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Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.Annals of the New York Academy of Sciences|December 10, 1999
Peripheral neuropathy caused by proteolipid protein gene mutationsJ Y Garbern, F Cambi, R Lewis, et al.Annals of the New York Academy of Sciences|November 1, 2017
Peripheral Neuropathy Caused by Proteolipid Protein Gene MutationsJames Y Garbern, Franca Cambi, Richard Lewis, et al.Clinical and Experimental Immunology|January 29, 2021
IVIg increases interleukin-11 levels, which in turn contribute to increased platelets, VWF and FVIII in mice and humansA Nguyen, Y Repesse, M Ebbo, et al.Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.Neurology|August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutationsH Azzedine, N Ravisé, C Verny, et al.Revue Neurologique|December 21, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic strategy. Guidelines of the French CIDP study group]J C Antoine, J P Azulay, P Bouche, et al.Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.Brain : a Journal of Neurology|September 26, 2001
The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodiesH J Willison, C P O'Leary, J Veitch, et al.Neuron|July 1, 1997
Proteolipid protein is necessary in peripheral as well as central myelinJ Y Garbern, F Cambi, X M Tang, et al.Pageof 18