Succinate dehydrogenase deficiency: A qualitative and quantitative assessment in muscle

Archives of Pathology and Laboratory Medicine

Volumn 124, Issue 12, 2000, Pages 1755-1758

  Vladutiu, G D ^a   Heffner, R R ^a  

^a UNIVERSITY AT BUFFALO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SUCCINATE DEHYDROGENASE;

ARTICLE; ENZYME ACTIVITY; ENZYME DEFICIENCY; GENE MUTATION; GENETIC DISORDER; HUMAN; HUMAN TISSUE; MITOCHONDRIAL MEMBRANE; MITOCHONDRIAL MYOPATHY; MUSCLE BIOPSY; QUALITATIVE DIAGNOSIS; QUANTITATIVE ASSAY; RESPIRATORY CHAIN; RISK ASSESSMENT; SOMATIC MUTATION;

ADOLESCENT; ADULT; AGED; BIOPSY; CHILD; CHILD, PRESCHOOL; FEMALE; HISTOCYTOCHEMISTRY; HUMANS; INFANT; MALE; MIDDLE AGED; MITOCHONDRIAL MYOPATHIES; MUSCLE, SKELETAL; SUCCINATE DEHYDROGENASE;

EID: 0033638951     PISSN: 00039985     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. Quantitative succinate dehydrogenase analysis in normal and ragged-red muscle fibers
2. Structure and function of succinate dehydrogenase and fumarate reductase
3. Deficiencies of NADH and succinate dehydrogenases in degenerative diseases and myopathies
4. Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency: Abnormalities of several iron-sulfur proteins
5. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
6. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
7. Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome
8. Deficiency of complex II of the mitochondrial respiratory chain in late onset optic atrophy and ataxia
9. Kearns-Sayre syndrome and complex II deficiency
10. Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria
11. Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory Chain
12. Hypertrophic cardiomyopathy with mitochondrial myopathy: A new phenotype of complex II defect
13. Preparation of succinate dehydrogenase and reconstitution of succinate oxidase
14. Citrate synthase activity in skeletal muscle
15. The expanding clinical spectrum of mitochondrial diseases