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Neuromuscular Disorders : NMD
|
June 3, 1998
Congenital myasthenic syndromes: gene mutation
K Ohno, A G Engel
Annals of the New York Academy of Sciences
|
January 1, 1987
The membrane attack complex of complement at the endplate in myasthenia gravis
A G Engel, K Arahata
Annals of Neurology
|
February 1, 1988
Monoclonal antibody analysis of mononuclear cells in myopathies. IV: Cell-mediated cytotoxicity and muscle fiber necrosis
K Arahata, A G Engel
The Biochemical Journal
|
July 1, 1987
Different sites of inhibition of carnitine palmitoyltransferase by malonyl-CoA, and by acetyl-CoA and CoA, in human skeletal muscle
S Zierz, A G Engel
No to Shinkei = Brain and Nerve
|
February 7, 1998
[New insights into congenital myasthenic syndromes]
K Ohno, A G Engel
Annals of Neurology
|
December 1, 1992
Expression of 65-kd heat shock proteins in the inflammatory myopathies
R Hohlfeld, A G Engel
Journal of Medical Genetics
|
January 20, 2004
Lack of founder haplotype for the rapsyn N88K mutation: N88K is an ancient founder mutation or arises from multiple founders
K Ohno, A G Engel
Neurology
|
December 1, 1975
Duchenne dystrophy: electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber
B Mokri, A G Engel
Annals of Neurology
|
February 1, 1986
Monoclonal antibody analysis of mononuclear cells in myopathies. III: Immunoelectron microscopy aspects of cell-mediated muscle fiber injury
K Arahata, A G Engel
Annals of the New York Academy of Sciences
|
September 15, 1971
Histometric analysis of the ultrastructure of the neuromuscular junction in myasthenia gravis and in the myasthenic syndrome
A G Engel, T Santa
Page
of 25
Search research articles
Search
Showing results (31-40 of 242) with videos related to
Sort By:
Page
of 25
Neuromuscular Disorders : NMD
|
June 3, 1998
Congenital myasthenic syndromes: gene mutation
K Ohno, A G Engel
Annals of the New York Academy of Sciences
|
January 1, 1987
The membrane attack complex of complement at the endplate in myasthenia gravis
A G Engel, K Arahata
Annals of Neurology
|
February 1, 1988
Monoclonal antibody analysis of mononuclear cells in myopathies. IV: Cell-mediated cytotoxicity and muscle fiber necrosis
K Arahata, A G Engel
The Biochemical Journal
|
July 1, 1987
Different sites of inhibition of carnitine palmitoyltransferase by malonyl-CoA, and by acetyl-CoA and CoA, in human skeletal muscle
S Zierz, A G Engel
No to Shinkei = Brain and Nerve
|
February 7, 1998
[New insights into congenital myasthenic syndromes]
K Ohno, A G Engel
Annals of Neurology
|
December 1, 1992
Expression of 65-kd heat shock proteins in the inflammatory myopathies
R Hohlfeld, A G Engel
Journal of Medical Genetics
|
January 20, 2004
Lack of founder haplotype for the rapsyn N88K mutation: N88K is an ancient founder mutation or arises from multiple founders
K Ohno, A G Engel
Neurology
|
December 1, 1975
Duchenne dystrophy: electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber
B Mokri, A G Engel
Annals of Neurology
|
February 1, 1986
Monoclonal antibody analysis of mononuclear cells in myopathies. III: Immunoelectron microscopy aspects of cell-mediated muscle fiber injury
K Arahata, A G Engel
Annals of the New York Academy of Sciences
|
September 15, 1971
Histometric analysis of the ultrastructure of the neuromuscular junction in myasthenia gravis and in the myasthenic syndrome
A G Engel, T Santa
Page
of 25