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R G Haller

Showing results (21-30 of 57) with videos related to

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Journal of Applied Physiology (Bethesda, Md. : 1985)|May 1, 1992
Effect of deficient muscular glycogenolysis on extramuscular fuel production in exerciseJ Vissing, S F Lewis, H Galbo, et al.
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.
Transactions of the American Neurological Association|January 1, 1979
A "lipid myopathy" associated with a hyperkinetic circulatory response to exerciseR G Haller, J D Cook, S Lewis, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|January 21, 2000
A modular NIRS system for clinical measurement of impaired skeletal muscle oxygenationR Wariar, J N Gaffke, R G Haller, et al.
Neurology|April 1, 1984
Serum and muscle potassium in experimental alcoholic myopathyR G Haller, N W Carter, E Ferguson, et al.
Transactions of the American Neurological Association|January 1, 1978
Mitochondrial myopathy presenting as exercise intoleranceR G Haller, A Mukherjee, F A Gaffney, et al.
Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology|December 1, 1984
Metabolic control of cardiac output response to exercise in McArdle's diseaseS F Lewis, R G Haller, J D Cook, et al.
Annals of Neurology|October 1, 1994
Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patientsS Tsujino, S Shanske, A K Brownell, et al.
Physiology & Behavior|January 1, 1977
Ileum motility of monkeys during chronic avoidance conditioning pre- and post-cingulumotomyJ S Lockard, E L Foltz, A L Ehle, 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.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Journal of Applied Physiology (Bethesda, Md. : 1985)|May 1, 1992
Effect of deficient muscular glycogenolysis on extramuscular fuel production in exerciseJ Vissing, S F Lewis, H Galbo, et al.
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.
Transactions of the American Neurological Association|January 1, 1979
A "lipid myopathy" associated with a hyperkinetic circulatory response to exerciseR G Haller, J D Cook, S Lewis, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|January 21, 2000
A modular NIRS system for clinical measurement of impaired skeletal muscle oxygenationR Wariar, J N Gaffke, R G Haller, et al.
Neurology|April 1, 1984
Serum and muscle potassium in experimental alcoholic myopathyR G Haller, N W Carter, E Ferguson, et al.
Transactions of the American Neurological Association|January 1, 1978
Mitochondrial myopathy presenting as exercise intoleranceR G Haller, A Mukherjee, F A Gaffney, et al.
Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology|December 1, 1984
Metabolic control of cardiac output response to exercise in McArdle's diseaseS F Lewis, R G Haller, J D Cook, et al.
Annals of Neurology|October 1, 1994
Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patientsS Tsujino, S Shanske, A K Brownell, et al.
Physiology & Behavior|January 1, 1977
Ileum motility of monkeys during chronic avoidance conditioning pre- and post-cingulumotomyJ S Lockard, E L Foltz, A L Ehle, 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.
Pageof 6