Author:
Korenke G. -C.,Bentlage H. A. C. M.,Ruitenbeek W.,Sengers R. C. A.,Sperl W.,Trijbels J. M. F.,Gabreels F. J. M.,Wijburg F. A.,Wiedermann V.,Hanefeld F.,Wendel U.,Reckmann M.,Griebel V.,Wölk H.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference35 articles.
1. Arts WFM, Scholte HR, Bogaard JM, Kerrebijn KF, Luyt-Houwen JEM (1983) NADH-CoQ reductase deficient myopathy: successful treatment with riboflavine. Lancet II:581–582
2. Brown GK, Haan EA, Kirby DM, Scholem RD, Wraith JE, Rogers JG, Danks DM (1988) “Cerebral” lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis. Eur J Pediatr 147:10–14
3. Cooperstein SJ, Lazarow A (1951) A microspectrophotometric method for the determination of cytochrome oxidase. J Biol Chem 189:665–670
4. DiMauro S, Zeviani M, Servidei S, Prelle A, Miranda AF, Bonilla E, Schon E (1988) Biochemical and molecular aspects of cytochrome c oxidase deficiency. Adv Neurol 48:93–105
5. Fischer JC, Ruitenbeek W, Gabreels FJM, Janssen AJM, Renier WO, Sengers RCA, Stadhouders AM, Ter Laak HJ, Trijbels JMF, Veerkamp JHA (1986) A mitochondrial myopathy: the first case with an established defect at the level of coenzyme Q. Eur J Pediatr 144:441–444
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