Rouleau GA - Search Results

1

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

2

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

3

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

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

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.

Dupré N, Verlaan DJ, Hand CK, Laurent SB, Turecki G, Davenport WJ, Acciarri N, Dichgans J, Ohkuma A, Siegel AM, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Can J Neurol Sci. 2003 May;30(2):122-8. doi: 10.1017/s0317167100053385. Can J Neurol Sci. 2003. PMID: 12774951

6

[Severe neuropathy with agenesis of the corpus callosum].

Howard HC, Dupré N, Mathieu J, Bouchard JP, Rouleau GA. Howard HC, et al. Among authors: rouleau ga. Med Sci (Paris). 2003 Apr;19(4):414-6. doi: 10.1051/medsci/2003194414. Med Sci (Paris). 2003. PMID: 12836214 Free article. French. No abstract available.

7

Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia.

Toulouse A, Rochefort D, Roussel J, Joober R, Rouleau GA. Toulouse A, et al. Among authors: rouleau ga. Genomics. 2003 Aug;82(2):162-71. doi: 10.1016/s0888-7543(03)00101-0. Genomics. 2003. PMID: 12837267

8

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum.

Dupré N, Howard HC, Mathieu J, Karpati G, Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Ann Neurol. 2003 Jul;54(1):9-18. doi: 10.1002/ana.77777. Ann Neurol. 2003. PMID: 12838516 Review.

9

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

10

Mutational analysis of neurotensin in familial restless legs syndrome.

Desautels A, Turecki G, Xiong L, Rochefort D, Montplaisir J, Rouleau GA. Desautels A, et al. Among authors: rouleau ga. Mov Disord. 2004 Jan;19(1):90-4. doi: 10.1002/mds.10617. Mov Disord. 2004. PMID: 14743366

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