Bouchard JP - Search Results

1

Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden.

Valdmanis PN, Kabashi E, Dyck A, Hince P, Lee J, Dion P, D'Amour M, Souchon F, Bouchard JP, Salachas F, Meininger V, Andersen PM, Camu W, Dupré N, Rouleau GA. Valdmanis PN, et al. Among authors: bouchard jp. Neurology. 2008 Aug 12;71(7):514-20. doi: 10.1212/01.wnl.0000324997.21272.0c. Neurology. 2008. PMID: 18695162

2

Mutations in FUS cause FALS and SALS in French and French Canadian populations.

Belzil VV, Valdmanis PN, Dion PA, Daoud H, Kabashi E, Noreau A, Gauthier J; S2D team; Hince P, Desjarlais A, Bouchard JP, Lacomblez L, Salachas F, Pradat PF, Camu W, Meininger V, Dupré N, Rouleau GA. Belzil VV, et al. Among authors: bouchard jp. Neurology. 2009 Oct 13;73(15):1176-9. doi: 10.1212/WNL.0b013e3181bbfeef. Epub 2009 Sep 9. Neurology. 2009. PMID: 19741216 Free PMC article.

3

Oculopharyngeal muscular dystrophy.

Brais B, Rouleau GA, Bouchard JP, Fardeau M, Tomé FM. Brais B, et al. Among authors: bouchard jp. Semin Neurol. 1999;19(1):59-66. doi: 10.1055/s-2008-1040826. Semin Neurol. 1999. PMID: 10711989 Review.

4

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.

Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B. Thiffault I, et al. Among authors: bouchard jp. Brain. 2006 Sep;129(Pt 9):2332-40. doi: 10.1093/brain/awl110. Epub 2006 May 3. Brain. 2006. PMID: 16672289

5

Recent studies on oculopharyngeal muscular dystrophy in Québec.

Bouchard JP, Brais B, Brunet D, Gould PV, Rouleau GA. Bouchard JP, et al. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S22-9. doi: 10.1016/s0960-8966(97)00077-1. Neuromuscul Disord. 1997. PMID: 9392011

6

A founder mutation in French-Canadian families with X-linked hereditary neuropathy.

Dupré N, Cossette L, Hand CK, Bouchard JP, Rouleau GA, Puymirat J. Dupré N, et al. Among authors: bouchard jp. Can J Neurol Sci. 2001 Feb;28(1):51-5. doi: 10.1017/s0317167100052550. Can J Neurol Sci. 2001. PMID: 11252295

7

Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene.

Blumen SC, Korczyn AD, Lavoie H, Medynski S, Chapman J, Asherov A, Nisipeanu P, Inzelberg R, Carasso RL, Bouchard JP, Tomé FM, Rouleau GA, Brais B. Blumen SC, et al. Among authors: bouchard jp. Neurology. 2000 Nov 14;55(9):1267-70. doi: 10.1212/wnl.55.9.1267. Neurology. 2000. PMID: 11087766

8

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. Among authors: bouchard jp. Am J Hum Genet. 1996 Jan;58(1):28-34. Am J Hum Genet. 1996. PMID: 8554065 Free PMC article.

9

[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada].

Dupré N, Chrestian N, Thiffault I, Brais B, Rouleau GA, Bouchard JP. Dupré N, et al. Among authors: bouchard jp. Rev Neurol (Paris). 2008 Jan;164(1):12-21. doi: 10.1016/j.neurol.2007.08.006. Epub 2008 Jan 25. Rev Neurol (Paris). 2008. PMID: 18342054 Review. French.

10

K-Cl cotransport in red blood cells from patients with KCC3 isoform mutants.

Lauf PK, Adragna NC, Dupre N, Bouchard JP, Rouleau GA. Lauf PK, et al. Among authors: bouchard jp. Biochem Cell Biol. 2006 Dec;84(6):1034-44. doi: 10.1139/o06-203. Biochem Cell Biol. 2006. PMID: 17215889

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