Bouchard JP - Search Results

1

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

2

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

3

A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophy.

Mathieu J, Lapointe G, Brassard A, Tremblay C, Brais B, Rouleau GA, Bouchard JP. Mathieu J, et al. Among authors: bouchard jp. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S100-4. doi: 10.1016/s0960-8966(97)00092-8. Neuromuscul Disord. 1997. PMID: 9392026 Clinical Trial.

4

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.

5

Nuclear inclusions in oculopharyngeal muscular dystrophy in Quebec.

Bouchard JP, Gagné F, Tomé FM, Brunet D. Bouchard JP, et al. Can J Neurol Sci. 1989 Nov;16(4):446-50. doi: 10.1017/s0317167100029565. Can J Neurol Sci. 1989. PMID: 2553230

6

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.

Brais B, Bouchard JP, Xie YG, Rochefort DL, Chrétien N, Tomé FM, Lafrenière RG, Rommens JM, Uyama E, Nohira O, Blumen S, Korczyn AD, Heutink P, Mathieu J, Duranceau A, Codère F, Fardeau M, Rouleau GA. Brais B, et al. Among authors: bouchard jp. Nat Genet. 1998 Feb;18(2):164-7. doi: 10.1038/ng0298-164. Nat Genet. 1998. PMID: 9462747

7

Autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Bouchard JP, Richter A, Mathieu J, Brunet D, Hudson TJ, Morgan K, Melançon SB. Bouchard JP, et al. Neuromuscul Disord. 1998 Oct;8(7):474-9. doi: 10.1016/s0960-8966(98)00055-8. Neuromuscul Disord. 1998. PMID: 9829277

8

Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease.

Blumen SC, Brais B, Korczyn AD, Medinsky S, Chapman J, Asherov A, Nisipeanu P, Codère F, Bouchard JP, Fardeau M, Tomé FM, Rouleau GA. Blumen SC, et al. Among authors: bouchard jp. Ann Neurol. 1999 Jul;46(1):115-8. Ann Neurol. 1999. PMID: 10401788

9

A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12.

Jarry J, Rioux MF, Bolduc V, Robitaille Y, Khoury V, Thiffault I, Tétreault M, Loisel L, Bouchard JP, Brais B. Jarry J, et al. Among authors: bouchard jp. Brain. 2007 Feb;130(Pt 2):368-80. doi: 10.1093/brain/awl270. Epub 2006 Sep 28. Brain. 2007. PMID: 17008331

10

The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13.

Brais B, Xie YG, Sanson M, Morgan K, Weissenbach J, Korczyn AD, Blumen SC, Fardeau M, Tomé FM, Bouchard JP, et al. Brais B, et al. Among authors: bouchard jp. Hum Mol Genet. 1995 Mar;4(3):429-34. doi: 10.1093/hmg/4.3.429. Hum Mol Genet. 1995. PMID: 7795598

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