Lopes-Cendes I - Search Results

1

Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder.

Scheffer IE, Bhatia KP, Lopes-Cendes I, Fish DR, Marsden CD, Andermann E, Andermann F, Desbiens R, Keene D, Cendes F, et al. Scheffer IE, et al. Brain. 1995 Feb;118 ( Pt 1):61-73. doi: 10.1093/brain/118.1.61. Brain. 1995. PMID: 7895015

2

Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder.

Scheffer IE, Bhatia KP, Lopes-Cendes I, Fish DR, Marsden CD, Andermann F, Andermann E, Desbiens R, Cendes F, Manson JI, et al. Scheffer IE, et al. Lancet. 1994 Feb 26;343(8896):515-7. doi: 10.1016/s0140-6736(94)91463-x. Lancet. 1994. PMID: 7906762 Review.

3

Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy.

Cendes F, Andermann F, Gloor P, Gambardella A, Lopes-Cendes I, Watson C, Evans A, Carpenter S, Olivier A. Cendes F, et al. Brain. 1994 Aug;117 ( Pt 4):739-46. doi: 10.1093/brain/117.4.739. Brain. 1994. PMID: 7922461

4

Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus.

Lopes-Cendes I, Andermann E, Rouleau GA. Lopes-Cendes I, et al. Genomics. 1994 May 1;21(1):270-4. doi: 10.1006/geno.1994.1257. Genomics. 1994. PMID: 8088802

5

Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric study.

Cendes F, Andermann F, Dubeau F, Gloor P, Evans A, Jones-Gotman M, Olivier A, Andermann E, Robitaille Y, Lopes-Cendes I, et al. Cendes F, et al. Neurology. 1993 Jun;43(6):1083-7. doi: 10.1212/wnl.43.6.1083. Neurology. 1993. PMID: 8170546

6

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

Lopes-Cendes I, Andermann E, Attig E, Cendes F, Bosch S, Wagner M, Gerstenbrand F, Andermann F, Rouleau GA. Lopes-Cendes I, et al. Am J Hum Genet. 1994 May;54(5):774-81. Am J Hum Genet. 1994. PMID: 8178818 Free PMC article.

7

Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures?

Cendes F, Andermann F, Gloor P, Lopes-Cendes I, Andermann E, Melanson D, Jones-Gotman M, Robitaille Y, Evans A, Peters T. Cendes F, et al. Ann Neurol. 1993 Dec;34(6):795-801. doi: 10.1002/ana.410340607. Ann Neurol. 1993. PMID: 8250528

8

MRI volumetric measurement of amygdala and hippocampus in temporal lobe epilepsy.

Cendes F, Andermann F, Gloor P, Evans A, Jones-Gotman M, Watson C, Melanson D, Olivier A, Peters T, Lopes-Cendes I, et al. Cendes F, et al. Neurology. 1993 Apr;43(4):719-25. doi: 10.1212/wnl.43.4.719. Neurology. 1993. PMID: 8469329

9

The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

Casaubon LK, Melanson M, Lopes-Cendes I, Marineau C, Andermann E, Andermann F, Weissenbach J, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Casaubon LK, et al. Am J Hum Genet. 1996 Jan;58(1):28-34. Am J Hum Genet. 1996. PMID: 8554065 Free PMC article.

10

Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.

Silveira I, Lopes-Cendes I, Kish S, Maciel P, Gaspar C, Coutinho P, Botez MI, Teive H, Arruda W, Steiner CE, Pinto-Júnior W, Maciel JA, Jerin S, Sack G, Andermann E, Sudarsky L, Rosenberg R, MacLeod P, Chitayat D, Babul R, Sequeiros J, Rouleau GA. Silveira I, et al. Neurology. 1996 Jan;46(1):214-8. doi: 10.1212/wnl.46.1.214. Neurology. 1996. PMID: 8559378

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