Cossette P - Search Results

1

Autosomal dominant juvenile myoclonic epilepsy and GABRA1.

Cossette P, Lortie A, Vanasse M, Saint-Hilaire JM, Rouleau GA. Cossette P, et al. Adv Neurol. 2005;95:255-63. Adv Neurol. 2005. PMID: 15508928 Review. No abstract available.

2

Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.

Meijer IA, Hand CK, Cossette P, Figlewicz DA, Rouleau GA. Meijer IA, et al. Among authors: cossette p. Arch Neurol. 2002 Feb;59(2):281-6. doi: 10.1001/archneur.59.2.281. Arch Neurol. 2002. PMID: 11843700

3

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.

Cossette P, Liu L, Brisebois K, Dong H, Lortie A, Vanasse M, Saint-Hilaire JM, Carmant L, Verner A, Lu WY, Wang YT, Rouleau GA. Cossette P, et al. Nat Genet. 2002 Jun;31(2):184-9. doi: 10.1038/ng885. Epub 2002 May 6. Nat Genet. 2002. PMID: 11992121

4

Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS).

Cossette P, Loukas A, Lafrenière RG, Rochefort D, Harvey-Girard E, Ragsdale DS, Dunn RJ, Rouleau GA. Cossette P, et al. Epilepsy Res. 2003 Feb;53(1-2):107-17. doi: 10.1016/s0920-1211(02)00259-0. Epilepsy Res. 2003. PMID: 12576172

5

Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.

Stumpf E, Masson H, Duquette A, Berthelet F, McNabb J, Lortie A, Lesage J, Montplaisir J, Brais B, Cossette P. Stumpf E, et al. Among authors: cossette p. Arch Neurol. 2003 Sep;60(9):1307-12. doi: 10.1001/archneur.60.9.1307. Arch Neurol. 2003. PMID: 12975300

6

Insulinoma misdiagnosed as intractable epilepsy.

Dion MH, Cossette P, St-Hilaire JM, Rasio E, Nguyen DK. Dion MH, et al. Among authors: cossette p. Neurology. 2004 Apr 27;62(8):1443-5. doi: 10.1212/01.wnl.0000120751.67940.3a. Neurology. 2004. PMID: 15111699 No abstract available.

7

A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.

Meijer IA, Cossette P, Roussel J, Benard M, Toupin S, Rouleau GA. Meijer IA, et al. Among authors: cossette p. Ann Neurol. 2004 Oct;56(4):579-82. doi: 10.1002/ana.20239. Ann Neurol. 2004. PMID: 15455396

8

Clinical significance of isolated hippocampal volume asymmetry in childhood epilepsy.

Major P, Décarie JC, Nadeau A, Diadori P, Lortie A, Nguyen D, Cossette P, Carmant L. Major P, et al. Among authors: cossette p. Neurology. 2004 Oct 26;63(8):1503-6. doi: 10.1212/01.wnl.0000142079.79612.cb. Neurology. 2004. PMID: 15505176

9

Genetic influence on the clinical characteristics and outcome of febrile seizures--a retrospective study.

Birca A, Guy N, Fortier I, Cossette P, Lortie A, Carmant L. Birca A, et al. Among authors: cossette p. Eur J Paediatr Neurol. 2005;9(5):339-45. doi: 10.1016/j.ejpn.2005.03.001. Epub 2005 Jun 23. Eur J Paediatr Neurol. 2005. PMID: 15979359

10

Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy.

Krampfl K, Maljevic S, Cossette P, Ziegler E, Rouleau GA, Lerche H, Bufler J. Krampfl K, et al. Among authors: cossette p. Eur J Neurosci. 2005 Jul;22(1):10-20. doi: 10.1111/j.1460-9568.2005.04168.x. Eur J Neurosci. 2005. PMID: 16029191

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