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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.
Neurologic Clinics|May 1, 1994
Congenital myasthenic syndromesA G Engel
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1980
Morphologic and immunopathologic findings in myasthenia gravis and in congenital myasthenic syndromesA G Engel
Annals of Neurology|November 1, 1984
Myasthenia gravis and myasthenic syndromesA G Engel
Journal of Child Neurology|October 1, 1988
Congenital myasthenic syndromesA G Engel
Neurology|October 21, 2011
Anti-MuSK autoantibodies block binding of collagen Q to MuSKY Kawakami, M Ito, M Hirayama, et al.
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