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FEBS Letters|December 16, 1991
Two isoforms of the muscle acetylcholine receptor alpha-subunit are translated in the human cell line TE671A Morris, D Beeson, L Jacobson, et al.Journal of the Neurological Sciences|March 20, 1997
Incidence of serum anti-P/O-type and anti-N-type calcium channel autoantibodies in the Lambert-Eaton myasthenic syndromeM Motomura, B Lang, I Johnston, et al.Journal of Neuroimmunology|July 1, 1993
Presentation of endogenous acetylcholine receptor epitope by an MHC class II-transfected human muscle cell line to a specific CD4+ T cell clone from a myasthenia gravis patientF Baggi, M Nicolle, A Vincent, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1991
Immunological evidence for the co-existence of the Lambert-Eaton myasthenic syndrome and myasthenia gravis in two patientsJ Newsom-Davis, K Leys, A Vincent, et al.Neurology|April 14, 2004
Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndromeR Webster, M Brydson, R Croxen, et al.Immunology|May 1, 1986
Anti-acetylcholine receptor antibodies induced in mice by syngeneic receptor without adjuvantsG K Scadding, L Calder, A Vincent, et al.Muscle & Nerve|December 1, 1994
Passive transfer of seronegative myasthenia gravis to miceJ Burges, A Vincent, P C Molenaar, et al.Annals of Neurology|October 1, 1991
Seronegative myasthenia gravis: a plasma factor inhibiting agonist-induced acetylcholine receptor function copurifies with IgMT Yamamoto, A Vincent, T A Ciulla, et al.The Cochrane Database of Systematic Reviews|June 14, 2003
Treatment for Lambert-Eaton myasthenic syndromeP Maddison, J Newsom-DavisThe Cochrane Database of Systematic Reviews|April 23, 2005
Treatment for Lambert-Eaton myasthenic syndromeP Maddison, J Newsom-DavisPageof 132