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william camu
william camu
chu montpellier
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Year
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
E Kabashi, PN Valdmanis, P Dion, D Spiegelman, BJ McConkey, ...
Nature genetics 40 (5), 572-574, 2008
17832008
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ...
Nature genetics 45 (11), 1353-1360, 2013
13232013
Siponimod versus placebo in secondary progressive multiple sclerosis (EXPAND): a double-blind, randomised, phase 3 study
L Kappos, A Bar-Or, BAC Cree, RJ Fox, G Giovannoni, R Gold, ...
The Lancet 391 (10127), 1263-1273, 2018
9382018
Neurotrophins promote motor neuron survival and are present in embryonic limb bud
CE Henderson, W Camu, C Mettling, A Gouin, K Poulsen, M Karihaloo, ...
Nature 363 (6426), 266-270, 1993
7781993
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5762018
TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1
KK McDonald, A Aulas, L Destroismaisons, S Pickles, E Beleac, W Camu, ...
Human molecular genetics 20 (7), 1400-1410, 2011
4462011
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
L Benajiba, I Le Ber, A Camuzat, M Lacoste, C Thomas‐Anterion, ...
Annals of neurology 65 (4), 470-473, 2009
3562009
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
S Millecamps, F Salachas, C Cazeneuve, P Gordon, B Bricka, A Camuzat, ...
Journal of medical genetics 47 (8), 554-560, 2010
3452010
Effect of natalizumab on disease progression in secondary progressive multiple sclerosis (ASCEND): a phase 3, randomised, double-blind, placebo-controlled trial with an open …
R Kapoor, PR Ho, N Campbell, I Chang, A Deykin, F Forrestal, N Lucas, ...
The Lancet Neurology 17 (5), 405-415, 2018
3252018
A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis
F Gros-Louis, R Larivière, G Gowing, S Laurent, W Camu, JP Bouchard, ...
Journal of Biological Chemistry 279 (44), 45951-45956, 2004
2672004
Neuromyelitis optica in France: a multicenter study of 125 patients
N Collongues, R Marignier, H Zephir, C Papeix, F Blanc, C Ritleng, ...
Neurology 74 (9), 736-742, 2010
2572010
A major determinant for binding and aminoacylation of tRNAAla in cytoplasmic alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease
P Latour, C Thauvin-Robinet, C Baudelet-Méry, P Soichot, V Cusin, ...
The American Journal of Human Genetics 86 (1), 77-82, 2010
2512010
Purification of embryonic rat motoneurons by panning on a monoclonal antibody to the low-affinity NGF receptor
W Camu, CE Henderson
Journal of neuroscience methods 44 (1), 59-70, 1992
2391992
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
H Daoud, PN Valdmanis, E Kabashi, P Dion, N Dupre, W Camu, ...
Journal of medical genetics 46 (2), 112-114, 2009
2322009
A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q
CK Hand, J Khoris, F Salachas, F Gros-Louis, AAS Lopes, ...
The American Journal of Human Genetics 70 (1), 251-256, 2002
2192002
Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes
S Millecamps, S Boillée, I Le Ber, D Seilhean, E Teyssou, M Giraudeau, ...
Journal of medical genetics 49 (4), 258-263, 2012
2162012
Recessive Amyotrophic Lateral Sclerosis Families with the D90A SOD1 Mutation Share a Common Founder: Evidence for a Linked Protective Factor
A Al-Chalabi, PM Andersen, B Chioza, C Shaw, PC Sham, W Robberecht, ...
Human molecular genetics 7 (13), 2045-2050, 1998
2011998
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study
J Gil, B Funalot, A Verschueren, V Danel‐Brunaud, W Camu, ...
European journal of neurology 15 (11), 1245-1251, 2008
1962008
Mutations in FUS cause FALS and SALS in French and French Canadian populations
VV Belzil, PN Valdmanis, PA Dion, H Daoud, E Kabashi, A Noreau, ...
Neurology 73 (15), 1176-1179, 2009
1782009
High metabolic level in patients with familial amyotrophic lateral sclerosis
B Funalot, JC Desport, F Sturtz, W Camu, P Couratier
Amyotrophic Lateral Sclerosis 10 (2), 113-117, 2009
1672009
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