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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.

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M I C R MORAIS; F ROSSI; M M GUERREIRO; Fernando CENDES; Iscia Lopes CENDES. 2003. Protocolo clínico e molecular para avaliação de pacientes com epilepsia miôclonica progressiva. Brasil.

Patricia A O RIBEIRO; V D B PASCOAL; Luiz E G G BETTING; N F SANTOS; R SECOLIN et al. 2003. Estudos de ligação e associação do locus 6p21 em epilepsias generalizadas idiopáticas. Brasil.

Eliane KOBAYASHI; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2003. Epilepsia de lobo temporal: síndrome ou grupo de síndromes?. Brazilian journal of epilepsy and clinical neurophysiology. Brasil. 9, 41-47.

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.

Fabio R TORRES; A P M FARIA; Maria Augusta MONTENEGRO; M M GUERREIRO; Fernando CENDES et al. 2003. A new missense mutation in a patient with classical lissencephaly. Epilepsia. Estados Unidos. 44, (Suppl 9) 70-71.

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.

R SECOLIN; N F SANTOS; Eliane KOBAYASHI; Fabio R TORRES; L A SARDINHA et al. 2003. Progressos nos estudos de ligação genética em famílias brasileiras com epilepsia do lobo temporal com sintomas auditivos. Brasil.

N F SANTOS; R SECOLIN; Fabio R TORRES; Eliane KOBAYASHI; L A F SARDINHA et al. 2003. Relationship between lgi1 gene mutations; mri abnormalities and clinical status in familial temporal lobe epilepsy with auditory auras. Epilepsia. Estados Unidos. 44, (Suppl 9) 243-243.

Fabio R TORRES; Maria Augusta MONTENEGRO; M C S RODRIGUES; A M PIOVESANA; J C LLERENA et al. 2003. Estudo molecular em uma amostra de pacientes com desordens do desenvolvimento cortical. Brasil.

Fabio R TORRES; Maria Augusta MONTENEGRO; M M GUERREIRO; Fernando CENDES; Iscia Lopes CENDES. 2003. Fln1 mutations in patients with atypical periventricular nodular heterotopia. Neurology. Estados Unidos. 60, (Suppl 1) A279-.

Iscia LOPESCENDES; Fernando CENDES. 2003. O tratamento em condições especiais. In: O tratamento medicamentoso das epilepsias. Brasil.

N F SANTOS; Eliane KOBAYASHI; Fabio R TORRES; R SECCOLIN; L A C SARDINHA et al. 2003. Familial temporal lobe epilepsy with auditory auras: clinical and genetic heterogeneity. Neurology. Estados Unidos. 60, (Suppl 1) A277-.

Luiz E G G BETTING; Patricia A O RIBEIRO; Susana B MORY; L M LI; C A M GUERREIRO et al. 2003. Fatores associados ao desencadeamento de crises em epilepsia generalizada idiopática. Brasil.

Gisele C R CASELATO; Eliane KOBAYASHI; L BONILHA; Gabriela CASTELLANO; A H RIGAS et al. 2003. Análise de textura hipocampal em pacientes com epilepsia de lobo temporal mesial familiar. Brasil.

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.

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.

N F SANTOS; Eliane KOBAYASHI; Fabio R TORRES; R SECOLIN; L A C SARDINHA et al. 2003. Evidência de heterogeneidade clínica e genética para epilepsia do lobo temporal familial com sintomas auditivos. Brasil.

Fabio R TORRES; M C S RODRIGUES; Maria Augusta MONTENEGRO; A M S G PIOVESANA; M M GUERREIRO et al. 2003. Searching for mutations in the emx2 gene in a large sample of patients with schizencephaly. Epilepsia. Estados Unidos. 44, (Suppl 9) 72-72.

I ALMEIDA; Iscia Lopes CENDES; M M GUERREIRO; N SANTOS; C GUIMARÃES et al. 2003. Clinical features and mri findings associated with familial congenital bilateral perisylvian syndrome. Epilepsia. Estados Unidos. 44, (Suppl 8) 90-90.

Andrea Alessio A LEONE; Fernando CENDES; Eliane KOBAYASHI; B P DAMASCENO; Iscia Lopes CENDES. 2002. Relevância da atrofia hipocampal e frequência de crises no déficit de memória em pacientes com epilepsia de lobo temporal familial. Arquivos brasileiros de neuropsiquiatria. Brasil. 60, (Suppl 1) 41-.

Eliane KOBAYASHI; M D D AGOSTINO; Iscia Lopes CENDES; E ANDERMANN; F DUBEAU et al. 2002. Outcome of surgical treatment in patients with familial mesial temporal lobe epilepsy. Neurology. Estados Unidos. 58, (Suppl 3) A95-.

Maria Augusta MONTENEGRO; L M LI; M M GUERREIRO; C A M GUERREIRO; Fernando CENDES. 2002. Patterns of hippocampal abnormalities in malformations of cortical development. Brazilian journal of epilepsy and clin. neurophysiology. Brasil. 8, (2) 109-.

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.

Maria Augusta MONTENEGRO; M M GUERREIRO; Iscia Lopes CENDES; C A M GUERREIRO; L M LI et al. 2002. Family history of epilepsy antecipates seizure onset in focal cortical dysplasia. Neurology. Estados Unidos. 58, (Suppl 3) A123-.

Eliane KOBAYASHI; Andrea Alessio A LEONE; B P DAMASCENO; Iscia Lopes CENDES; Fernando CENDES. 2002. Neuropsychological evaluation in patients with familial mesial temporal lobe epilepsy. Neurology. Estados Unidos. 58, (Suppl 3) A122-.

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.

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.

Maria Augusta MONTENEGRO; M M GUERREIRO; I LOPESCENDES; C A M 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. 77, (12) 1291-1294.

M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; C A M GUERREIRO; Fernando CENDES. 2002. Interrelationship of genetics and prenatal injury in the genesis of malformations of cortical development. Archives of neurology (chicago). 59, 1147-1153.

Kobayashi E; Iscia Teresinha Lopes CENDES; Li M LI; Fernando 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.

N F SANTOS; S C SOUSA; Eliane KOBAYASHI; Fabio R TORRES; L A SARDINHA et al. 2001. Searching for genes predisposing to idiopathic partial epilepsy syndromes. Brasil.

Maria Augusta MONTENEGRO; M M GUERREIRO; Iscia Lopes CENDES; C A M GUERREIRO; Fernando CENDES. 2001. Relevância dos fatôres genéticos e pré-natais nas diferentes formas de malformações do desenvolvimento cortical. Brasil.

Eliane KOBAYASHI; Frederick ANDERMANN; L M LI; Iscia Lopes CENDES; E ANDERMANN et al. 2001. Volumetric studies in familial mesial temporal lobe epilepsy. Neurology. Estados Unidos. 56, (Suppl 3) A153-A153.

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.

Maria Augusta MONTENEGRO; M M GUERREIRO; Iscia Lopes CENDES; C A M GUERREIRO; Fernando CENDES. 2001. Variable severity of epilepsy in different types of malformation of cortical development. Epilepsia. Estados Unidos. 42, (Suppl 2) 15-15.

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). Brasil.

N F SANTOS; S C SOUSA; Eliane KOBAYASHI; Fabio R TORRES; L A SARDINHA et al. 2001. Evidence of linkage between one family with lateral temporal lobe epilepsy and chromossome 10q. Epilepsia. Estados Unidos. 42, (Suppl 2) 79-79.

M A MONTENEGRO; M M GUERREIRO; Iscia Teresinha Lopes CENDES; Fernando CENDES. 2001. Bilateral posterior parietal polymicrogyria: a mild form of congenital bilateral perisylvian syndrome ?. Epilepsia (copenhagen). 42, 845-849.

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.

Elba C S C ETCHEBEHERE; Fernando CENDES; I Lopes CENDES; J A PEREIRA; Mariana Da Cunha Lopes De 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.

Maria Augusta MONTENEGRO; M M GUERREIRO; Iscia Lopes CENDES; C A M GUERREIRO; Fernando CENDES. 2001. Relevance of genetic and prenatal events in different forms of malformations of cortical development. Neurology. Estados Unidos. 56, (Suppl 3) A135-A135.

Elba Camargo S C ETCHEBEHERE; Fernando CENDES; Iscia 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, (Suppl II) 96-96.

Maria Augusta MONTENEGRO; C A M GUERREIRO; Fernando CENDES; Iscia Lopes CENDES. 2000. Malformations of cortical development: contribution of genetic and prenatal events to its etiology. Estados Unidos.

Elba Camargo S C ETCHEBEHERE; Fernando CENDES; Iscia Lopes CENDES; C D RAMOS; A O SANTOS et al. 2000. Brain spect and magnetic resonance imaging in machado-joseph's disease. The journal of nuclear medicine. Estados Unidos. 41, (Suppl) 223P-223P.

Eliane KOBAYASHI; Fernando CENDES; S C SOUSA; C A M GUERREIRO; Iscia Lopes CENDES. 2000. Familial temporal lobe epilepsy with hippocampal atrophy is not linkec to chromossome 10q. Epilepsia. Estados Unidos. 41, (Suppl 7) 73-73.

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.

S C SOUSA; Eliane KOBAYASHI; C A M GUERREIRO; Fernando CENDES; Iscia Lopes CENDES. 2000. Exclusão de ligação entre 18 loci candidatos para epilepsia em famílias com epilepsia de lobo temporal mesial. Arquivos de neuro psiquiatria. Brasil. 58, (Suppl II) 12-12.

Maria Augusta MONTENEGRO; Iscia Lopes CENDES; Fernando CENDES. 2000. Fatores de risco para a ocorrência de polimicrogiria parietal posterior bilateral. Arquivos de neuro psiquiatria. Brasil. 58, (Supp II) 100-100.

S C SOUSA; Eliane KOBAYASHI; M M GUERREIRO; C A M GUERREIRO; Fernando CENDES et al. 2000. Estudo de ligação genética em epilepsia de lobo temporal mesial. Genetics and molecular biology. Brasil. 23, (Suppl 3) 292-293.

Ana Carolina COAN; Eliane KOBAYASHI; Iscia Lopes CENDES; Fernando CENDES. 2000. Alteração de sinal hipocampal em pacientes com epilepsia de lobo temporal familiar. Arquivos de neuro psiquiatria. Brasil. 58, (Suppl II) 10-10.

Eliane KOBAYASHI; D FACCHIN; Fernando CENDES; C E STEINER; Andrea Alessio A LEONE et al. 2000. Secondary generalized epilepsy in patients with karyotype 46; xy; der (15) t (15- 12) (q26- p13). Chile.

Maria Augusta MONTENEGRO; Iscia Lopes CENDES; W FERNANDES; L S FERREIRA; Fernando CENDES. 2000. Fatores genéticos e ambientais na etiologia das disgenesias corticais. Chile.

D M CASTRO; M I C R MORAIS; D FACCHIN; L S FERREIRA; Maria Augusta MONTENEGRO et al. 2000. Estudo de freqüênica de mutações de ponto no mtdna em um grupo de pacientes com suspeita clínica de doença mitocondrial. Genetics and molecular biology. Brasil. 23, (Suppl 3) 292-293.

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.

S C SOUSA; Eliane KOBAYASHI; Fernando CENDES; Iscia Lopes CENDES. 2000. Familial mesial temporal lobe epilepsy (tle) do not mat to chromossome (ch) 10q. Chile.

Eliane KOBAYASHI; S C SOUSA; Iscia Lopes CENDES; C A M GUERREIRO; Fernando CENDES. 2000. Epilepsia de lobo temporal familiar associada a atrofia hipocampal. Arquivos de neuro psiquiatria. Brasil. 58, (Suppl II) 11-11.

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.

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.

Eliane KOBAYASHI; Iscia Lopes CENDES; C A M GUERREIRO; Fernando CENDES. 1999. Eletroencefalograma e ressonância magnética em pacientes com epilepsia de lobo temporal familiar. Arquivos de neuro psiquiatria. Brasil. 57, (Suppl 2) 13-13.

Iscia Lopes CENDES; Eliane KOBAYASHI; S C SOUSA; T C L SILVA; A E SCOTONI et al. 1999. Familial temporal lobe epilepsy: clinical and genetic studies. Neurology. Estados Unidos. 52, (Suppl 2) A546-A546.

Eliane KOBAYASHI; Fernando CENDES; C A M GUERREIRO; Iscia Lopes CENDES. 1999. Mri abnormalities in familial temporal lobe epilepsy. Neurology. Estados Unidos. 52, (Suppl 2) A545-A545.

Elba C S C ETCHEBEHERE; F CENDES; I CENDES; F PEREIRA; Mariana C L LIMA et al. 1999. Spect cerebral na doença de machado-joseph. Argentina.

Eliane KOBAYASHI; Iscia 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, (Suppl 2) 266-266.

S C SOUSA; Eliane KOBAYASHI; C A M GUERREIRO; Fernando CENDES; Iscia Lopes CENDES. 1999. Estudos de ligação em epilepsia de lobo temporal familiar. Genetics and molecular biology. Brasil. 22, (Suppl) 222-222.

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-.

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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-.

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-.

Fernando CENDES; Iscia LOPESCENDES; Frederick ANDERMANN; Lopes Cendes I; E ANDERMANN. 1998. Familial temporal lobe epilepsy: a clinically heterogeneous syndrome. Neurology (cleveland; ohio). 50, 554-557.

Iscia Lopes CENDES; F ARRUDA; Fernando CENDES; L DANSKY; 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, (Sup) A127-A127.

Iscia Lopes CENDES; E ANDERMANN; F ARRUDA; Fernando CENDES; L 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, (S4) 148-148.

I LOPESCENDES; H A PHILIPS; I E SCHEFFER; J C MULLEY; R DESBIENS 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, (3) 227-233.

I LOPESCENDES; J C MULLEY; E ANDERMANN; I E SCHEFFER; S F 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 journal of human genetics. Estados Unidos. 35, A350-A350.

Fernando CENDES; Frederick ANDERMANN; P GLOOR; A GAMBARDELLA; I LOPESCENDES et al. 1994. Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy. Brain (london. print). 117, (Pt 4) 739-746.

I E SCHEFFER; K BHADIA; Iscia Lopes CENDES; D R FISH; C D MARSDEN et al. 1994. Autosomal dominant frontal lobe epilepsy. Estados Unidos.

Iscia Teresinha Lopes CENDES; E ANDERMANN; E ATTIG; Fernando 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.

Iscia Lopes CENDES; E ANDERMANN; E ATIG; Fernando CENDES; J RADVANY et al. 1993. Linkage analysis shows evidence for three different spinocerebellar ataxia loci. The canadian journal of neurological sciences. Canadá. 20, (Suppl 4) S29-S29.

Iscia Lopes CENDES; E ATIG; Fernando CENDES; M I BOTEZ; G A ROULEAU. 1993. Locus heterogeneity in french-canadian families with autossomal dominant spinocerebellar ataxia. The canadian journal of neurological sciences. Canadá. 20, (Suppl 2) S21-S21.

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.

Fernando CENDES; Frederick ANDERMANN; P GLOOR; Iscia 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. Estados Unidos. 34, (Suppl 2) 71-71.

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.

Fernando CENDES; Frederick ANDERMANN; P GLOOR; I LOPESCENDES; 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, (6) 795-801.

Fernando CENDES; Frederick ANDERMANN; P GLOOR; A EVANS; T PETERS et al. 1993. Mri volumetric study: insights into the etiology of temporal lobe epilepsy. The canadian journal of neurological sciences. Canadá. 20, (Suppl 2) S20-S20.

Iscia Lopes CENDES; E ANDERMANN; Fernando CENDES; J DONAT; F COSMAN et al. 1992. Dominant hereditary spinocerebelar 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.

Fernando CENDES; Frederick ANDERMANN; Iscia Lopes CENDES; A EVANS; T PETERS. 1992. Atrophy of mesial temporal structures in patients with temporal lobe epilepsy (tle): cause or consequence?. Epilepsia. Estados Unidos. 33, (Suppl 3) 71-71.

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.

Iscia Lopes CENDES; E ANDERMANN; L DANSKY; A L SHERWIN; M OGUNI et al. 1992. Anti-epileptic drug levels in pregnant epileptic patients: correlation with changes in seizure frequency. The canadian journal of neurological sciences. Canadá. 19, 266-266.

Iscia Lopes CENDES; E ANDERMANN; Fernando CENDES; L DANSKY; Frederick ANDERMANN. 1992. Risk factors for changes in seizure frequency during pregnancy of epileptic women: a cohort study. Epilepsia. Estados Unidos. 33, (Suppl 3) 57-57.

E ANDERMANN; Iscia Lopes CENDES; L DANSKY; M OGUNI; Fernando CENDES et al. 1992. Folate supplementation and blood folate levels in pregnant epileptic patients taking anti-epileptic drugs: correlation with the outcome of pregnancy. The canadian journal of neurological sciences. Canadá. 19, 250-250.

Mario Pedrazzoli NETO; R SECOLIN; L O B ESTEVES; Danyella Silva PEREIRA; Bruna Del Vechio KOIKE et al. 2010. Interactions of polymorphisms in different clock genes associated with circadian phenotypes in humans. Genetics and molecular biology (impresso). 33, 627-632.

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.

I L CENDES; H G A TEIVE; M E CALCAGNOTTO; Jaderson Costa 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 (impresso). 55, (3B) 519-529.

Iscia Lopes CENDES; Helio G A TEIVE; Francisco CARDOSO; Erika M VIANA; Maria Elisa CALCAGNOTTO et al. 1997. Molecular characteristics of machado-joseph disease mutation in 25 newly described brazilian families. Brazilian journal of genetics (impresso). 20, 00-.

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Iscia Lopes CENDES; Helio G A TEIVE; Francisco CARDOSO; Erika M VIANA; Maria Elisa CALCAGNOTTO et al. 1997. Molecular characteristics of machado-joseph disease mutation in 25 newly described brazilian families. Brazilian journal of genetics (impresso). 20, 00-.

I L CENDES; H G A TEIVE; M E CALCAGNOTTO; Jaderson Costa 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 (impresso). 55, (3B) 519-529.

Mcg RODRIGUES; Fr TORRES; Alg MARIANTE; C BARBOSA; R ZLOT et al. 2004. Ausência de mutações no gene homeobox emx2 em 33 pacientes portadores de esquizencefalia. Brasil.

Patricia A O RIBEIRO; Luiz E G G BETTING; N F SANTOS; Susana B MORY; L FLORE et al. 2003. The relevance of gabra1 gene mutations in juvenile myoclonic epilepsy and other forms of idiopathic generalized epilepsy. Neurology. Estados Unidos. 60, (Suppl 1) A92-.

Hélio A G TEIVE; R P MUNOZ; Walter Olescho ARRUDA; Iscia Lopes CENDES; Salmo RASKIN et al. 2012. Spinocerebellar ataxias: genotype-phenotype correlations in 104 brazilian families. Clinics (usp. impresso). 67, 443-449.

H TEIVE; W ARRUDA; S RASKIN; Lineu Cesar WERNECK. 2005. Genotype-phenotype correlation in 100 families with spinocerebelar ataxias. Parkinsonism related disorders. Canadá. 11, 204-205.

H A G TEIVE; W O ARRUDA; S RASKIN; I L CENDES; Lineu Cesar WERNECK. 2004. Correlação genotípica-fenotípica em 100 famílias com ataxias espinocerebelares. O dendrito. Brasil. 10, (2) 34-35.

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