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Magnetic Resonance in Medicine|April 5, 2012
Dynamic monitoring of carnitine and acetylcarnitine in the trimethylamine signal after exercise in human skeletal muscle by 7T 1H-MRSJimin Ren, Susan Lakoski, Ronald G Haller, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|August 5, 2011
Exertional dyspnea in mitochondrial myopathy: clinical features and physiological mechanismsKatja Heinicke, Tanja Taivassalo, Phil Wyrick, et al.
American Journal of Human Genetics|August 12, 2009
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletionsHenna Tyynismaa, Emil Ylikallio, Mehul Patel, et al.
American Journal of Physiology. Endocrinology and Metabolism|June 7, 2007
The effect of training on the expression of mitochondrial biogenesis- and apoptosis-related proteins in skeletal muscle of patients with mtDNA defectsPeter J Adhihetty, Tanja Taivassalo, Ronald G Haller, et al.
Brain : a Journal of Neurology|January 23, 2003
The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patientsTanja Taivassalo, Tina Dysgaard Jensen, Nancy Kennaway, et al.
Archives of Neurology|March 11, 2009
Fat metabolism during exercise in patients with mitochondrial diseaseTina Dysgaard Jeppesen, Mette Cathrine Orngreen, Gerrit van Hall, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 19, 2017
Metabolic profiles of exercise in patients with McArdle disease or mitochondrial myopathyNigel F Delaney, Rohit Sharma, Laura Tadvalkar, et al.
American Journal of Physiology. Endocrinology and Metabolism|May 15, 2002
Decreased insulin action in skeletal muscle from patients with McArdle's diseaseJakob N Nielsen, John Vissing, Jørgen F P Wojtaszewski, et al.
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