Exercise Testing in Metabolic Myopathies Journal Articles

abstract

• Metabolic myopathies are a group of genetic disorders specifically affecting glucose/glycogen, lipid, and mitochondrial metabolism. The main metabolic myopathies that are evaluated in this article are the mitochondrial myopathies, fatty acid oxidation defects, and glycogen storage disease. This article focuses on the usefulness of exercise in the evaluation of genetic metabolic myopathies.

authors

• Tarnopolsky, Mark

status

• published 

publication date

• February 2012

has subject area

• 3-Hydroxyacyl CoA Dehydrogenases (MeSH)
• Acetyl-CoA C-Acyltransferase (MeSH)
• Carbon-Carbon Double Bond Isomerases (MeSH)
• Enoyl-CoA Hydratase (MeSH)
• Exercise Test (MeSH)
• Exercise Tolerance (MeSH)
• Glycogen Storage Disease (MeSH)
• Humans (MeSH)
• Mitochondrial Myopathies (MeSH)
• Muscle Contraction (MeSH)
• Muscle, Skeletal (MeSH)
• Racemases and Epimerases (MeSH)
• Rehabilitation (Science Metrix)

published in

• Physical Medicine and Rehabilitation Clinics of North America  Journal

keywords

• 3-Hydroxyacyl CoA Dehydrogenases
• Acetyl-CoA C-Acyltransferase
• Carbon-Carbon Double Bond Isomerases
• Enoyl-CoA Hydratase
• Exercise Test
• Exercise Tolerance
• Glycogen Storage Disease
• Humans
• Mitochondrial Myopathies
• Muscle Contraction
• Muscle, Skeletal
• Racemases and Epimerases

Digital Object Identifier (DOI)

• 10.1016/j.pmr.2011.11.011

PubMed ID

• 22239882

start page

• 173

end page

• 186

volume

• 23

issue

• 1