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A G Engel

Showing results (81-90 of 242) with videos related to

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The American Journal of Medicine|March 1, 1978
Acid maltase deficiency in adults presenting as respiratory failureE C Rosenow, A G Engel
Journal of Neuropathology and Experimental Neurology|November 1, 1982
Ultrastructural aspects of acetylcholine receptor turnover at the normal end-plate and in autoimmune myasthenia gravisG Fumagalli, A G Engel, J Lindstrom
Neurology|June 1, 1991
Necrotizing myopathy with pipestem capillaries, microvascular deposition of the complement membrane attack complex (MAC), and minimal cellular infiltrationA M Emslie-Smith, A G Engel
The American Journal of Pathology|May 1, 1995
Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathiesJ L De Bleecker, A G Engel
Mayo Clinic Proceedings|December 1, 1982
Estimation of degradation rate of acetylcholine receptor by external gamma counting in vivoG Fumagalli, A G Engel, J Lindstrom
Neurology|June 13, 2001
The earliest pathologic alterations in dysferlinopathyD Selcen, G Stilling, A G Engel
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1999
Serum choline activates mutant acetylcholine receptors that cause slow channel congenital myasthenic syndromesM Zhou, A G Engel, A Auerbach
Annals of the New York Academy of Sciences|January 1, 1981
The immunopathology of acquired myasthenia gravisA G Engel, K Sahashi, G Fumagalli
Annals of Neurology|April 1, 1990
Microvascular changes in early and advanced dermatomyositis: a quantitative studyA M Emslie-Smith, A G Engel
Bailliere'S Clinical Neurology|November 1, 1993
Cellular mechanisms in inflammatory myopathiesR Hohlfeld, N Goebels, A G Engel
Pageof 25

Showing results (81-90 of 242) with videos related to

Sort By:
Pageof 25
The American Journal of Medicine|March 1, 1978
Acid maltase deficiency in adults presenting as respiratory failureE C Rosenow, A G Engel
Journal of Neuropathology and Experimental Neurology|November 1, 1982
Ultrastructural aspects of acetylcholine receptor turnover at the normal end-plate and in autoimmune myasthenia gravisG Fumagalli, A G Engel, J Lindstrom
Neurology|June 1, 1991
Necrotizing myopathy with pipestem capillaries, microvascular deposition of the complement membrane attack complex (MAC), and minimal cellular infiltrationA M Emslie-Smith, A G Engel
The American Journal of Pathology|May 1, 1995
Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathiesJ L De Bleecker, A G Engel
Mayo Clinic Proceedings|December 1, 1982
Estimation of degradation rate of acetylcholine receptor by external gamma counting in vivoG Fumagalli, A G Engel, J Lindstrom
Neurology|June 13, 2001
The earliest pathologic alterations in dysferlinopathyD Selcen, G Stilling, A G Engel
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1999
Serum choline activates mutant acetylcholine receptors that cause slow channel congenital myasthenic syndromesM Zhou, A G Engel, A Auerbach
Annals of the New York Academy of Sciences|January 1, 1981
The immunopathology of acquired myasthenia gravisA G Engel, K Sahashi, G Fumagalli
Annals of Neurology|April 1, 1990
Microvascular changes in early and advanced dermatomyositis: a quantitative studyA M Emslie-Smith, A G Engel
Bailliere'S Clinical Neurology|November 1, 1993
Cellular mechanisms in inflammatory myopathiesR Hohlfeld, N Goebels, A G Engel
Pageof 25