Vanasse M - Search Results

1

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: vanasse m. Ann N Y Acad Sci. 1999 Sep 14;883:497-9. Ann N Y Acad Sci. 1999. PMID: 10586283 No abstract available.

2

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: vanasse m. 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.

3

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: vanasse m. Can J Neurol Sci. 1999 Aug;26(3):196-200. doi: 10.1017/s031716710000024x. Can J Neurol Sci. 1999. PMID: 10451742

4

Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion.

Montermini L, Richter A, Morgan K, Justice CM, Julien D, Castellotti B, Mercier J, Poirier J, Capozzoli F, Bouchard JP, Lemieux B, Mathieu J, Vanasse M, Seni MH, Graham G, Andermann F, Andermann E, Melançon SB, Keats BJ, Di Donato S, Pandolfo M. Montermini L, et al. Among authors: vanasse m. Ann Neurol. 1997 May;41(5):675-82. doi: 10.1002/ana.410410518. Ann Neurol. 1997. PMID: 9153531

5

Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families.

Simard LR, Vanasse M, Rochette C, Morgan K, Lemieux B, Melançon SB, Labuda D. Simard LR, et al. Among authors: vanasse m. Genomics. 1992 Sep;14(1):188-90. doi: 10.1016/s0888-7543(05)80305-2. Genomics. 1992. PMID: 1427826

6

Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster.

Gosselin I, Thiffault I, Tétreault M, Chau V, Dicaire MJ, Loisel L, Emond M, Senderek J, Mathieu J, Dupré N, Vanasse M, Puymirat J, Brais B. Gosselin I, et al. Among authors: vanasse m. Neuromuscul Disord. 2008 Jun;18(6):483-92. doi: 10.1016/j.nmd.2008.04.001. Epub 2008 Jun 3. Neuromuscul Disord. 2008. PMID: 18511281

7

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: vanasse m. Brain. 2006 Sep;129(Pt 9):2332-40. doi: 10.1093/brain/awl110. Epub 2006 May 3. Brain. 2006. PMID: 16672289

8

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum.

Dupré N, Howard HC, Mathieu J, Karpati G, Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Dupré N, et al. Among authors: vanasse m. Ann Neurol. 2003 Jul;54(1):9-18. doi: 10.1002/ana.77777. Ann Neurol. 2003. PMID: 12838516 Review.

9

Tremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31.

Bernard G, Thiffault I, Tetreault M, Putorti ML, Bouchard I, Sylvain M, Melançon S, Laframboise R, Langevin P, Bouchard JP, Vanasse M, Vanderver A, Sébire G, Brais B. Bernard G, et al. Among authors: vanasse m. Neurogenetics. 2010 Oct;11(4):457-64. doi: 10.1007/s10048-010-0251-8. Epub 2010 Jul 17. Neurogenetics. 2010. PMID: 20640464 Free PMC article.

10

Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian population.

Simard LR, Prescott G, Rochette C, Morgan K, Lemieux B, Mathieu J, Melançon SB, Vanasse M. Simard LR, et al. Among authors: vanasse m. Hum Mol Genet. 1994 Mar;3(3):459-63. doi: 10.1093/hmg/3.3.459. Hum Mol Genet. 1994. PMID: 8012358

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