A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
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Mitochondrial myopathy: a genetic study of 71 casesMuscle coenzyme Q deficiency in familial mitochondrial encephalomyopathyEpilepsy in a mitochondrial disorder.Screening for mitochondrial cytopathies: the sub-anaerobic threshold exercise test (SATET).Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.Myopathy in vitamin E deficient rats: muscle fibre necrosis associated with disturbances of mitochondrial function.Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect.Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.Mutations in mitochondrial DNA as a cause of exercise intolerance.Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.Congenital deficiency of two polypeptide subunits of the iron-protein fragment of mitochondrial complex I.Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemiaMitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral diseaseDefective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia.Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.Mitochondrial functions in chronic spinal muscular atrophy.Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.Prevalence and progression of mitochondrial diseases: a study of 50 patients.Effect of Amytal on metabolism of perfused rat heart: relationship between glycolysis and oxidative phosphorylation.Intracellular pH governs the subcellular distribution of hexokinase in a glioma cell lineExperimentally induced defects of mitochondrial metabolism in rat skeletal muscle. Biological effects of the mitochondrial uncoupling agent 2,4-dinitrophenolExperimentally induced defects of mitochondrial metabolism in rat skeletal muscle. Biological effects of the NADH: coenzyme Q reductase inhibitor diphenyleneiodonium.[Myopathy due to succinate cytochrome C oxidoreductase deficiency: possible defect of complex II of the respiratory chain]Biochemical and genetic studies in a family with mitochondrial myopathy.An investigation of arterial insufficiency in rat hindlimb. An enzymic, mitochondrial and histological study.Biochemical adaptation in the skeletal muscle of rats depleted of creatine with the substrate analogue beta-guanidinopropionic acid.Tissue variation in the control of oxidative phosphorylation: implication for mitochondrial diseases.Mobilization of adenine nucleotide translocators as molecular bases of the biochemical threshold effect observed in mitochondrial diseases.Is bupivacaine a decoupler, a protonophore or a proton-leak-inducer?Abnormal mitochondria on a renal biopsy from a case of mitochondrial myopathy.Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene
P2860
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P2860
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年学术文章
@wuu
1977年学术文章
@zh
1977年学术文章
@zh-cn
1977年学术文章
@zh-hans
1977年学术文章
@zh-my
1977年学术文章
@zh-sg
1977年學術文章
@yue
1977年學術文章
@zh-hant
name
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
@en
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
@nl
type
label
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
@en
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
@nl
prefLabel
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
@en
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
@nl
P2093
P356
P1433
P1476
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
@en
P2093
Darveniza P
Morgan-Hughes JA
Sherratt RM
P304
P356
10.1093/BRAIN/100.4.617
P407
P577
1977-12-01T00:00:00Z