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Muscle & Nerve|January 12, 1999
Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B diseaseP Sindou, J M Vallat, F Chapon, et al.Brain : a Journal of Neurology|November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/CM Tazir, H Azzedine, S Assami, et al.Revue Neurologique|January 1, 1988
[Study of antiglycolipid antibodies in IgM monoclonal dysglobulinemias associated with peripheral neuropathy]M O Jauberteau, D Henin, P Bouche, et al.Human Mutation|January 1, 1997
Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 familiesH Rouger, E LeGuern, N Birouk, et al.Neuromuscular Disorders : NMD|October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathyR Zemmouri, H Azzedine, S Assami, et al.Neurology|February 24, 2010
Intramuscular interferon beta-1a in chronic inflammatory demyelinating polyradiculoneuropathyR A C Hughes, K C Gorson, D Cros, et al.Journal of the Neurological Sciences|January 15, 2009
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patientsM Tazir, L Ali-Pacha, A M'Zahem, et al.La Revue De Medecine Interne|October 15, 2010
[Small fibre neuropathy in primary Sjögren syndrome]A-L Fauchais, L Richard, G Gondran, et al.Molecular and Cellular Neurosciences|December 26, 2001
Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cellsD M Menichella, E J Arroyo, R Awatramani, et al.Neuromuscular Disorders : NMD|December 7, 2002
The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C geneM Chaouch, Y Allal, A De Sandre-Giovannoli, et al.Pageof 18