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M I C R MORAIS; Fernando CENDES; C A M GUERREIRO; L S QUEIROZ; M L CINTRA et al. 2003. Epilepsias mioclônicas progressivas: aspectos clínicos e genéticos. Journal of epilepsy and clinical neurophysiology. Brasil. 9, (2) 115-122.

Luiz E G G BETTING; Susana B MORY; Patricia A O RIBEIRO; L M LI; C A M GUERREIRO et al. 2003. Associated clinical conditions and seizure control in idiopathic generalised epilepsy. Epilepsia. Estados Unidos. 44, (Suppl 8) 158-158.

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.

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.

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.

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.

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.

Eliane KOBAYASHI; Daniela FACCHIN; Carlos Eduardo STEINER; A V A LEONE; Nilma Lúcia Viguetti CAMPOS et al. 2002. Mesial temporal lobe abnormalities in a family with 15q26-qter trisomy. Archives of neurology. Estados Unidos. 59, (9) 1476-1479.

Maria Augusta MONTENEGRO; Marilisa Mantovani GUERREIRO; Iscia LOPESCENDES; Carlos Alberto M GUERREIRO; Li Li MIN 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, (12) 1291-1294.

Eliane KOBAYASHI; Li Li MIN; Iscia LOPESCENDES; 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). Estados Unidos. 59, (12) 1891-1894.

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-.

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; 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-.

Heloisa H RUOCCO; M S SILVA; T L LAURITO; M A VIANA; E M B A QUAGLIATO et al. 2002. Quantificação da atrofia do caudato e putamem por rm volumétrica em pacientes comdoença de huntington. relação entre repetição do cag expandido e idade de início. Arq neuropsiq. Brasil. 60, (Suppl 1) 31-.

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-.

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.

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.

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.

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.

Eliane KOBAYASHI; Fernando CENDES; I LOPESCENDES; C A M GUERREIRO; S C SOUSA et al. 2001. Seizure outcome and hippocampal atrophy in familial mesial temporal lobe epilepsy. Neurology (online). 56, (2) 166-172.

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.

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.

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.

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.

N F SANTOS; S C SOUSA; Eliane KOBAYASHI; Fabio R TORRES; L A SARDINHA et al. 2001. Cinical and genetic heterogeneity in familial temporal lobe epilepsy. Neurology. Estados Unidos. 56, (Suppl 3) A154-A155.

Eliane KOBAYASHI; N F SANTOS; S C SOUSA; Fabio R TORRES; R SECOLIN et al. 2001. Magnetic resonance imaging (mri) abnormalities in familial temporal lobe epilepsy with auditory auras. Epilepsia. Estados Unidos. 42, (Suppl 7) 63-63.

Daniela FACCHIN; Eliane KOBAYASHI; Fernando CENDES; Carlos Eduardo STEINER; A V A LEONE et al. 2000. Epilepsia generalizada secundária em pacientes com 46;xy;der(15)t(15-12)(q26-p13). Brasil.

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.

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

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.

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; Iscia Lopes CENDES; C A M GUERREIRO; B P DAMASCENO; D C HONORATO et al. 2000. Tratamento cirúrgico em pacientes com epilepsia de lobo temporal familiar. Brazilian journal of epilepsy and clin. neurophysiology. Brasil. 6, (2) 91-91.

Eliane KOBAYASHI; D FACCHIN; Fernando CENDES; C E STEINER; Andrea Alessio A LEONE et al. 2000. Epilepsia generalizada secundária em pacientes com trissomia parcial 15 q26-qter. Brazilian journal of epilepsy and clin. neurophysiology. Brasil. 6, (2) 122-122.

Maria Augusta MONTENEGRO; Iscia Lopes CENDES; W FERNANDES; L S FERREIRA; Fernando CENDES. 2000. Disgenesias corticais: contribuição de fatores genéticos e ambientais na sua etiologia. Brazilian journal of epilepsy and clin. neurophysiology. Brasil. 6, (2) 122-122.

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; 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.

Eliane KOBAYASHI; D FACHIN; C E STEINER; Andrea Alessio A LEONE; N L CAMPOS et al. 2000. Epilepsia secundária e deficiência mental relacionada a alterações citogenéticas. Arquivos de neuro psiquiatria. Brasil. 58, (Suppl II) 11-11.

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.

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; 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.

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.

Maria Augusta MONTENEGRO; M M GUERREIRO; Iscia Lopes CENDES; Fernando CENDES. 2000. Bilateral posterior parietal polymicrogyria: a mild form of congenital bilateral perisylvian syndrome?. Epilepsia. Estados Unidos. 41, (Suppl 7) 100-101.

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.

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.

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.

Iscia Lopes CENDES; Fernando CENDES. 1999. O tratamento em condições especiais. In: Tratamento medicamentoso das epilepsias. Brasil.

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; 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.

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; 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.

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.

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.

Eliane KOBAYASHI; S C SOUSA; T C L SILVA; Iscia Lopes CENDES; Fernando CENDES. 1998. Epilepsia de lobo temporal familiar. Brazilian journal of epilepsy and clin. neurophysiology. Brasil. 4, (2) 85-85.

Eliane KOBAYASHI; T C L SILVA; S C SOUSA; A E SCOTONI; C A M GUERREIRO et al. 1998. Epilepsias idiopáticas familiares. Arquivos de neuropsiquiatria. Brasil. 56, (S-1) 25-25.

D AGOSTINO; D ANDERMANN; E XIONG; L LABUDA; M PANDOLFO et al. 1998. Clinical and pedigree analysis in familial temporal lobe epilepsy (tle). Epilepsia. Estados Unidos. 39, (S-6) 177-177.

M D DAOSTINO; E ANDERMANN; S F BERKOVIC; Iscia Lopes CENDES; Fernando CENDES et al. 1998. Familial temporal lobe epilepsy (ftle): clincal characterization and preliminary linkage studies. American journal of human genetics. Estados Unidos. 63, (Suppl) A101-A101.

Iscia Lopes CENDES; Fernando CENDES; E ANDERMANN; Frederick ANDERMANN. 1997. Familial temporal lobe epilepsy: a clinically heterogeneous syndrome. Epilepsia. Estados Unidos. 38, (S8) S200-S200.

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.

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.

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

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 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.

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.

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; 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; 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 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 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 ANDERMANN; E ATTIG; Fernando CENDES; J RADVANY et al. 1993. Clinical and genetic studies in dominantly inherited spinocerebellar ataxias: analyses of clinical and genetic heterogeneity. American journal of human genetics. Estados Unidos. 52, (Suppl) 469-469.

Fernando CENDES; Frederick ANDERMANN; P GLOOR; A EVANS; M Jones GOTMAN et al. 1993. Mri volumetric measurement of amygdala and hippocampus in temporal lobe epilepsy. Neurology (cleveland; ohio). 43, 719-725.

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.

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.

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.

Iscia Lopes CENDES; E ANDERMANN; Fernando CENDES; A L SHERWIN; Frederick ANDERMANN. 1992. Interictal scalp eeg during pregnancy in epileptic patients: lack of correlation with changes in seizure frequency and total antiepileptic blood levels. Eletroencephalograpy and clinical neurophysiology. Estados Unidos. 83, (2) 16P-16P.

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 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.

Mario PEDRAZZOLI; Rodrigo SECOLIN; Luiz Otavio Bastos ESTEVES; D S 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.

Iscia Lopes CENDES; Hélio A G TEIVE; Maria Elisa CALCAGNOTTO; Jaderson Costa Da COSTA; Francisco CARDOSO et al. 1997. Frequency of the differente mutations causing spinocerebellar ataxia (sca1; sca2; mjd/sca3 an drpla) in a large group of brazilian patients. Arquivos de neuro-psiquiatria. Brasil. 55, 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-.

França Marcondes C; Calcagnotto Maria E; Jaderson Costa Da COSTA; Lopes Cendes ISCIA. 2006. Spinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family. Movement disorders. 21, 1051-1053.

Maria Daniela D AGOSTINO; Andrea BERNASCONI; Soma DAS; Alexandre BASTOS; Rosa M VALERIO et al. 2002. Subcortical band heterotopia (sbh) in males: clinical; imaging and genetic findings in comparison with females. Brain. 125, 2507-.

Iscia Lopes CENDES; Hélio A G TEIVE; Maria Elisa CALCAGNOTTO; Jaderson Costa Da COSTA; Francisco CARDOSO et al. 1997. Frequency of the differente mutations causing spinocerebellar ataxia (sca1; sca2; mjd/sca3 an drpla) in a large group of brazilian patients. Arquivos de neuro-psiquiatria. Brasil. 55, 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-.

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.

Laura Maria De Figueiredo Ferreira GUILHOTO; P A O RIBEIRO; L G G BETTING; N F SANTOS; E KOBAYASHI 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-.

Mory Susana BARRETO; Guerreiro Marilisa M; Lopes Cendes ISCIA; Cendes FERNANDO; Guerreiro Carlos A M et al. 2011. Structural abnormalities of the thalamus in juvenile myoclonic epilepsy. Epilepsy & behavior (print). 21, 407-411.

Betting Luiz E; Li Li MIN; Lopes Cendes ISCIA; Guerreiro Marilisa M; Guerreiro Carlos A M et al. 2010. Correlation between quantitative eeg and mri in idiopathic generalized epilepsy. Human brain mapping. NA-NA.

Heloísa H RUOCCO; Leonardo BONILHA; Li Li MIN; Iscia LOPESCENDES; Fernando 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.

Maria Augusta MONTENEGRO; Fernando CENDE; I LOPESCENDES; Carlos Alberto GUERREIRO; Li Li MIN et al. 2007. The clinical spectrum of malformations of cortical development. Arquivos de neuro-psiquiatria. 65, 196-201.

Heloísa H RUOCCO; Íscia LOPESCENDES; Li Li MIN; Fernando CENDES. 2007. Evidence of thalamic dysfunction in huntington disease by proton magnetic resonance spectroscopy. Movement disorders. 22, 2052-2056.

Heloísa H RUOCCO; Íscia LOPESCENDES; Marilisa Mantovani GUERREIRO; Li Li MIN; C A M GUERREIRO. 2006. Clinical presentation of juvenile huntington disease. Arquivos de neuro-psiquiatria. Brasil. 64, (1) 5-9.

L E BETTING; S B MORY; Li Li MIN; Íscia LOPESCENDES; Marilisa Mantovani GUERREIRO et al. 2006. Mri volumetry shows increased anterior thalamic volumes in patients with absence seizures. Epilepsy & behavior. Estados Unidos. 8, (3) 575-578.

L E BETTING; S B MORY; Íscia LOPESCENDES; Li Li MIN; Marilisa Mantovani GUERREIRO et al. 2006. Eeg features in idiopathic generalized epilepsy: clues to diagnosis. Epilepsia. 47, (3) 523-528.

Maria Augusta MONTENEGRO; D KINAY; Fernando CENDES; Andrea BERNASCONI; Neda BERNASCONI et al. 2006. Patterns of hippocampal abnormalities in malformations of cortical development. Journal of neurology; neurosurgery and psychiatry. Grã-Bretanha. 77, (3) 367-371.

Luiz Eduardo BETTING; Susana B MORY; Iscia LOPESCENDES; Li Li MIN; Carlos A Mantovani GUERREIRO et al. 2006. Mri reveals structural abnormalities in patients with idiopathic generalized epilepsy. Neurology (cleveland; ohio). 12, 848-852.

Heloísa H RUOCCO; Iscia LOPESCENDES; Li Li MIN; M Santos SILVA; Fernando 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, 1129-1136.

Luiz Eduardo BETTING; Mory Susana BARRETO; Li Li MIN; Lopes Cendes ISCIA; Guerreiro Marilisa M et al. 2006. Voxel-based morphometry in patients with idiopathic generalized epilepsies. Neuroimage. 32, 498-502.

Bi L BRANDÃOALMEIDA; S R V HAGE; C A GUIMARÃES; N F SANTOS; E P M OLIVEIRA et al. 2004. Polimicrogiria perisylviana bilateral congênita: aspectos clínicos; eletrencefalográficos; neuroradiológicos; psicolingüísticos e genéticos. Journal of epilepsy and clinical neurophysiology. Brasil. 10, (1) 7-12.

A C COAN; E KOBAYASHI; I LOPESCENDES; Li Li MIN; F CENDES. 2004. Abnormalities of hippocampal signal intensity in patients with familial mesial temporal lobe epilepsy. Brazilian journal of medical and biological research. Brasil. 37, (6) 827-832.

E KOBAYASHI; M D D AGOSTINO; I LOPESCENDES; S F BERKOVIC; Li Li MIN et al. 2003. Hippocampal atrophy and t2-weighted signal changes in familial mesial temporal lobe epilepsy. Neurology (cleveland; ohio). Brasil. 60, (3) 405-409.

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