Intracerebroventricular infusion of monoclonal antibody or its derived Fab fragment against misfolded forms of SOD1 mutant delays mortality in a mouse model of ALSGROS-LOUIS, Francois; SOUCY, Geneviève; LARIVIERE, Roxanne et al.Journal of neurochemistry. 2010, Vol 113, Num 5, pp 1188-1199, issn 0022-3042, 12 p.Article

Une nouvelle forme d'ataxie récessive causée par des mutations du gène SYNE-1 = Mutations in SYNE-I lead to a newly discovered form of autosomal recessive cerebellar ataxiaDUPRE, Nicolas; BOUCHARD, Jean-Pierre; GROS-LOUIS, Francois et al.MS. Médecine sciences. 2007, Vol 23, Num 3, pp 261-262, issn 0767-0974, 2 p.Article

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1DUPRE, Nicolas; GROS-LOUIS, Francois; CHRESTIAN, Nicolas et al.Annals of neurology. 2007, Vol 62, Num 1, pp 93-98, issn 0364-5134, 6 p.Article

Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafishGROS-LOUIS, Francois; KRIZ, Jasna; JULIEN, Jean-Pierre et al.Human molecular genetics (Print). 2008, Vol 17, Num 17, pp 2691-2702, issn 0964-6906, 12 p.Article

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosisHAND, Collette K; DEVON, Rebecca S; GROS-LOUIS, Francois et al.Archives of neurology (Chicago). 2003, Vol 60, Num 12, pp 1768-1771, issn 0003-9942, 4 p.Article

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxiaGROS-LOUIS, Francois; DUPRE, Nicolas; DION, Patrick et al.Nature genetics. 2007, Vol 39, Num 1, pp 80-85, issn 1061-4036, 6 p.Article