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Annals of Neurology|May 19, 1998
Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron diseaseB Moulard, F Salachas, B Chassande, et al.Journal of the Neurological Sciences|August 17, 1999
Genetics of familial ALS and consequences for diagnosis. French ALS Research GroupW Camu, J Khoris, B Moulard, et al.Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|June 14, 2002
Long-term safety of riluzole in amyotrophic lateral sclerosisL Lacomblez, G Bensimon, P N Leigh, et al.Neurology|January 13, 2006
Pentoxifylline in ALS: a double-blind, randomized, multicenter, placebo-controlled trialV Meininger, B Asselain, P Guillet, et al.Neurology|February 11, 2012
Genotype-phenotype relationship in 2 SMA III patients with novel mutations in the Tudor domainM J Fraidakis, S Drunat, T Maisonobe, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 26, 1998
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosisY Boukaftane, J Khoris, B Moulard, et al.American Journal of Respiratory and Critical Care Medicine|August 1, 1997
Influence of neck muscles on mouth pressure response to cervical magnetic stimulationV Attali, S Mehiri, C Straus, et al.Neurology|December 1, 1996
A confirmatory dose-ranging study of riluzole in ALS. ALS/Riluzole Study Group-IIL Lacomblez, G Bensimon, P N Leigh, et al.Revue Neurologique|May 5, 2000
[What's new in primary lateral sclerosis?]N Le Forestier, T Maisonobe, L Spelle, et al.American Journal of Respiratory and Critical Care Medicine|March 11, 2000
Sleep disorders and diaphragmatic function in patients with amyotrophic lateral sclerosisI Arnulf, T Similowski, F Salachas, et al.Pageof 18