Rouleau GA - Search Results

1

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.

Hand CK, Devon RS, Gros-Louis F, Rochefort D, Khoris J, Meininger V, Bouchard JP, Camu W, Hayden MR, Rouleau GA. Hand CK, et al. Among authors: rouleau ga. Arch Neurol. 2003 Dec;60(12):1768-71. doi: 10.1001/archneur.60.12.1768. Arch Neurol. 2003. PMID: 14676054

2

Superoxide dismutase activity in lymphoblastoid cells from motor neurone disease/amyotrophic lateral sclerosis (MND/ALS) patients.

Garofalo O, Figlewicz DA, Thomas SM, Butler R, Lebuis L, Rouleau G, Meininger V, Leigh PN. Garofalo O, et al. J Neurol Sci. 1995 May;129 Suppl:90-2. doi: 10.1016/0022-510x(95)00073-b. J Neurol Sci. 1995. PMID: 7595631 Free article.

3

Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor.

Al-Chalabi A, Andersen PM, Chioza B, Shaw C, Sham PC, Robberecht W, Matthijs G, Camu W, Marklund SL, Forsgren L, Rouleau G, Laing NG, Hurse PV, Siddique T, Leigh PN, Powell JF. Al-Chalabi A, et al. Hum Mol Genet. 1998 Dec;7(13):2045-50. doi: 10.1093/hmg/7.13.2045. Hum Mol Genet. 1998. PMID: 9817920

4

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.

Hand CK, Khoris J, Salachas F, Gros-Louis F, Lopes AA, Mayeux-Portas V, Brewer CG, Brown RH Jr, Meininger V, Camu W, Rouleau GA. Hand CK, et al. Among authors: rouleau ga. Am J Hum Genet. 2002 Jan;70(1):251-6. doi: 10.1086/337945. Epub 2001 Nov 9. Am J Hum Genet. 2002. PMID: 11706389 Free PMC article.

5

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

6

Familial amyotrophic lateral sclerosis.

Hand CK, Rouleau GA. Hand CK, et al. Among authors: rouleau ga. Muscle Nerve. 2002 Feb;25(2):135-59. doi: 10.1002/mus.10001. Muscle Nerve. 2002. PMID: 11870681 Review.

7

Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population.

Howard HC, Dubé MP, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Howard HC, et al. Among authors: rouleau ga. Eur J Hum Genet. 2002 Jul;10(7):406-12. doi: 10.1038/sj.ejhg.5200815. Eur J Hum Genet. 2002. PMID: 12107814

8

The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.

Howard HC, Mount DB, Rochefort D, Byun N, Dupré N, Lu J, Fan X, Song L, Rivière JB, Prévost C, Horst J, Simonati A, Lemcke B, Welch R, England R, Zhan FQ, Mercado A, Siesser WB, George AL Jr, McDonald MP, Bouchard JP, Mathieu J, Delpire E, Rouleau GA. Howard HC, et al. Among authors: rouleau ga. Nat Genet. 2002 Nov;32(3):384-92. doi: 10.1038/ng1002. Epub 2002 Oct 7. Nat Genet. 2002. PMID: 12368912

9

An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred.

Gros-Louis F, Meijer IA, Hand CK, Dubé MP, MacGregor DL, Seni MH, Devon RS, Hayden MR, Andermann F, Andermann E, Rouleau GA. Gros-Louis F, et al. Among authors: rouleau ga. Ann Neurol. 2003 Jan;53(1):144-5. doi: 10.1002/ana.10422. Ann Neurol. 2003. PMID: 12509863 No abstract available.

10

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

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