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English
Defects of the respiratory chain.
scientific article published on September 1990
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Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
review article
1 reference
stated in
Europe PubMed Central
title
Defects of the respiratory chain
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
author
Laurence Bindoff
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
author name string
Turnbull DM
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
publication date
1 September 1990
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
published in
Bailliere's clinical endocrinology and metabolism
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
volume
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
page(s)
583-619
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
cites work
Sequence and organization of the human mitochondrial genome
1 reference
stated in
Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Treatment of mitochondrial myopathy due to complex III deficiency with vitamins K3 and C: A 31P-NMR follow-up study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MITOCHONDRIAL FUNCTION IN PARKINSON'S DISEASE
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal lactic acidosis in infancy with a defect of complex III of the respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-chromosome localization of the functional gene for the E1 alpha subunit of the human pyruvate dehydrogenase complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficiencies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies: disorders of the respiratory chain and oxidative phosphorylation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for the existence of tissue specific isoenzymes of mitochondrial NADH dehydrogenase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA sequences homologous to mitochondrial genes in nuclei from normal rat tissues and from rat hepatoma cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy: tissue-specific expression of a defect in ubiquinol-cytochrome c reductase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spongiform encephalopathy with chronic progressive external ophthalmoplegia. Central ophthalmoplegia mimicking ocular myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second case
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in Leigh syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in three patients with Leigh's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cerebral metabolism of glucose and oxygen measured with positron tomography in patients with mitochondrial diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
The syndrome of myoclonic epilepsy with ragged-red fibers. Report of a case and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Magnetic resonance spectroscopy in the recognition of metabolic disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial protein import
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new mitochondrial myopathy. Biochemical studies revealing a deficiency in the cytochrome b-c1 complex (complex III) of the respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome-c-oxidase deficiency in a floppy infant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and molecular heterogeneity in patients with mitochondrial encephalomyopathies due to complex I deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of subunits of Complex I and mitochondrial encephalomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunocytochemical studies of cytochrome oxidase subunits in skeletal muscle of patients with partial cytochrome oxidase deficiencies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue-specific genes code for polypeptide VIa of bovine liver and heart cytochrome c oxidase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue- and species-specific expression of cytochrome c oxidase isozymes in vertebrates
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Systemic deficiency of the first component of the pyruvate dehydrogenase complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variability in the activity of respiratory chain enzymes in mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for Molecular Identity of Microsomal and Mitochondrial NADH-Cytochrome b5 Reductases of Rat Liver
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Childhood mitochondrial myopathy with ophthalmoplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regulation of palmitoylcarnitine oxidation in isolated rat liver mitochondria. Role of the redox state of NAD(H).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Subacute necrotizing encephalomyelopathy in an infant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue-specific genes for respiratory proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new type of mitochondrial encephalomyopathy with stroke-like episodes due to cytochrome oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two siblings with cytochromec oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine as a defect of brain oxidative metabolism: a hypothesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial function and superoxide generation from submitochondrial particles of aged rat hearts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Do Mitochondria Produce Oxygen Radicals in vivo?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome c oxidase deficiency in infancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Histiocytoid Cardiomyopathy of Infancy: Deficiency of Reducible Cytochrome b in Heart Mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormalities of the electron transport chain in idiopathic Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical features of mitochondrial myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Therapy of mitochondrial disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondria1 encephalomyopathy with decreased succinate-cytochrome c reductase activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Kearns-Sayre syndrome and complex II deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variable clinical presentation in patients with defective E1 component of pyruvate dehydrogenase complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive ophthalmoplegia. Report of cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of blood mitochondrial DNA in pancytopenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial complex I deficiency in Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DEOXYRIBONUCLEIC ACID ASSOCIATED WITH YEAST MITOCHONDRIA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inactivation of the gene encoding the 14-kDa subunit VII of yeast ubiquinol. Cytochrome c oxidoreductase and analysis of the resulting mutant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with special reference to the mechanism of cerebral manifestations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytochrome oxidase deficiency: immunological studies of skeletal muscle mitochondrial fractions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A cytochrome-related inherited disorder of the nervous system and muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The absorbance coefficient of beef heart cytochrome c1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A fourth case of fumarase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue specific defect of complex I of the mitochondrial respiratory chain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign reversible muscle cytochrome c oxidase deficiency: a second case
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fumarase deficiency: a new cause of mitochondrial encephalomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0950-351X%2805%2980069-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0950-351X(05)80069-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
PubMed publication ID
2176453
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2176453
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2176453%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
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