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A G Engel

Showing results (151-160 of 242) with videos related to

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Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndromes. New insights from molecular genetic and patch-clamp studiesA G Engel, K Ohno, M Milone, et al.
Annals of the New York Academy of Sciences|July 21, 1998
AChR channel blockade by quinidine sulfate reduces channel open duration in the slow-channel congenital myasthenic syndromeT Fukudome, K Ohno, J M Brengman, et al.
Progress in Brain Research|January 1, 1990
Newly recognized congenital myasthenic syndromes: I. Congenital paucity of synaptic vesicles and reduced quantal release. II. High-conductance fast-channel syndrome. III. Abnormal acetylcholine receptor (AChR) interaction with acetylcholine. IV. AChR deficiency and short channel-open timeA G Engel, T J Walls, A Nagel, et al.
Journal of the Neurological Sciences|December 1, 1989
Early ultrastructural alterations in adult dermatomyositis. Capillary abnormalities precede other structural changes in muscleM De Visser, A M Emslie-Smith, A G Engel
Acta Neurologica Scandinavica|July 1, 1975
Effects of microembolization on the skeletal muscle blood flow. A critique of the microvascular occlusion model of Duchenne dystrophyB Gudrun, G E Andrew, G Boysen, et al.
The New England Journal of Medicine|March 28, 1991
Polymyositis mediated by T lymphocytes that express the gamma/delta receptorR Hohlfeld, A G Engel, K Ii, et al.
Journal of the Neurological Sciences|November 1, 1974
Morphometric analysis of skeletal muscle capillary ultrastructure in inflammatory myopathiesF Jerusalem, M Rakusa, A G Engel, et al.
Neuroreport|July 17, 1998
Quinidine normalizes the open duration of slow-channel mutants of the acetylcholine receptorT Fukudome, K Ohno, J M Brengman, et al.
Journal of Neuropathology and Experimental Neurology|March 1, 1980
Ultrastructural localization of the terminal and lytic ninth complement component (C9) at the motor end-plate in myasthenia gravisK Sahashi, A G Engel, E H Lambert, et al.
Annals of the New York Academy of Sciences|January 1, 1976
The motor end plate in myasthenia gravis and in experimental autoimmune myasthenia gravis. A quantitative ultrastructural studyA G Engel, M Tsujihata, J M Lindstrom, et al.
Pageof 25

Showing results (151-160 of 242) with videos related to

Sort By:
Pageof 25
Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndromes. New insights from molecular genetic and patch-clamp studiesA G Engel, K Ohno, M Milone, et al.
Annals of the New York Academy of Sciences|July 21, 1998
AChR channel blockade by quinidine sulfate reduces channel open duration in the slow-channel congenital myasthenic syndromeT Fukudome, K Ohno, J M Brengman, et al.
Progress in Brain Research|January 1, 1990
Newly recognized congenital myasthenic syndromes: I. Congenital paucity of synaptic vesicles and reduced quantal release. II. High-conductance fast-channel syndrome. III. Abnormal acetylcholine receptor (AChR) interaction with acetylcholine. IV. AChR deficiency and short channel-open timeA G Engel, T J Walls, A Nagel, et al.
Journal of the Neurological Sciences|December 1, 1989
Early ultrastructural alterations in adult dermatomyositis. Capillary abnormalities precede other structural changes in muscleM De Visser, A M Emslie-Smith, A G Engel
Acta Neurologica Scandinavica|July 1, 1975
Effects of microembolization on the skeletal muscle blood flow. A critique of the microvascular occlusion model of Duchenne dystrophyB Gudrun, G E Andrew, G Boysen, et al.
The New England Journal of Medicine|March 28, 1991
Polymyositis mediated by T lymphocytes that express the gamma/delta receptorR Hohlfeld, A G Engel, K Ii, et al.
Journal of the Neurological Sciences|November 1, 1974
Morphometric analysis of skeletal muscle capillary ultrastructure in inflammatory myopathiesF Jerusalem, M Rakusa, A G Engel, et al.
Neuroreport|July 17, 1998
Quinidine normalizes the open duration of slow-channel mutants of the acetylcholine receptorT Fukudome, K Ohno, J M Brengman, et al.
Journal of Neuropathology and Experimental Neurology|March 1, 1980
Ultrastructural localization of the terminal and lytic ninth complement component (C9) at the motor end-plate in myasthenia gravisK Sahashi, A G Engel, E H Lambert, et al.
Annals of the New York Academy of Sciences|January 1, 1976
The motor end plate in myasthenia gravis and in experimental autoimmune myasthenia gravis. A quantitative ultrastructural studyA G Engel, M Tsujihata, J M Lindstrom, et al.
Pageof 25