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A G Engel

Showing results (221-230 of 242) with videos related to

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Neurology|October 21, 2011
Anti-MuSK autoantibodies block binding of collagen Q to MuSKY Kawakami, M Ito, M Hirayama, et al.
Annals of the New York Academy of Sciences|June 21, 1993
The spectrum of congenital end-plate acetylcholinesterase deficiencyD O Hutchinson, A G Engel, T J Walls, et al.
Pediatric Research|May 1, 1983
Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride dietA M Glasgow, A G Engel, D M Bier, 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.
Annals of the New York Academy of Sciences|January 1, 1989
Motor nerve terminal calcium channels in Lambert-Eaton myasthenic syndrome. Morphologic evidence for depletion and that the depletion is mediated by autoantibodiesA G Engel, A Nagel, T Fukuoka, et al.
Neurology|January 26, 2011
Myasthenic syndrome caused by plectinopathyD Selcen, V C Juel, L D Hobson-Webb, et al.
Neurology|November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adultR B Bell, A K Brownell, C R Roe, 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.
Neuron|July 1, 1996
Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunitK Ohno, H L Wang, M Milone, et al.
Pageof 25

Showing results (221-230 of 242) with videos related to

Sort By:
Pageof 25
Neurology|October 21, 2011
Anti-MuSK autoantibodies block binding of collagen Q to MuSKY Kawakami, M Ito, M Hirayama, et al.
Annals of the New York Academy of Sciences|June 21, 1993
The spectrum of congenital end-plate acetylcholinesterase deficiencyD O Hutchinson, A G Engel, T J Walls, et al.
Pediatric Research|May 1, 1983
Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride dietA M Glasgow, A G Engel, D M Bier, 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.
Annals of the New York Academy of Sciences|January 1, 1989
Motor nerve terminal calcium channels in Lambert-Eaton myasthenic syndrome. Morphologic evidence for depletion and that the depletion is mediated by autoantibodiesA G Engel, A Nagel, T Fukuoka, et al.
Neurology|January 26, 2011
Myasthenic syndrome caused by plectinopathyD Selcen, V C Juel, L D Hobson-Webb, et al.
Neurology|November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adultR B Bell, A K Brownell, C R Roe, 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.
Neuron|July 1, 1996
Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunitK Ohno, H L Wang, M Milone, et al.
Pageof 25