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Evidence for existence of a fourth dominantly inherited spinocerebellar ataxia locusLOPES-CENDES, I; ANDERMANN, E; ROULEAU, G. A et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 1, pp 270-274, issn 0888-7543Article

Clinical correlates of autonomic dysfunction in patients with Machado-Joseph diseaseFRANCA, M. C; D'ABREU, A; NUCCI, A et al.Acta neurologica scandinavica. 2010, Vol 121, Num 6, pp 422-425, issn 0001-6314, 4 p.Article

Familial temporal lobe epilepsy : A clinically heterogeneous syndromeCENDES, F; LOPES-CENDES, I; ANDERMANN, E et al.Neurology. 1998, Vol 50, Num 2, pp 554-557, issn 0028-3878Article

Seizure frequency during pregnancy and the puerperiumCOSTA, A. L. C; LOPES-CENDES, I; GUERREIRO, C. A. M et al.International journal of gynaecology and obstetrics. 2005, Vol 88, Num 2, pp 148-149, issn 0020-7292, 2 p.Article

Longitudinal analysis of regional grey matter loss in Huntington disease : effects of the length of the expanded CAG repeatRUOCCO, H. H; BONILHA, L; LI, L. M et al.Journal of neurology, neurosurgery and psychiatry. 2008, Vol 79, Num 2, pp 130-135, issn 0022-3050, 6 p.Article

Mosaicism of the CAG repeat in CNS tissue in relation to age at death in Spinocerebellar ataxia type 1 and Machado-Joseph disease patientsMACIEL, P; LOPES-CENDES, I; KISH, S et al.American journal of human genetics. 1997, Vol 60, Num 4, pp 993-996, issn 0002-9297Article

MRI reveals structural abnormalities in patients with idiopathic generalized epilepsyBETTING, L. E; MORY, S. B; LOPES-CENDES, I et al.Neurology. 2006, Vol 67, Num 5, pp 848-852, issn 0028-3878, 5 p.Article

Genetic linkage studies in familial frontal epilepsy : exclusion of the human chromosome regions homologous to the El-1 mouse locusLOPES-CENDES, I; PHILLIPS, H. A; ROULEAU, G. A et al.Epilepsy research. 1995, Vol 22, Num 3, pp 227-233, issn 0920-1211Article

Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsyCENDES, F; ANDERMANN, F; GLOOR, P et al.Brain. 1994, Vol 117, pp 739-746, issn 0006-8950, 4Article

A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2LOPES-CENDES, I; SCHEFFER, I. E; BERKOVIC, S. F et al.American journal of human genetics. 2000, Vol 66, Num 2, pp 698-701, issn 0002-9297Article

Seizure outcome and hippocampal atrophy in familial mesial temporal lobe epilepsyKOBAYASHI, E; LOPES-CENDES, I; GUERREIRO, C. A. M et al.Neurology. 2001, Vol 56, Num 2, pp 166-172, issn 0028-3878Article

Clinical and genetic heterogeneity in familial temporal lobe epilepsySANTOS, N. F; SOUSA, S. C; KOBAYASHI, E et al.Epilepsia (Copenhagen). 2002, Vol 43, issn 0013-9580, p. 136, SUP5Conference Paper

Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patientsSILVEIRA, I; LOPES-CENDES, I; PINTO-JUNIOR, W et al.Neurology. 1996, Vol 46, Num 1, pp 214-218, issn 0028-3878Article

Linkage disequilibrium analysis in Machado-Joseph disease patients of different ethnic originsGASPAR, C; LOPES-CENDES, I; DESTEFANO, A. L et al.Human genetics. 1996, Vol 98, Num 5, pp 620-624, issn 0340-6717Article

Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesia structures, and temporal lobe epilepsy : an MRI volumetric studyCENDES, F; ANDERMANN, F; PETERS, T et al.Neurology. 1993, Vol 43, Num 6, pp 1083-1087, issn 0028-3878Article

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsyMINASSIAN, B. A; LEE, J. R; JARDIM, L et al.Nature genetics. 1998, Vol 20, Num 2, pp 171-174, issn 1061-4036Article

Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12NECHIPORUK, A; LOPES-CENDES, I; NECHIPORUK, T et al.Neurology. 1996, Vol 46, Num 6, pp 1731-1735, issn 0028-3878Article

Autosomal dominant frontal epilepsy misdiagnosed as a sleep disorderSCHEFFER, I. E; BHATIA, K. P; BERKOVIC, S. F et al.Lancet (British edition). 1994, Vol 343, Num 8896, pp 515-517, issn 0140-6736Article

Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopiaTORRES, F. R; MONTENEGRO, M. A; MARQUES-DE-FARIA, A. P et al.Neurology. 2004, Vol 62, Num 5, pp 799-802, issn 0028-3878, 4 p.Article

Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsyKOBAYASHI, E; D'AGOSTINO, M. D; LOPES-CENDES, I et al.Neurology. 2003, Vol 60, Num 3, pp 405-409, issn 0028-3878, 5 p.Article

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate regionLOPES-CENDES, I; ANDERMANN, E; ATTIG, E et al.American journal of human genetics. 1994, Vol 54, Num 5, pp 774-781, issn 0002-9297Article

Antiepileptic drug response in temporal lobe epilepsy: A clinical and MRI morphometry studyBILEVICIUS, E; YASUDA, C. L; SILVA, M. S et al.Neurology. 2010, Vol 75, Num 19, pp 1695-1701, issn 0028-3878, 7 p.Article

Relationship between environmental factors and gray matter atrophy in refractory MTLEYASUDA, C. L; MORITA, M. E; GUERREIRO, C. A. M et al.Neurology. 2010, Vol 74, Num 13, pp 1062-1068, issn 0028-3878, 7 p.Article

Congenital Bilateral Perisylvian Syndrome : Familial Occurrence, Clinical and Psycholinguistic Aspects Correlated with MRIBRANDAO-ALMEIDA, I. L; HAGE, S. R. V; GUERREIRO, M. M et al.Neuropediatrics. 2008, Vol 39, Num 3, pp 139-145, issn 0174-304X, 7 p.Article

Polyglutamine-containing proteins in schizophreniaJOOBER, R; BENKELFAT, C; ROULEAU, G et al.Molecular psychiatry. 1999, Vol 4, Num 1, pp 53-57, issn 1359-4184Article

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