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European Journal of Neurology|February 18, 2017
Phenotypic spectrum of Charcot-Marie-Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patientsR Guimarães-Costa, R Iancu Ferfoglia, S Leonard-Louis, et al.
Neurology|August 13, 2008
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and SwedenP N Valdmanis, E Kabashi, A Dyck, et al.
Neurology|April 28, 2012
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutationsP Corcia, P Valdmanis, S Millecamps, et al.
Neurology|September 11, 2009
Mutations in FUS cause FALS and SALS in French and French Canadian populationsV V Belzil, P N Valdmanis, P A Dion, et al.
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