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Neurology
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April 1, 1972
Histometric study of neuromuscular junction ultrastructure. II. Myasthenic syndrome
T Santa, A G Engel, E G Lambert
Journal of Neuropathology and Experimental Neurology
|
August 1, 1997
Myofibrillar myopathy. III. Abnormal expression of cyclin-dependent kinases and nuclear proteins
S Nakano, A G Engel, I Akiguchi, et al.
Annals of Neurology
|
January 1, 1996
Sporadic inclusion body myositis: counts of different types of abnormal fibers
J N Pruitt, C J Showalter, A G Engel
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1982
Acetylcholinesterase of human erythrocytes and neuromuscular junctions: homologies revealed by monoclonal antibodies
D M Fambrough, A G Engel, T L Rosenberry
Neurology
|
August 1, 1972
Progressive ataxia, retinal degeneration, neuromyopathy, and mental subnormality in a patient with true hypoparathyroidism, dwarfism, malabsorption, and cholelithiasis
M R Gomez, A G Engel, P J Dyck
Annals of Neurology
|
April 1, 1977
A new myasthenic syndrome with end-plate acetylcholinesterase deficiency, small nerve terminals, and reduced acetylcholine release
A G Engel, E H Lambert, M R Gomez
Annals of the New York Academy of Sciences
|
January 1, 1976
Experimental acetylcholine blockade of the neuromuscular junction. Effects on end plate and muscle fiber ultrastructure
S S Freeman, A G Engel, D B Drachman
The Journal of Experimental Medicine
|
December 1, 1992
Autoaggressive myocytotoxic T lymphocytes expressing an unusual gamma/delta T cell receptor
G Pluschke, D Rüegg, R Hohlfeld, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 5, 1998
Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme
K Ohno, J Brengman, A Tsujino, et al.
Mayo Clinic Proceedings
|
October 1, 1971
Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers
A G Engel, M R Gomez, R V Groover
Page
of 25
Search research articles
Search
Showing results (121-130 of 242) with videos related to
Sort By:
Page
of 25
Neurology
|
April 1, 1972
Histometric study of neuromuscular junction ultrastructure. II. Myasthenic syndrome
T Santa, A G Engel, E G Lambert
Journal of Neuropathology and Experimental Neurology
|
August 1, 1997
Myofibrillar myopathy. III. Abnormal expression of cyclin-dependent kinases and nuclear proteins
S Nakano, A G Engel, I Akiguchi, et al.
Annals of Neurology
|
January 1, 1996
Sporadic inclusion body myositis: counts of different types of abnormal fibers
J N Pruitt, C J Showalter, A G Engel
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1982
Acetylcholinesterase of human erythrocytes and neuromuscular junctions: homologies revealed by monoclonal antibodies
D M Fambrough, A G Engel, T L Rosenberry
Neurology
|
August 1, 1972
Progressive ataxia, retinal degeneration, neuromyopathy, and mental subnormality in a patient with true hypoparathyroidism, dwarfism, malabsorption, and cholelithiasis
M R Gomez, A G Engel, P J Dyck
Annals of Neurology
|
April 1, 1977
A new myasthenic syndrome with end-plate acetylcholinesterase deficiency, small nerve terminals, and reduced acetylcholine release
A G Engel, E H Lambert, M R Gomez
Annals of the New York Academy of Sciences
|
January 1, 1976
Experimental acetylcholine blockade of the neuromuscular junction. Effects on end plate and muscle fiber ultrastructure
S S Freeman, A G Engel, D B Drachman
The Journal of Experimental Medicine
|
December 1, 1992
Autoaggressive myocytotoxic T lymphocytes expressing an unusual gamma/delta T cell receptor
G Pluschke, D Rüegg, R Hohlfeld, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 5, 1998
Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme
K Ohno, J Brengman, A Tsujino, et al.
Mayo Clinic Proceedings
|
October 1, 1971
Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers
A G Engel, M R Gomez, R V Groover
Page
of 25