Bouchard JP - Search Results

1

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.

2

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

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

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

6

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

7

Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene.

Brais B, Bouchard JP, Gosselin F, Xie YG, Fardeau M, Tomé FM, Rouleau GA. Brais B, et al. Among authors: bouchard jp. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S70-4. doi: 10.1016/s0960-8966(97)00086-2. Neuromuscul Disord. 1997. PMID: 9392020

8

Diversity of ARSACS mutations in French-Canadians.

Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, Dupré N, Prévost C, Bouchard JP, Mathieu J, Brais B. Thiffault I, et al. Among authors: bouchard jp. Can J Neurol Sci. 2013 Jan;40(1):61-6. doi: 10.1017/s0317167100012968. Can J Neurol Sci. 2013. PMID: 23250129

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

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

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