A riboflavin-responsive lipid storage myopathy due to multiple acyl-CoA dehydrogenase deficiency: An adult case-Reference-Cited by-同舟云学术

A riboflavin-responsive lipid storage myopathy due to multiple acyl-CoA dehydrogenase deficiency: An adult case

Published:1994-11 Issue:2 Volume:126 Page:202-205
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Araki Eiichi,Kobayashi Takuro,Kohtake Naoko,Goto Ikuo,Hashimoto Takashi

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference22 articles.

1. The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria;Amendt;J. Clin. Invest.,1986

2. Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of β-oxidation;Angelini;Crit. Rev. Clin. Lab. Sci.,1992

3. A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase;Aoyama;Biochem. Biophys. Res. Commun.,1993

4. Electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) deficiency in an adult;Bell;Neurology,1990

5. Riboflavin-responsive lipid myopathy and carnitine deficiency;Carroll;Neurology,1981

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