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Circulation
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December 1, 1979
The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic studies
E N Prystowsky, E L Pritchett, A D Roses, et al.
Human Molecular Genetics
|
October 1, 1992
A chromosome 19 CA-dinucleotide repeat polymorphism
K L Phillips, J H Garbutt, A D Roses, et al.
Neurobiology of Disease
|
December 22, 1999
Apolipoprotein E expression by neurons surviving excitotoxic stress
U Boschert, E Merlo-Pich, G Higgins, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1974
Electron spin resonance studies of erythrocytes from patients with myotonic muscular dystrophy
D A Butterfield, D B Chesnut, A D Roses, et al.
Neurobiology of Disease
|
December 16, 1998
Uptake and internalization of exogenous apolipoprotein E3 by cultured human central nervous system neurons
K R Williams, A M Saunders, A D Roses, et al.
Muscle & Nerve
|
February 1, 1982
Myotonic muscular dystrophy: morphology, histochemistry, and growth characteristics of cultured skin fibroblasts
G B Hartwig, S E Miller, A P Frost, et al.
Neurology
|
August 1, 1981
Identification of abnormally [32P]-phosphorylated cyanogen bromide cleavage product of erythrocyte membrane spectrin in Duchenne muscular dystrophy
A D Roses, P E Shile, M H Herbstreith, et al.
Transactions of the American Neurological Association
|
January 1, 1979
The natural history of cardiac conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiology studies
E N Prystowsky, E L Pritchett, J J Gallagher, et al.
Electroencephalography and Clinical Neurophysiology. Supplement
|
January 1, 1978
Biochemical relationships between muscle and erythrocyte membrane. Interpretations with respect to Duchenne muscular dystrophy
A D Roses, M H Herbstreith, B S Metcalf, et al.
Neurology
|
October 1, 1979
LDH-5 levels and electrophoresis support media
A D Roses, M J Roses, G A Nicholson, et al.
Page
of 35
Search research articles
Search
Showing results (111-120 of 347) with videos related to
Sort By:
Page
of 35
Circulation
|
December 1, 1979
The natural history of conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiologic studies
E N Prystowsky, E L Pritchett, A D Roses, et al.
Human Molecular Genetics
|
October 1, 1992
A chromosome 19 CA-dinucleotide repeat polymorphism
K L Phillips, J H Garbutt, A D Roses, et al.
Neurobiology of Disease
|
December 22, 1999
Apolipoprotein E expression by neurons surviving excitotoxic stress
U Boschert, E Merlo-Pich, G Higgins, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1974
Electron spin resonance studies of erythrocytes from patients with myotonic muscular dystrophy
D A Butterfield, D B Chesnut, A D Roses, et al.
Neurobiology of Disease
|
December 16, 1998
Uptake and internalization of exogenous apolipoprotein E3 by cultured human central nervous system neurons
K R Williams, A M Saunders, A D Roses, et al.
Muscle & Nerve
|
February 1, 1982
Myotonic muscular dystrophy: morphology, histochemistry, and growth characteristics of cultured skin fibroblasts
G B Hartwig, S E Miller, A P Frost, et al.
Neurology
|
August 1, 1981
Identification of abnormally [32P]-phosphorylated cyanogen bromide cleavage product of erythrocyte membrane spectrin in Duchenne muscular dystrophy
A D Roses, P E Shile, M H Herbstreith, et al.
Transactions of the American Neurological Association
|
January 1, 1979
The natural history of cardiac conduction system disease in myotonic muscular dystrophy as determined by serial electrophysiology studies
E N Prystowsky, E L Pritchett, J J Gallagher, et al.
Electroencephalography and Clinical Neurophysiology. Supplement
|
January 1, 1978
Biochemical relationships between muscle and erythrocyte membrane. Interpretations with respect to Duchenne muscular dystrophy
A D Roses, M H Herbstreith, B S Metcalf, et al.
Neurology
|
October 1, 1979
LDH-5 levels and electrophoresis support media
A D Roses, M J Roses, G A Nicholson, et al.
Page
of 35