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Literature DB >> 3741216

Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration.

H Reichmann, R Rohkamm, M Zeviani, S Servidei, K Ricker, S DiMauro.

Abstract

Entities: Disease Gene

Mesh：

Substances：
Cytochrome b Group

Year: 1986 PMID： 3741216 DOI： 10.1001/archneur.1986.00520090081024

Source DB: PubMed Journal: Arch Neurol ISSN： 0003-9942

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11 in total

1. Emetine-induced myopathy and carnitine deficiency.

Authors: T Kuntzer; H Reichmann; J Bogousslavsky; F Regli
Journal: J Neurol Date: 1990-12 Impact factor: 4.849

Review 2. Mitochondrial myopathies.

Authors: S DiMauro; E Bonilla; M Zeviani; S Servidei; D C DeVivo; E A Schon
Journal: J Inherit Metab Dis Date: 1987 Impact factor: 4.982

3. Mitochondrial DNA mutations in multiple symmetric lipomatosis.

Authors: T Klopstock; M Naumann; P Seibel; B Shalke; K Reiners; H Reichmann
Journal: Mol Cell Biochem Date: 1997-09 Impact factor: 3.396

4. Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity.

Authors: W Sperl; W Ruitenbeek; J M Trijbels; R C Sengers; A M Stadhouders; J P Guggenbichler
Journal: Eur J Pediatr Date: 1988-05 Impact factor: 3.183

Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration.

1. Emetine-induced myopathy and carnitine deficiency.

Review 2. Mitochondrial myopathies.

3. Mitochondrial DNA mutations in multiple symmetric lipomatosis.

4. Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity.

5. Defects in the cytochrome bc1 complex in mitochondrial diseases.

6. Variability in the activity of respiratory chain enzymes in mitochondrial myopathies.

7. Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up study.

Review 8. The biochemical basis of mitochondrial diseases.

9. Myopathy in Williams-Beuren syndrome.

10. Stroke-like episodes in familial mitochondrial encephalomyopathy: clinical and biochemical aspects.