Gros-Louis F - Search Results

1

Characterization of the phenotype with cognitive impairment and protein mislocalization in SCA34.

Beaudin M, Sellami L, Martel C, Touzel-Deschênes L, Houle G, Martineau L, Lacroix K, Lavallée A, Chrestian N, Rouleau GA, Gros-Louis F, Laforce R Jr, Dupré N. Beaudin M, et al. Neurol Genet. 2020 Feb 20;6(2):e403. doi: 10.1212/NXG.0000000000000403. eCollection 2020 Apr. Neurol Genet. 2020. PMID: 32211516 Free PMC article.

2

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.

Hand CK, Khoris J, Salachas F, Gros-Louis F, Lopes AA, Mayeux-Portas V, Brewer CG, Brown RH Jr, Meininger V, Camu W, Rouleau GA. Hand CK, et al. Am J Hum Genet. 2002 Jan;70(1):251-6. doi: 10.1086/337945. Epub 2001 Nov 9. Am J Hum Genet. 2002. PMID: 11706389 Free PMC article.

3

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.

Hand CK, Devon RS, Gros-Louis F, Rochefort D, Khoris J, Meininger V, Bouchard JP, Camu W, Hayden MR, Rouleau GA. Hand CK, et al. Arch Neurol. 2003 Dec;60(12):1768-71. doi: 10.1001/archneur.60.12.1768. Arch Neurol. 2003. PMID: 14676054

4

A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1.

Valdmanis PN, Simões Lopes AA, Gros-Louis F, Stewart JD, Rouleau GA, Dupré N. Valdmanis PN, et al. J Med Genet. 2004 Aug;41(8):634-9. doi: 10.1136/jmg.2004.019711. J Med Genet. 2004. PMID: 15286160 Free PMC article. No abstract available.

5

A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.

Gros-Louis F, Larivière R, Gowing G, Laurent S, Camu W, Bouchard JP, Meininger V, Rouleau GA, Julien JP. Gros-Louis F, et al. J Biol Chem. 2004 Oct 29;279(44):45951-6. doi: 10.1074/jbc.M408139200. Epub 2004 Aug 17. J Biol Chem. 2004. PMID: 15322088 Free article.

6

Alsin is partially associated with centrosome in human cells.

Millecamps S, Gentil BJ, Gros-Louis F, Rouleau G, Julien JP. Millecamps S, et al. Biochim Biophys Acta. 2005 Aug 15;1745(1):84-100. doi: 10.1016/j.bbamcr.2004.12.008. Epub 2005 Jan 19. Biochim Biophys Acta. 2005. PMID: 16085057 Free article.

7

Genetics of familial and sporadic amyotrophic lateral sclerosis.

Gros-Louis F, Gaspar C, Rouleau GA. Gros-Louis F, et al. Biochim Biophys Acta. 2006 Nov-Dec;1762(11-12):956-72. doi: 10.1016/j.bbadis.2006.01.004. Epub 2006 Feb 10. Biochim Biophys Acta. 2006. PMID: 16503123 Free article. Review.

8

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

9

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. Nat Genet. 2007 Jan;39(1):80-5. doi: 10.1038/ng1927. Epub 2006 Dec 10. Nat Genet. 2007. PMID: 17159980

10

[Mutations in SYNE-1 lead to a newly discovered form of autosomal recessive cerebellar ataxia].

Dupré N, Bouchard JP, Gros-Louis F, Rouleau GA. Dupré N, et al. Med Sci (Paris). 2007 Mar;23(3):261-2. doi: 10.1051/medsci/2007233261. Med Sci (Paris). 2007. PMID: 17349286 Free article. French. No abstract available.

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