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Neurology
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October 1, 1983
Hyperkinetic circulation during exercise in neuromuscular disease
R G Haller, S F Lewis, J D Cook, et al.
Muscle & Nerve
|
October 1, 1989
Magnetic resonance imaging of muscle injury and atrophy in glycolytic myopathies
J L Fleckenstein, R M Peshock, S F Lewis, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
December 1, 1985
Muscle fatigue in McArdle's disease studied by 31P-NMR: effect of glucose infusion
S F Lewis, R G Haller, J D Cook, et al.
Annals of Neurology
|
February 1, 1985
Myophosphorylase deficiency impairs muscle oxidative metabolism
R G Haller, S F Lewis, J D Cook, et al.
Clinical Science (London, England : 1979)
|
June 1, 1995
Tricarboxylic acid cycle intermediates during incremental exercise in healthy subjects and in patients with McArdle's disease
K Sahlin, L Jorfeldt, K G Henriksson, et al.
The American Journal of Medicine
|
February 1, 1983
Low muscle levels of pyridoxine in McArdle's syndrome
R G Haller, W B Dempsey, H Feit, et al.
The Journal of Physiology
|
December 4, 2001
The exercise metaboreflex is maintained in the absence of muscle acidosis: insights from muscle microdialysis in humans with McArdle's disease
J Vissing, D A MacLean, S F Vissing, et al.
Radiology
|
April 1, 1992
Glycogenolysis, not perfusion, is the critical mediator of exercise-induced muscle modifications on MR images
J L Fleckenstein, R G Haller, L A Bertocci, et al.
The Journal of Clinical Investigation
|
December 1, 1993
Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins
R E Hall, K G Henriksson, S F Lewis, et al.
The Journal of Clinical Investigation
|
May 1, 1990
Impairment of sympathetic activation during static exercise in patients with muscle phosphorylase deficiency (McArdle's disease)
S L Pryor, S F Lewis, R G Haller, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 57) with videos related to
Sort By:
Page
of 6
Neurology
|
October 1, 1983
Hyperkinetic circulation during exercise in neuromuscular disease
R G Haller, S F Lewis, J D Cook, et al.
Muscle & Nerve
|
October 1, 1989
Magnetic resonance imaging of muscle injury and atrophy in glycolytic myopathies
J L Fleckenstein, R M Peshock, S F Lewis, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
December 1, 1985
Muscle fatigue in McArdle's disease studied by 31P-NMR: effect of glucose infusion
S F Lewis, R G Haller, J D Cook, et al.
Annals of Neurology
|
February 1, 1985
Myophosphorylase deficiency impairs muscle oxidative metabolism
R G Haller, S F Lewis, J D Cook, et al.
Clinical Science (London, England : 1979)
|
June 1, 1995
Tricarboxylic acid cycle intermediates during incremental exercise in healthy subjects and in patients with McArdle's disease
K Sahlin, L Jorfeldt, K G Henriksson, et al.
The American Journal of Medicine
|
February 1, 1983
Low muscle levels of pyridoxine in McArdle's syndrome
R G Haller, W B Dempsey, H Feit, et al.
The Journal of Physiology
|
December 4, 2001
The exercise metaboreflex is maintained in the absence of muscle acidosis: insights from muscle microdialysis in humans with McArdle's disease
J Vissing, D A MacLean, S F Vissing, et al.
Radiology
|
April 1, 1992
Glycogenolysis, not perfusion, is the critical mediator of exercise-induced muscle modifications on MR images
J L Fleckenstein, R G Haller, L A Bertocci, et al.
The Journal of Clinical Investigation
|
December 1, 1993
Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins
R E Hall, K G Henriksson, S F Lewis, et al.
The Journal of Clinical Investigation
|
May 1, 1990
Impairment of sympathetic activation during static exercise in patients with muscle phosphorylase deficiency (McArdle's disease)
S L Pryor, S F Lewis, R G Haller, et al.
Page
of 6