Publication year
2004Source
Annals of Neurology, 56, 2, (2004), pp. 279-83ISSN
Publication type
Article / Letter to editor
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Organization
Neurology
Journal title
Annals of Neurology
Volume
vol. 56
Issue
iss. 2
Page start
p. 279
Page end
p. 83
Subject
UMCN 3.1: Neuromuscular development and genetic disordersAbstract
Fuel utilization in two adult patients with the myopathic form of very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency and five healthy subjects was investigated with stable isotopes during exercise at 50% of VO2max. The findings indicate that residual VLCAD activity in the patients is sufficient to maintain normal oxidation of fat at rest, but that fat oxidation rate cannot increase above basal levels during exercise. This can cause an energy deficit and intramuscular accumulation of fat intermediates that may induce the exercise-induced symptoms.
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- Faculty of Medical Sciences [92292]
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