A patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiency-Reference-Cited by-同舟云学术

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A patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiency

Published:2000-05 Issue:3 Volume:22 Page:158-162
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Sugimoto Junko,Shimohira Masayuki,Osawa Yukiko,Matsubara Masaaki,Yamamoto Haruyasu,Goto Yu-ichi,Nonaka Ikuya

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain;Taylor;Biochim Biophys Acta,1993

2. Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase;Behbehani;Eur J Pediatr,1984

3. Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome;Bourgeois;Brain Dev,1992

4. Kearns-Sayre syndrome and complex II deficiency;Rivner;Neurology,1989

5. Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy and paroxysmal myoglobinuria;Linderholm;J Int Med,1990

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1. Connective tissue involvement in an m.10191 T > C carrier with Leigh-like syndrome;Bulletin of the National Research Centre;2023-12-15

2. Histochemical and immunohistochemical staining methods to visualize mitochondrial proteins and activity;Methods in Cell Biology;2020

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5. Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy;Brain and Development;2014-05

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