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Neuromuscular Disorders : NMD
|
January 15, 2004
Congenital myasthenic syndromes:gene mutations
Kinji Ohno, Andrew G Engel
Human Pathology
|
July 1, 1986
Mononuclear cells in myopathies: quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathies
A G Engel, K Arahata
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
December 1, 1983
Evidence for mediation by 5-HT2 receptors of 5-hydroxytryptamine-induced contraction of canine basilar artery
E Müller-Schweinitzer, G Engel
Brain Research
|
November 18, 1996
Block of the endplate acetylcholine receptor channel by the sympathomimetic agents ephedrine, pseudoephedrine, and albuterol
M Milone, A G Engel
Neuromuscular Disorders : NMD
|
February 24, 2001
Congenital myasthenic syndromes: gene mutations
K Ohno, A G Engel
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
March 23, 2006
Splicing abnormalities in congenital myasthenic syndromes
Kinji Ohno, Andrew G Engel
Human Genetics
|
September 13, 2005
Gene symbol: CHRNE. Disease: Endplate acetylcholine receptor deficiency
K Ohno, Andrew G Engel
European Journal of Biochemistry
|
May 15, 1985
Regulatory properties of a mutant carnitine palmitoyltransferase in human skeletal muscle
S Zierz, A G Engel
The Journal of Clinical Investigation
|
July 1, 1990
Lysis of myotubes by alloreactive cytotoxic T cells and natural killer cells. Relevance to myoblast transplantation
R Hohlfeld, A G Engel
Science (New York, N.Y.)
|
March 2, 1973
Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome
A G Engel, C Angelini
Page
of 75
Search research articles
Search
Showing results (61-70 of 741) with videos related to
Sort By:
Page
of 75
Neuromuscular Disorders : NMD
|
January 15, 2004
Congenital myasthenic syndromes:gene mutations
Kinji Ohno, Andrew G Engel
Human Pathology
|
July 1, 1986
Mononuclear cells in myopathies: quantitation of functionally distinct subsets, recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and implications for the pathogenesis of the different inflammatory myopathies
A G Engel, K Arahata
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
December 1, 1983
Evidence for mediation by 5-HT2 receptors of 5-hydroxytryptamine-induced contraction of canine basilar artery
E Müller-Schweinitzer, G Engel
Brain Research
|
November 18, 1996
Block of the endplate acetylcholine receptor channel by the sympathomimetic agents ephedrine, pseudoephedrine, and albuterol
M Milone, A G Engel
Neuromuscular Disorders : NMD
|
February 24, 2001
Congenital myasthenic syndromes: gene mutations
K Ohno, A G Engel
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
March 23, 2006
Splicing abnormalities in congenital myasthenic syndromes
Kinji Ohno, Andrew G Engel
Human Genetics
|
September 13, 2005
Gene symbol: CHRNE. Disease: Endplate acetylcholine receptor deficiency
K Ohno, Andrew G Engel
European Journal of Biochemistry
|
May 15, 1985
Regulatory properties of a mutant carnitine palmitoyltransferase in human skeletal muscle
S Zierz, A G Engel
The Journal of Clinical Investigation
|
July 1, 1990
Lysis of myotubes by alloreactive cytotoxic T cells and natural killer cells. Relevance to myoblast transplantation
R Hohlfeld, A G Engel
Science (New York, N.Y.)
|
March 2, 1973
Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome
A G Engel, C Angelini
Page
of 75