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Neuron|July 1, 1995
Mutation of the acetylcholine receptor alpha subunit causes a slow-channel myasthenic syndrome by enhancing agonist binding affinityS M Sine, K Ohno, C Bouzat, et al.Annals of Neurology|June 1, 1996
MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathyK Ohno, M Yamamoto, A G Engel, et al.Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
Congenital myasthenic syndrome caused by prolonged acetylcholine receptor channel openings due to a mutation in the M2 domain of the epsilon subunitK Ohno, D O Hutchinson, M Milone, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 1, 1997
Slow-channel myasthenic syndrome caused by enhanced activation, desensitization, and agonist binding affinity attributable to mutation in the M2 domain of the acetylcholine receptor alpha subunitM Milone, H L Wang, K Ohno, et al.Neurology|July 22, 2009
Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patientsM Milone, X M Shen, D Selcen, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1980
Morphologic and immunopathologic findings in myasthenia gravis and in congenital myasthenic syndromesA G EngelNeurology|October 21, 2011
Anti-MuSK autoantibodies block binding of collagen Q to MuSKY Kawakami, M Ito, M Hirayama, et al.Pageof 88