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R G Haller

Showing results (51-60 of 57) with videos related to

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Journal of Magnetic Resonance Imaging : JMRI|July 1, 1992
Effect of perfusion on exercised muscle: MR imaging evaluationB T Archer, J L Fleckenstein, L A Bertocci, et al.
Magnetic Resonance Quarterly|April 1, 1991
Locomotor system assessment by muscle magnetic resonance imagingJ L Fleckenstein, P T Weatherall, L A Bertocci, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|September 1, 1991
Absence of exercise-induced MRI enhancement of skeletal muscle in McArdle's diseaseJ L Fleckenstein, R G Haller, S F Lewis, 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.
The Journal of Clinical Investigation|October 1, 1991
Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defectR G Haller, K G Henriksson, L Jorfeldt, 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 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Journal of Magnetic Resonance Imaging : JMRI|July 1, 1992
Effect of perfusion on exercised muscle: MR imaging evaluationB T Archer, J L Fleckenstein, L A Bertocci, et al.
Magnetic Resonance Quarterly|April 1, 1991
Locomotor system assessment by muscle magnetic resonance imagingJ L Fleckenstein, P T Weatherall, L A Bertocci, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|September 1, 1991
Absence of exercise-induced MRI enhancement of skeletal muscle in McArdle's diseaseJ L Fleckenstein, R G Haller, S F Lewis, 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.
The Journal of Clinical Investigation|October 1, 1991
Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defectR G Haller, K G Henriksson, L Jorfeldt, 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 6