Rouleau GA - Search Results

1

The genetic landscape of infantile spasms.

Michaud JL, Lachance M, Hamdan FF, Carmant L, Lortie A, Diadori P, Major P, Meijer IA, Lemyre E, Cossette P, Mefford HC, Rouleau GA, Rossignol E. Michaud JL, et al. Among authors: rouleau ga. Hum Mol Genet. 2014 Sep 15;23(18):4846-58. doi: 10.1093/hmg/ddu199. Epub 2014 Apr 29. Hum Mol Genet. 2014. PMID: 24781210

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: rouleau ga. 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. Among authors: rouleau ga. 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. Among authors: rouleau ga. Epilepsy Res. 2003 Feb;53(1-2):107-17. doi: 10.1016/s0920-1211(02)00259-0. Epilepsy Res. 2003. PMID: 12576172

5

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: rouleau ga. Ann Neurol. 2004 Oct;56(4):579-82. doi: 10.1002/ana.20239. Ann Neurol. 2004. PMID: 15455396

6

Autosomal dominant juvenile myoclonic epilepsy and GABRA1.

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

7

Sacred disease secrets revealed: the genetics of human epilepsy.

Turnbull J, Lohi H, Kearney JA, Rouleau GA, Delgado-Escueta AV, Meisler MH, Cossette P, Minassian BA. Turnbull J, et al. Among authors: rouleau ga. Hum Mol Genet. 2005 Sep 1;14(17):2491-500. doi: 10.1093/hmg/ddi250. Epub 2005 Jul 27. Hum Mol Genet. 2005. Corrected and republished in: Hum Mol Genet. 2005 Oct 15;14 Spec No. 2:2491-2500. PMID: 16049035 Corrected and republished. Review.

8

A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors.

Duan QL, Nikpoor B, Dube MP, Molinaro G, Meijer IA, Dion P, Rochefort D, Saint-Onge J, Flury L, Brown NJ, Gainer JV, Rouleau JL, Agostoni A, Cugno M, Simon P, Clavel P, Potier J, Wehbe B, Benarbia S, Marc-Aurele J, Chanard J, Foroud T, Adam A, Rouleau GA. Duan QL, et al. Among authors: rouleau ga, rouleau jl. Am J Hum Genet. 2005 Oct;77(4):617-26. doi: 10.1086/496899. Epub 2005 Sep 1. Am J Hum Genet. 2005. PMID: 16175507 Free PMC article.

9

Sacred disease secrets revealed: the genetics of human epilepsy.

Turnbull J, Lohi H, Kearney JA, Rouleau GA, Delgado-Escueta AV, Meisler MH, Cossette P, Minassian BA. Turnbull J, et al. Among authors: rouleau ga. Hum Mol Genet. 2005 Oct 15;14 Spec No. 2:2491-2500. Hum Mol Genet. 2005. PMID: 16278970 Review.

10

Monogenic epilepsies in humans: molecular mechanisms and relevance for the study of intractable epilepsy.

Cossette P, Rouleau GA. Cossette P, et al. Among authors: rouleau ga. Adv Neurol. 2006;97:381-8. Adv Neurol. 2006. PMID: 16383149 Review. No abstract available.

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