Brunet D - Search Results

1

A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada.

Valdmanis PN, Brunet D, St-Onge J, Weston L, Rouleau GA, Dupré N. Valdmanis PN, et al. Among authors: brunet d. Neurology. 2006 Dec 26;67(12):2239-42. doi: 10.1212/01.wnl.0000249314.96183.48. Neurology. 2006. PMID: 17190954

2

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

3

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

4

Propofol-related infusion syndrome heralding a mitochondrial disease: case report.

Savard M, Dupré N, Turgeon AF, Desbiens R, Langevin S, Brunet D. Savard M, et al. Among authors: brunet d. Neurology. 2013 Aug 20;81(8):770-1. doi: 10.1212/WNL.0b013e3182a1aa78. Epub 2013 Jul 19. Neurology. 2013. PMID: 23873972 Free PMC article.

5

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

6

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

7

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.

8

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

9

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

10

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.

Leblond CS, Gan-Or Z, Spiegelman D, Laurent SB, Szuto A, Hodgkinson A, Dionne-Laporte A, Provencher P, de Carvalho M, Orrù S, Brunet D, Bouchard JP, Awadalla P, Dupré N, Dion PA, Rouleau GA. Leblond CS, et al. Among authors: brunet d. Neurobiol Aging. 2016 Jan;37:209.e17-209.e21. doi: 10.1016/j.neurobiolaging.2015.09.013. Epub 2015 Sep 28. Neurobiol Aging. 2016. PMID: 26493020

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