Vanasse M - Search Results

1

Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.

Roddier K, Thomas T, Marleau G, Gagnon AM, Dicaire MJ, St-Denis A, Gosselin I, Sarrazin AM, Larbrisseau A, Lambert M, Vanasse M, Gaudet D, Rouleau GA, Brais B. Roddier K, et al. Among authors: vanasse m. Neurology. 2005 May 24;64(10):1762-7. doi: 10.1212/01.WNL.0000161849.29944.43. Neurology. 2005. PMID: 15911806

2

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

3

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

4

A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21.

Tétreault M, Duquette A, Thiffault I, Bherer C, Jarry J, Loisel L, Banwell B, D'Anjou G, Mathieu J, Robitaille Y, Vanasse M, Brais B. Tétreault M, et al. Among authors: vanasse m. Brain. 2006 Aug;129(Pt 8):2077-84. doi: 10.1093/brain/awl146. Epub 2006 Jun 7. Brain. 2006. PMID: 16760198

5

Autosomal dominant juvenile myoclonic epilepsy and GABRA1.

Cossette P, Lortie A, Vanasse M, Saint-Hilaire JM, Rouleau GA. Cossette P, et al. Among authors: vanasse m. Adv Neurol. 2005;95:255-63. Adv Neurol. 2005. PMID: 15508928 Review. No abstract available.

6

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.

7

Toxic reactions with valproic acid therapy.

Vanasse M, David P, Geoffroy G, Larbrisseau A. Vanasse M, et al. Neurology. 1981 May;31(5):644. doi: 10.1212/wnl.31.5.644-a. Neurology. 1981. PMID: 6785664 No abstract available.

8

Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation.

Debray FG, Lambert M, Lortie A, Vanasse M, Mitchell GA. Debray FG, et al. Among authors: vanasse m. Am J Med Genet A. 2007 Sep 1;143A(17):2046-51. doi: 10.1002/ajmg.a.31880. Am J Med Genet A. 2007. PMID: 17663470 Review.

9

Myelination Delay and Allan-Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 Gene.

La Piana R, Vanasse M, Brais B, Bernard G. La Piana R, et al. Among authors: vanasse m. J Child Neurol. 2015 Sep;30(10):1371-4. doi: 10.1177/0883073814555189. Epub 2014 Nov 7. J Child Neurol. 2015. PMID: 25380603

10

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.

Cossette P, Liu L, Brisebois K, Dong H, Lortie A, Vanasse M, Saint-Hilaire JM, Carmant L, Verner A, Lu WY, Wang YT, Rouleau GA. Cossette P, et al. Among authors: vanasse m. Nat Genet. 2002 Jun;31(2):184-9. doi: 10.1038/ng885. Epub 2002 May 6. Nat Genet. 2002. PMID: 11992121

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

92 results

Search Page

Filters