Dupré N - Search Results

1

Assessing non-Mendelian inheritance in inherited axonopathies.

Bis-Brewer DM, Gan-Or Z, Sleiman P; Inherited Neuropathy Consortium; Hakonarson H, Fazal S, Courel S, Cintra V, Tao F, Estiar MA, Tarnopolsky M, Boycott KM, Yoon G, Suchowersky O, Dupré N, Cheng A, Lloyd TE, Rouleau G, Schüle R, Züchner S. Bis-Brewer DM, et al. Among authors: dupre n. Genet Med. 2020 Dec;22(12):2114-2119. doi: 10.1038/s41436-020-0924-0. Epub 2020 Aug 3. Genet Med. 2020. PMID: 32741968 Free PMC article.

2

A founder mutation in French-Canadian families with X-linked hereditary neuropathy.

Dupré N, Cossette L, Hand CK, Bouchard JP, Rouleau GA, Puymirat J. Dupré N, et al. Can J Neurol Sci. 2001 Feb;28(1):51-5. doi: 10.1017/s0317167100052550. Can J Neurol Sci. 2001. PMID: 11252295

3

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. Ann Neurol. 2003 Jul;54(1):9-18. doi: 10.1002/ana.77777. Ann Neurol. 2003. PMID: 12838516 Review.

4

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population.

Dupré N, Bouchard JP, Brais B, Rouleau GA. Dupré N, et al. Can J Neurol Sci. 2006 May;33(2):149-57. doi: 10.1017/s031716710000490x. Can J Neurol Sci. 2006. PMID: 16736723 Review.

5

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.

Gros-Louis F, Dupré N, Dion P, Fox MA, Laurent S, Verreault S, Sanes JR, Bouchard JP, Rouleau GA. Gros-Louis F, et al. Among authors: dupre n. Nat Genet. 2007 Jan;39(1):80-5. doi: 10.1038/ng1927. Epub 2006 Dec 10. Nat Genet. 2007. PMID: 17159980

6

Autosomal dominant primary lateral sclerosis.

Dupré N, Valdmanis PN, Bouchard JP, Rouleau GA. Dupré N, et al. Neurology. 2007 Apr 3;68(14):1156-7. doi: 10.1212/01.wnl.0000258678.58808.86. Neurology. 2007. PMID: 17404201 No abstract available.

7

SPG4 founder effect in French Canadians with hereditary spastic paraplegia.

Meijer IA, Dupré N, Brais B, Cossette P, St-Onge J, Rioux MF, Benard M, Rouleau GA. Meijer IA, et al. Among authors: dupre n. Can J Neurol Sci. 2007 May;34(2):211-4. doi: 10.1017/s0317167100006065. Can J Neurol Sci. 2007. PMID: 17598600

8

A locus for primary lateral sclerosis on chromosome 4ptel-4p16.1.

Valdmanis PN, Dupré N, Rouleau GA. Valdmanis PN, et al. Among authors: dupre n. Arch Neurol. 2008 Mar;65(3):383-6. doi: 10.1001/archneur.65.3.383. Arch Neurol. 2008. PMID: 18332252

9

[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada].

Dupré N, Chrestian N, Thiffault I, Brais B, Rouleau GA, Bouchard JP. Dupré N, et al. Rev Neurol (Paris). 2008 Jan;164(1):12-21. doi: 10.1016/j.neurol.2007.08.006. Epub 2008 Jan 25. Rev Neurol (Paris). 2008. PMID: 18342054 Review. French.

10

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.

Belzil VV, St-Onge J, Daoud H, Desjarlais A, Bouchard JP, Dupré N, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: dupre n. J Hum Genet. 2011 Mar;56(3):247-9. doi: 10.1038/jhg.2010.162. Epub 2010 Dec 16. J Hum Genet. 2011. PMID: 21160488

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