Treatment of complex I deficiency with riboflavin
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference19 articles.
1. Biogenesis of flavoprotein and cytochrome components in hepatic mitochondria from riboflavin-deficient rats;Addison;Biochem. Biophys. Res. Commun.,1978
2. NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin;Arts;Lancet,1983
3. Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitine;Bernsen;Arch. Neurol.,1991
4. Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological and biochemical studies in muscle biopsies and autopsy tissues;Bresolin;Ann. Neurol.,1987
5. A mitochondrial myopathy with a respiratory chain defect and carnitine deficiency;Busch,1981
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