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R G Haller
S F Lewis

Neurology

Showing results (1-10 of 10) with videos related to

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Neurology|May 1, 1986
Abnormal ventilation during exercise in McArdle's syndrome: modulation by substrate availabilityR G Haller, S F Lewis
Neurology|October 1, 1983
Hyperkinetic circulation during exercise in neuromuscular diseaseR G Haller, S F Lewis, J D Cook, et al.
Neurology|September 1, 1996
Paradoxically enhanced glucose production during exercise in humans with blocked glycolysis caused by muscle phosphofructokinase deficiencyJ Vissing, H Galbo, R G Haller
Neurology|January 27, 1998
Reduced levels of skeletal muscle Na+K+ -ATPase in McArdle diseaseR G Haller, T Clausen, J Vissing
Neurology|November 18, 1998
Oral branched-chain amino acids do not improve exercise capacity in McArdle diseaseD MacLean, J Vissing, S F Vissing, et al.
Neurology|April 1, 1984
Serum and muscle potassium in experimental alcoholic myopathyR G Haller, N W Carter, E Ferguson, et al.
Neurology|June 1, 1982
Kinetics of carnitine-dependent fatty acid oxidation: implications for human carnitine deficiencyC S Long, R G Haller, D W Foster, et al.
Neurology|February 25, 2009
Fat metabolism during exercise in patients with McArdle diseaseM C Ørngreen, T D Jeppesen, S Tvede Andersen, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
Neurology|May 1, 1997
Mitochondrial encephalomyopathy with coenzyme Q10 deficiencyC Sobreira, M Hirano, S Shanske, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Neurology|May 1, 1986
Abnormal ventilation during exercise in McArdle's syndrome: modulation by substrate availabilityR G Haller, S F Lewis
Neurology|October 1, 1983
Hyperkinetic circulation during exercise in neuromuscular diseaseR G Haller, S F Lewis, J D Cook, et al.
Neurology|September 1, 1996
Paradoxically enhanced glucose production during exercise in humans with blocked glycolysis caused by muscle phosphofructokinase deficiencyJ Vissing, H Galbo, R G Haller
Neurology|January 27, 1998
Reduced levels of skeletal muscle Na+K+ -ATPase in McArdle diseaseR G Haller, T Clausen, J Vissing
Neurology|November 18, 1998
Oral branched-chain amino acids do not improve exercise capacity in McArdle diseaseD MacLean, J Vissing, S F Vissing, et al.
Neurology|April 1, 1984
Serum and muscle potassium in experimental alcoholic myopathyR G Haller, N W Carter, E Ferguson, et al.
Neurology|June 1, 1982
Kinetics of carnitine-dependent fatty acid oxidation: implications for human carnitine deficiencyC S Long, R G Haller, D W Foster, et al.
Neurology|February 25, 2009
Fat metabolism during exercise in patients with McArdle diseaseM C Ørngreen, T D Jeppesen, S Tvede Andersen, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
Neurology|May 1, 1997
Mitochondrial encephalomyopathy with coenzyme Q10 deficiencyC Sobreira, M Hirano, S Shanske, et al.
Pageof 1