Rouleau G - Search Results

1

Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy.

Gauquelin L, Hartley T, Tarnopolsky M, Dyment DA, Brais B, Geraghty MT, Tétreault M, Ahmed S, Rojas S, Choquet K, Majewski J, Bernier F, Innes AM, Rouleau G, Suchowersky O, Boycott KM, Yoon G. Gauquelin L, et al. Among authors: rouleau g. Mov Disord Clin Pract. 2020 Sep 29;7(8):940-949. doi: 10.1002/mdc3.13086. eCollection 2020 Nov. Mov Disord Clin Pract. 2020. PMID: 33163565 Free PMC article.

2

Oculopharyngeal muscular dystrophy: What's new?

Codère F, Brais B, Rouleau G, Lafontaine E. Codère F, et al. Among authors: rouleau g. Orbit. 2001 Dec;20(4):259-266. doi: 10.1076/orbi.20.4.259.2617. Orbit. 2001. PMID: 12045902

3

Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy.

Abu-Baker A, Messaed C, Laganiere J, Gaspar C, Brais B, Rouleau GA. Abu-Baker A, et al. Hum Mol Genet. 2003 Oct 15;12(20):2609-23. doi: 10.1093/hmg/ddg293. Epub 2003 Aug 27. Hum Mol Genet. 2003. PMID: 12944420

4

HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.

Fan X, Messaed C, Dion P, Laganiere J, Brais B, Karpati G, Rouleau GA. Fan X, et al. Among authors: rouleau ga. Can J Neurol Sci. 2003 Aug;30(3):244-51. doi: 10.1017/s0317167100002675. Can J Neurol Sci. 2003. PMID: 12945950

5

Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophy.

Abu-Baker A, Laganiere S, Fan X, Laganiere J, Brais B, Rouleau GA. Abu-Baker A, et al. Traffic. 2005 Sep;6(9):766-79. doi: 10.1111/j.1600-0854.2005.00315.x. Traffic. 2005. PMID: 16101680 Free article.

6

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.

7

The dynamism of PABPN1 nuclear inclusions during the cell cycle.

Marie-Josée Sasseville A, Caron AW, Bourget L, Klein AF, Dicaire MJ, Rouleau GA, Massie B, Langelier Y, Brais B. Marie-Josée Sasseville A, et al. Neurobiol Dis. 2006 Sep;23(3):621-9. doi: 10.1016/j.nbd.2006.05.015. Epub 2006 Jul 24. Neurobiol Dis. 2006. PMID: 16860991

8

Characterization of a novel SPG3A deletion in a French-Canadian family.

Meijer IA, Dion P, Laurent S, Dupré N, Brais B, Levert A, Puymirat J, Rioux MF, Sylvain M, Zhu PP, Soderblom C, Stadler J, Blackstone C, Rouleau GA. Meijer IA, et al. Ann Neurol. 2007 Jun;61(6):599-603. doi: 10.1002/ana.21114. Ann Neurol. 2007. PMID: 17427918

9

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. Ann Neurol. 2007 Jul;62(1):93-8. doi: 10.1002/ana.21143. Ann Neurol. 2007. PMID: 17503513

10

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. Can J Neurol Sci. 2007 May;34(2):211-4. doi: 10.1017/s0317167100006065. Can J Neurol Sci. 2007. PMID: 17598600

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