Prévost C - Search Results

1

Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population.

Howard HC, Dubé MP, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Howard HC, et al. Among authors: prevost c. Eur J Hum Genet. 2002 Jul;10(7):406-12. doi: 10.1038/sj.ejhg.5200815. Eur J Hum Genet. 2002. PMID: 12107814

2

The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.

Howard HC, Mount DB, Rochefort D, Byun N, Dupré N, Lu J, Fan X, Song L, Rivière JB, Prévost C, Horst J, Simonati A, Lemcke B, Welch R, England R, Zhan FQ, Mercado A, Siesser WB, George AL Jr, McDonald MP, Bouchard JP, Mathieu J, Delpire E, Rouleau GA. Howard HC, et al. Among authors: prevost c. Nat Genet. 2002 Nov;32(3):384-92. doi: 10.1038/ng1002. Epub 2002 Oct 7. Nat Genet. 2002. PMID: 12368912

3

The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

Casaubon LK, Melanson M, Lopes-Cendes I, Marineau C, Andermann E, Andermann F, Weissenbach J, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Casaubon LK, et al. Among authors: prevost c. Am J Hum Genet. 1996 Jan;58(1):28-34. Am J Hum Genet. 1996. PMID: 8554065 Free PMC article.

4

[Motor and sensory neuropathies with or without agenesis of the corpus callosum: a radiological study of 64 cases].

Mathieu J, Bédard F, Prévost C, Langevin P. Mathieu J, et al. Among authors: prevost c. Can J Neurol Sci. 1990 May;17(2):103-8. Can J Neurol Sci. 1990. PMID: 2357646 French.

5

Rapid detection of the sacsin mutations causing autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Mercier J, Prévost C, Engert JC, Bouchard JP, Mathieu J, Richter A. Mercier J, et al. Among authors: prevost c. Genet Test. 2001 Fall;5(3):255-9. doi: 10.1089/10906570152742326. Genet Test. 2001. PMID: 11788093

6

Diversity of ARSACS mutations in French-Canadians.

Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, Dupré N, Prévost C, Bouchard JP, Mathieu J, Brais B. Thiffault I, et al. Among authors: prevost c. Can J Neurol Sci. 2013 Jan;40(1):61-6. doi: 10.1017/s0317167100012968. Can J Neurol Sci. 2013. PMID: 23250129

7

Epidemiological surveillance of myotonic dystrophy type 1: a 25-year population-based study.

Mathieu J, Prévost C. Mathieu J, et al. Among authors: prevost c. Neuromuscul Disord. 2012 Nov;22(11):974-9. doi: 10.1016/j.nmd.2012.05.017. Epub 2012 Aug 1. Neuromuscul Disord. 2012. PMID: 22858159

8

Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markers.

Thibault MC, Mathieu J, Moorjani S, Lescault A, Prévost C, Gaudet D, Morissette J, Laberge C. Thibault MC, et al. Among authors: prevost c. Can J Neurol Sci. 1989 Feb;16(1):134-40. doi: 10.1017/s0317167100028687. Can J Neurol Sci. 1989. PMID: 2924208

9

Sibship stability of genotype and phenotype in myotonic dystrophy.

Brisson D, Tremblay M, Prévost C, Laberge C, Puymirat J, Mathieu J. Brisson D, et al. Among authors: prevost c. Clin Genet. 2002 Sep;62(3):220-5. doi: 10.1034/j.1399-0004.2002.620306.x. Clin Genet. 2002. PMID: 12220437

10

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada).

Mathieu J, De Braekeleer M, Prévost C. Mathieu J, et al. Among authors: prevost c. Neurology. 1990 May;40(5):839-42. doi: 10.1212/wnl.40.5.839. Neurology. 1990. PMID: 2330114

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