Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: Clues to pathogenesis of Leigh disease-Reference-Cited by-同舟云学术

Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: Clues to pathogenesis of Leigh disease

Published:1987-02 Issue:2 Volume:110 Page:216-222
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Robinson Brian H.,De Meirieir Linda,Glerum Moira,Sherwood Geoffrey,Becker Larry

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference34 articles.

1. A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity;Morgan-Hughes;J Neurol Sci,1979

2. A mitochondrial myopathy with a respiratory chain defect and carnitine deficiency;Busch,1981

3. Progressive infantile poliodystrophy: association with disturbed pyruvate oxidation in muscle and liver;Prick;Arch Neurol,1981

4. Childhood mitochondrial myopathy with oppthalmoplegia;Land;J Neurol Sci,1981

5. Mitochondrial myopathy: biochemical studies revealing a deficiency of NADH-cytochrome b reductase activity;Land;J Neurol Sci,1981

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