Brunet D - Search Results

1

Phenotypic Manifestations in French-Canadian Population with Charcot-Marie-Tooth Disease Type 1A Associated with 17p11.2 Duplication.

Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J. Dupré N, et al. Among authors: brunet d. Ann N Y Acad Sci. 1999 Oct;883(1):497-499. doi: 10.1111/j.1749-6632.1999.tb08620.x. Ann N Y Acad Sci. 1999. PMID: 29086976 No abstract available.

2

Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplication.

Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J. Dupré N, et al. Among authors: brunet d. Can J Neurol Sci. 1999 Aug;26(3):196-200. doi: 10.1017/s031716710000024x. Can J Neurol Sci. 1999. PMID: 10451742

3

Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication.

Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J. Dupré N, et al. Among authors: brunet d. Ann N Y Acad Sci. 1999 Sep 14;883:497-9. Ann N Y Acad Sci. 1999. PMID: 10586283 No abstract available.

4

Adrenomyeloneuropathy: report of a new mutation in a French Canadian female.

Dionne A, Brunet D, McCampbell A, Dupré N. Dionne A, et al. Among authors: brunet d. Can J Neurol Sci. 2005 May;32(2):261-3. doi: 10.1017/s0317167100004091. Can J Neurol Sci. 2005. PMID: 16018167

5

A novel mutation in a large French-Canadian family with LGMD1B.

Chrestian N, Valdmanis PN, Echahidi N, Brunet D, Bouchard JP, Gould P, Rouleau GA, Champagne J, Dupré N. Chrestian N, et al. Among authors: brunet d. Can J Neurol Sci. 2008 Jul;35(3):331-4. doi: 10.1017/s031716710000891x. Can J Neurol Sci. 2008. PMID: 18714801

6

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.

Dupré N, Gros-Louis F, Chrestian N, Verreault S, Brunet D, de Verteuil D, Brais B, Bouchard JP, Rouleau GA. Dupré N, et al. Among authors: brunet d. Ann Neurol. 2007 Jul;62(1):93-8. doi: 10.1002/ana.21143. Ann Neurol. 2007. PMID: 17503513

7

Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians.

Dupré N, Chrestian N, Bouchard JP, Rossignol E, Brunet D, Sternberg D, Brais B, Mathieu J, Puymirat J. Dupré N, et al. Among authors: brunet d. Neuromuscul Disord. 2009 May;19(5):330-4. doi: 10.1016/j.nmd.2008.01.007. Epub 2008 Mar 11. Neuromuscul Disord. 2009. PMID: 18337100

8

Nuclear inclusions in oculopharyngeal muscular dystrophy in Quebec.

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

9

C-5 radiculopathy as a manifestation of giant cell arteritis.

Rivest D, Brunet D, Desbiens R, Bouchard JP. Rivest D, et al. Among authors: brunet d. Neurology. 1995 Jun;45(6):1222-4. doi: 10.1212/wnl.45.6.1222-a. Neurology. 1995. PMID: 7783897 No abstract available.

10

Recent studies on oculopharyngeal muscular dystrophy in Québec.

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

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