Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("GROS-LOUIS, Francois")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 8 of 8

  • Page / 1

Export

Selection :

  • and

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

Resequencing of 29 Candidate Genes in Patients With Familial and Sporadic Amyotrophic Lateral SclerosisDAOUD, Hussein; VALDMANIS, Paul N; DION, Patrick A et al.Archives of neurology (Chicago). 2011, Vol 68, Num 5, pp 587-593, issn 0003-9942, 7 p.Article

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18qHAND, Collette K; KHORIS, Jawad; SALACHAS, Francois et al.American journal of human genetics. 2002, Vol 70, Num 1, pp 251-256, issn 0002-9297Article

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

  • Page / 1