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Journal of Neurochemistry|April 1, 1995
Antigens associated with N- and L-type calcium channels in Lambert-Eaton myasthenic syndromeO el Far, B Marquèze, C Leveque, et al.American Journal of Medical Genetics|May 8, 2000
Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotypeL A Brueton, S M Huson, P M Cox, et al.Neurology|September 25, 2003
Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypesG Burke, J Cossins, S Maxwell, et al.Journal of Physiology, Paris|January 1, 1993
Synaptotagmin: a Lambert-Eaton myasthenic syndrome antigen that associates with presynaptic calcium channelsN Martin-Moutot, O el Far, C Leveque, et al.Human Immunology|October 20, 1999
A susceptibility region for myasthenia gravis extending into the HLA-class I sector telomeric to HLA-CM Janer, A Cowland, J Picard, et al.Proceedings of the National Academy of Sciences of the United States of America|August 15, 1991
Critical role for the Val/Gly86 HLA-DR beta dimorphism in autoantigen presentation to human T cellsB Ong, N Willcox, P Wordsworth, et al.Annals of the New York Academy of Sciences|July 21, 1998
Antibodies affecting ion channel function in acquired neuromyotonia, in seropositive and seronegative myasthenia gravis, and in antibody-mediated arthrogryposis multiplex congenitaA Vincent, L Jacobson, P Plested, et al.Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Human autoantibodies specific for the alpha1A calcium channel subunit reduce both P-type and Q-type calcium currents in cerebellar neuronsA Pinto, S Gillard, F Moss, et al.Lancet (London, England)|April 21, 1984
Controlled trial of plasma exchange in acute inflammatory polyradiculoneuropathyR J Greenwood, J Newsom-Davis, R A Hughes, et al.Brain : a Journal of Neurology|August 1, 1987
The slow channel syndrome. Two new casesH J Oosterhuis, J Newsom-Davis, J H Wokke, et al.Pageof 20