evaluation of neurological development in offspring of epileptic women. Epilepsia. Noruega. 34, 144-144.
  530. Health Sciences Medicine (miscellaneous)
    F CENDES; F ANDERMANN; P GLOOR; Iscia Teresinha Lopes CENDES; E ANDERMANN et al. 1993. Severity of mesial temporal lobe atrophy correlate with history of prolonged febrile convulsions but not with frequency and duration of habitual seizures. Epilepsia. Noruega. 34, 71-71.
  531. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; E ATTIG; F CENDES; J RADVANY et al. 1993. Linkage analysis shows evidence for three different spinocerebellar ataxia loci. Canadian journal of neurological sciences. Canadá. 20, S29-S29.
  532. Health Sciences Medicine (miscellaneous)
    E ANDERMANN; Iscia Teresinha Lopes CENDES; L DANSKY; M OGUNI; M H SENI et al. 1993. Pre-pregnancy counselling and pregnancy monitoring in over three hundred epileptic women. Canadian journal of neurological sciences. Canadá. 20, S149-S149.
  533. Life Sciences Genetics
    S BOSCH; M WAGNER; F GERSTEMBRAND; E ANDERMANN; Iscia Teresinha Lopes CENDES et al. 1993. Spinocerebellar ataxia in a austrian-american family. Canadian journal of neurological sciences. Canadá. 20, S93-S93.
  534. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; E ATTIG; F CENDES; J RADVANY et al. 1993. Clinical and genetic studies in dominantly inherited spinocerebellar ataxias (scas): analyses of clinical and genetic heterogeneity. American journal of human genetics. Estados Unidos. 53, A469-A469.
  535. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; M M GUERREIRO; E A SILVA; J I COCHIUS; E ANDERMANN et al. 1993. Absence of locus heterogeneity in benign familial neonatal convulsions of brazilian origin. Epilepsia. Estados Unidos. 35, 60-61.
  536. Life Sciences Genetics
    J I COCHIUS; Iscia Teresinha Lopes CENDES; S F BERKOVIC; I E SCHEFFER; E ANDERMANN et al. 1993. Linkage analysis in a large family with idiopathic generalized epilepsy: exclusion of candidate regions for epilepsy genes. Epilepsia. Estados Unidos. 35, 64-64.
  537. Health Sciences Rheumatology
    E ANDERMANN; S LEONBERG; S CARPENTER; F SALASPUIG; J FARRER et al. 1993. Autosomal dominant progressive myoclonic epilepsy (pme): strategies: in the diagnosis of kufs'disease. Epilepsia. Estados Unidos. 35, 60-60.
  538. Health Sciences Neurology (clinical)
    A GAMBARDELLA; F CENDES; F ANDERMANN; F DUBEAU; Iscia Teresinha Lopes CENDES et al. 1993. Etiologic; genetic and clinical characteristics of patients with unilateral and with bilateral mesial temporal atrophy. Epilepsia. Estados Unidos. 37, 124-124.
  539. Life Sciences Genetics
    F ANDERMANN; E ANDERMANN; S LEONBERG; S CARPENTER; F SALASPUIG et al. 1993. Autosomal dominant progressive myoclonic epilepsy (pme): evidence for genetic heterogeneity in kufs'disease. American journal of human genetics. Estados Unidos. 34, 144-144.
  540. Health Sciences Medicine (miscellaneous)
    E ANDERMANN; Iscia Teresinha Lopes CENDES; L DANSKY; M OGUNI; M H SENI et al. 1993. Counseling in epileptic women of child bearing age. American journal of human genetics. Estados Unidos. 53, A45-A45.
  541. Health Sciences Neurology (clinical)
    Fernando CENDES; Frederick ANDERMANN; F DUBEAU; P GLOOR; A EVANS et al. 1993. Early childhood prolonged febrile convulsions; atrophy and sclerosis of mesial structures and temporal lobe epilepsy: an mri volumetric study. Neurology (cleveland; ohio). Estados Unidos. 43, (6) 1083-1087.
  542. Health Sciences Neurology (clinical)
    Fernando CENDES; Frederick ANDERMANN; P GLOOR; A EVANS; M Jones GOTMAN et al. 1993. Mri volumetric measurements of amygdala and hippocampus in temporal lobe epilepsy. Neurology (cleveland; ohio). 43, (4) 719-725.
  543. Health Sciences Neurology (clinical)
    F CENDES; F ANDERMANN; F DUBEAU; P GLOOR; A EVANS et al. 1993. Early childhood prolonged febrile convulsions; atrophy and sclerosis of mesial structures and temporal epilepsy: an mri volumetric study. Neurology (cleveland; ohio). Estados Unidos. 43, 1083-1087.
  544. Health Sciences Neurology (clinical)
    F CENDES; F ANDERMANN; P GLOOR; Iscia Teresinha Lopes CENDES; E ANDERMANN et al. 1993. Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures?. Annals of neurology. 34, 795-801.
  545. Health Sciences Medicine (miscellaneous)
    S KANEKO; D BATINO; E ANDERMANN; Y FUKUSHIMA; R KAN et al. 1993. International collaborative study on mechanisms of teratogenesis of antiepileptic drugs (a preliminary report). Anais da 25a rba saberes e práticas antropológicas desafios para o século xxi. 5, 191-199.
  546. Health Sciences Medicine (miscellaneous)
    E ANDERMANN; Iscia Teresinha Lopes CENDES; L DANSKY; F CENDES; M OGUNI et al. 1993. Low dosage folate supplementation before and during pregnancy for women with epilepsy reduces the risk of abnormal pregnancy outcomes. Neurology. Estados Unidos. 43, A300-A300.
  547. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; F CENDES; A SHERWIN; F ANDERMANN. 1992. Interictal scalp eeg during pregnancy in epileptic patients: lack of correlation with changes in seizure frequency and total antiepileptic blood levels. Electroencephalography and clinical neurophysiology. Estados Unidos. 83, 16P-16P.
  548. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; F CENDES; J DONAT; F OOSMAN et al. 1992. Dominant hereditary spinocerebellar ataxia associated with motor neuron disease: a clinical and genetic study in a large saskatchewan kindred. Canadian journal of neurological sciences. Canadá. 19, 279-280.
  549. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; L DANSKY; A SHERWIN; M OGUNI et al. 1992. Anti-epileptic drug levels in pregnant epileptic patients: correlation with changes in seizure frequency. Canadian journal of neurological sciences. Canadá. 19, 266-266.
  550. Health Sciences Medicine (miscellaneous)
    E ANDERMANN; Iscia Teresinha Lopes CENDES; L DANSKY; M OGUNI; F CENDES et al. 1992. Folate supplementation and blood folate levels in pregnant epileptic patients taking anti-epileptic drugs: correlation with outcome of pregnancy. Canadian journal of neurological sciences. Canadá. 19, 250-250.
  551. Health Sciences Neurology (clinical)
    F CENDES; F ANDERMANN; P GLOOR; Iscia Teresinha Lopes CENDES; A OLIVIER et al. 1992. Mesial temporal atrophy: cause or consequence of repeated seizures? evidence from computerized volumetric studies. Canadian journal of neurological sciences. Canadá. 19, 266-267.
  552. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; E ANDERMANN; M SHOKEIR; G A ROULEAU. 1992. Dominant spinocerebellar ataxia in a large saskatchewan kindred: clinical and linkage studies. American journal of human genetics. Canadá. 51, A306-A306.
  553. Health Sciences Neurology (clinical)
    K SILVER; Iscia Teresinha Lopes CENDES; L SIAVALAS; E ANDERMANN. 1992. Risk factors for abnormal neurological development in offspring of epileptic women on anticonvulsant drugs. American journal of human genetics. Estados Unidos. 51, A123-A123.
  554. Health Sciences Medicine (miscellaneous)
    E ANDERMANN; Iscia Teresinha Lopes CENDES; M H SENI. 1992. A prospective study of maternal serum alpha-fetoprotein in epileptic women taking medication during pregnancy: correlation with pregnancy outcome. American journal of human genetics. Estados Unidos. 51, A252-A252.
  555. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; D O CONNOR; A SHERWIN; M H SENI. 1992. Free antiepileptic drug levels during pregnancy: a prospective study. Epilepsia. Estados Unidos. 33, 108-108.
  556. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; E ANDERMANN; F CENDES; L DANSKY; F ANDERMANN. 1992. Risk factors for changes in seizure frequency during pregnancy of epileptic women: a cohort study. Epilepsia. Estados Unidos. 33, 57-57.
  557. Health Sciences Neurology (clinical)
    F CENDES; F ANDERMANN; P GLOOR; Iscia Teresinha Lopes CENDES; E ANDERMANN. 1992. Atrophy of mesial temporal structures in patients with temporal lobe epilepsy (tle): cause or consequence?. Epilepsia. Estados Unidos. 33, 71-71.
  558. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; E ANDERMANN; F GERSTENBRAND; S BOSCH; M WAGNER et al. 1992. Linkage studies in spinocerebellar ataxia (sca): evidence showing that the recently described sca 2 locus is not a private gene. Neurology. Estados Unidos. 43, A358-A359.
  1. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES. 2022. A genética na classificação das epilepsias. In: Proneuro: programa de atualização em neurologia: ciclo3: volume2. Brasil.
  2. Life Sciences Neuroscience (miscellaneous)
    Amorim Rebeca PADRÃO; Iscia Teresinha Lopes CENDES; Da Silva Fernandes Maria JOSÉ. 2020. Chapter 5 - using rna interference for purinoceptor knockdown in vivo. In: Purinergic signaling - methods and protocols - methods in molecular biology. Espanha.
  3. Health Sciences Medicine (miscellaneous)
    Patricia T BOZZA; Sergio D J PENA; Cesar G VICTORA; Helena B NADER; Iscia Teresinha Lopes CENDES et al. 2018. Saúde por inteiro - doenças são apenas uma parte do campo amplo das ciências da saúde. In: Projeto de ciência para o brasil. Brasil.
  4. Health Sciences General Medicine
    Iscia Teresinha Lopes CENDES; Fernando CENDES. 2014. O tratamento em condições especiais. In: Tratamento medicamentoso das epilepsias. Brasil.
  5. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES; Maurer Morelli Claudia V; Fábio ROGÉRIO; Fábio Rossi TORRES; Tiago Campos PEREIRA et al. 2012. Estudos de genética e biologia molecular no âmbito do cinapce: a experiência do mrc da unicamp e centros colaboradores. In: Neurociências e epilepsia - série cinapce. Brasil.
  6. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2009. Determinantes genéticos da cognição e do desenvolvimento cerebral humano. In: Neurologia do desenvolvimento da criança. Brasil.
  7. Life Sciences Genetics
    Iscia Teresinha Lopes CENDES. 2009. Aspectos genéticos. In: Doença de huntington - guia para famílias e profissionais de saúde. Brasil.
  8. Social Sciences & Humanities Psychology (miscellaneous)
    Rejane Scolari Resende PAIVA; Iscia Teresinha Lopes CENDES. 2009. O teste preditivo. In: Doença de huntington. Brasil.
  9. Health Sciences Neurology (clinical)
    Maria Isabel C R MORAIS; Iscia Teresinha Lopes CENDES. 2009. Epilepsias mioclônicas progressivas. In: Condutas em neurologia infantil. Brasil.
  10. Life Sciences Neuroscience (miscellaneous)
    Fábio Rossi TORRES; Daniela Aguiar De Souza KOLS; Simone Sayuri TSUNEDA; Rodrigo SECOLIN; Iara Leda Brandão De Almeida PEREIRA et al. 2008. Malformações do desenvolvimento cortical: estudos genéticos; moleculares e de neuroimagem. In: Neurociências e epilepsia. Brasil.
  11. Health Sciences Medicine (miscellaneous)
    Cláudia V Maurer MORELLI; Cristiane De Souza ROCHA; Romenia Ramos DOMINGUES; Helder TEDESCHI; E OLIVEIRA et al. 2008. Perfil da expressão gênica na epilepsia de lobo temporal mesial familial associada com atrofia hipocampal. In: Neurociências e epilepsia. Brasil.
  12. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2008. Superando limites: a vida com ataxia. In: Superando limites: a vida com ataxia. Brasil.
  13. Health Sciences Neurology (clinical)
    F CENDES; Eliane KOBAYASHI; Iscia Teresinha Lopes CENDES; F ANDERMANN; E ANDERMANN. 2007. Familial temporal lobe epilepsies. In: Epilepsy: a comprehensive textbook; 2e. Estados Unidos.
  14. Health Sciences Neurology (clinical)
    Fernando CENDES; Eliane KOBAYASHI; Iscia Teresinha Lopes CENDES; Frederick ANDERMANN; Eva ANDERMANN. 2006. Familial temporal lobe epilepsies. In: Epilepsy: a comprehensive textbook. Brasil.
  15. Life Sciences Genetics
    Rodrigo SECOLIN; Iscia Teresinha Lopes CENDES. 2006. Estratégias para identificação de genes que predispõem a doenças. In: Genética em oftalmologia: bases moleculares. Brasil.
  16. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2006. Determinantes genéticos da cognição e do desenvolvimento cerebral humano. In: Neurologia do desenvolvimento da criança. Brasil.
  17. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2006. Epilepsia na mulher e gravidez. In: Crises epilépticas e epilepsias ao longo da vida: 100 questões práticas. Brasil.
  18. Health Sciences Neurology (clinical)
    Maria Isabel C R MORAIS; Iscia Teresinha Lopes CENDES. 2006. Epilepsias mioclônicas progressivas. In: Epilepsias generalizadas. Brasil.
  19. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; Patrícia Aline Oliveira Ribeiro De Aguiar ARAÚJO. 2006. Aspectos genéticos das epilepsias generalizadas. In: Epilepsias generalizadas. Brasil.
  20. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; Fernando CENDES. 2004. O tratamento em condições especiais. In: Tratamento medicamentoso das epilepsias. Brasil.
  21. Health Sciences Neurology (clinical)
    Maria Isabel C R MORAIS; Iscia Teresinha Lopes CENDES. 2003. Epilepsias mioclônicas progressivas. In: Condutas em neurologia infantil. Brasil.
  22. Life Sciences Neurology
    José SERRATOSA; Iscia Teresinha Lopes CENDES; Alejandro SCARAMELLI. 2003. Genética y epilepsias. In: Epilepsias: diagnostico y tratamiento. Chile.
  23. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2002. Aspectos genéticos das epilepsias refratárias. In: Epilepsias refratárias. Brasil.
  24. Health Sciences Neurology (clinical)
    Iscia Teresinha Lopes CENDES; P MACIEL; I LOPESCENDES; J SEQUEIROS. 2001. Doença de machado-joseph: avanços recentes e aplicações diagnósticas. In: Manual de medicina fetal. Portugal.
  25. Life Sciences Aging
    Iscia Teresinha Lopes CENDES. 2001. Genética do envelhecimento. In: Maturidade e velhice. Brasil.
  26. Social Sciences & Humanities Psychology (miscellaneous)
    Iscia Teresinha Lopes CENDES; J C C ROCHA; L B JARDIM. 2001. Testes preditivos. In: Projeto diretrizes. Brasil.
  27. Health Sciences Health Professions (miscellaneous)
    Iscia Teresinha Lopes CENDES. 2001. Ataxias hereditárias. In: Tópicos selecionados de neurologia. Brasil.
  28. Health Sciences Neurology (clinical)
    C A M GUERREIRO; M M GUERREIRO; F CENDES; Iscia Teresinha Lopes CENDES. 2000. Epilepsia: considerações gerais. In: Epilepsia. Brasil.
  29. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 2000. Genética e síndromes epilépticas familiares. In: Epilepsia. Brasil.
  30. Life Sciences Endocrinology
    Iscia Teresinha Lopes CENDES; C A M GUERREIRO. 2000. Aspectos reprodutivo endócrinos. In: Epilepsia. Brasil.
  31. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES; F CENDES. 1999. O tratamento em condições especiais. In: Tratamento medicamentoso das epilepsias. Brasil.
  32. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1998. Bases genéticas e moleculares das epilepsias. In: Fundamentos neurobiológicos das epilepsias: aspectos clínicos e cirúrgicos. Brasil.
  33. Life Sciences Neuroscience (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1995. Aspectos genéticos das epilepsias. In: Epilepsia. Brasil.
  34. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES. 1995. Epilepsias mioclônicas progressivas. In: Epilepsia. Brasil.
  35. Health Sciences Medicine (miscellaneous)
    Iscia Teresinha Lopes CENDES. 1993. Aspectos genéticos das epilepsias. In: Epilepsia. Brasil.
  1. Life Sciences Neurology
    Iscia Teresinha Lopes CENDES; C A M GUERREIRO; M M GUERREIRO; F CENDES; I LOPESCENDES. 2000. Epilepsia. Brasil.