Showing results (21-30 of 871) with videos related to

Sort By:
Pageof 88
Neuromuscular Disorders : NMD|July 16, 2002
Congenital myasthenic syndrome associated with episodic apnea and sudden infant deathR F Byring, H Pihko, A Tsujino, et al.
Neurology|December 25, 2002
Congenital myasthenic syndrome caused by low-expressor fast-channel AChR delta subunit mutationX-M Shen, K Ohno, T Fukudome, et al.
The Journal of Clinical Investigation|November 24, 1999
Mutation causing congenital myasthenia reveals acetylcholine receptor beta/delta subunit interaction essential for assemblyP A Quiram, K Ohno, M Milone, et al.
Neurology|January 26, 2011
Myasthenic syndrome caused by plectinopathyD Selcen, V C Juel, L D Hobson-Webb, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2001
Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humansK Ohno, A Tsujino, J M Brengman, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Niemann-Pick disease types A and B]K Ohno
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Carbohydrate-deficient glycoprotein syndrome]K Ohno
Human Pathology|July 1, 1986
Mononuclear cells in myopathies: quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathiesA G Engel, K Arahata
Brain Research|November 18, 1996
Block of the endplate acetylcholine receptor channel by the sympathomimetic agents ephedrine, pseudoephedrine, and albuterolM Milone, A G Engel
European Journal of Biochemistry|May 15, 1985
Regulatory properties of a mutant carnitine palmitoyltransferase in human skeletal muscleS Zierz, A G Engel
Pageof 88