Systemic triglyceride storage disease with normal carnitine: a putative defect in long-chain fatty acid metabolism
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference23 articles.
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2. Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free diet;Askanas;Neurology,1985
3. Secondary carnitine insufficiency disorders of organic acid metabolism: modulation of acyl-CoACoA ratios by l-carnitine in vivo;Chalmers;Biochem. Soc. Trans.,1983
4. Neutral-lipid storage disease: a new disorder of lipid metabolism;Chanarin;Brit. Med. J.,1975
5. Mitochondrial myopathies: disorders of the respiratory chain and oxidative phosphorylation;Clark;J. Inher. Metab. Dis.,1984
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