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Mitochondrial encephalomyopathies
scientific article published on 01 August 1988
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scholarly article
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 October 2019
review article
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Europe PubMed Central
title
Mitochondrial encephalomyopathies
(English)
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 October 2019
author name string
Peterson PL
series ordinal
1
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
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9 October 2019
Martens ME
series ordinal
2
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
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9 October 2019
Lee CP
series ordinal
3
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
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9 October 2019
publication date
1 August 1988
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
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9 October 2019
published in
Neurologic Clinics
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stated in
Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 October 2019
volume
6
1 reference
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
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9 October 2019
page(s)
529-544
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Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
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9 October 2019
cites work
Kearns-Sayre syndrome with reduced plasma and cerebrospinal fluid folate
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Kearns syndrome: a heterogeneous group of disorders with CPEO, or a nosological entity?
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7 January 2021
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Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Mitochondrial myoneuropathy with respiratory failure and myoclonic epilepsy. A case report with biochemical studies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation product
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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The molecular aetiology of human mitochondrial myopathies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Spongiform encephalopathy with chronic progressive external ophthalmoplegia. Central ophthalmoplegia mimicking ocular myopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Muscle Carnitine Palmityltransferase Deficiency and Myoglobinuria
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Mitochondrial myopathies
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
retrieved
7 January 2021
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inferred from DOI database lookup
Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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The atypical pigmentary retinopathy of Kearns-Sayre syndrome. A light and electron microscopic study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Enzymic Activities of Human Skeletal Muscle Mitochondria: A Tool in Clinical Metabolic Research
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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DT diaphorase. I. Purification from the soluble fraction of rat-liver cytoplasm, and properties
1 reference
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Trichopoliodystrophy. I. Report of a case and biochemical studies
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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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
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Crossref
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7 January 2021
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Strokelike episodes in MERRF.
1 reference
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Familial spongy degeneration of the central nervous system (Van Bogaert-Bertrand disease). An ultrastructural study.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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The syndrome of myoclonic epilepsy with ragged-red fibers. Report of a case and review of the literature
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Clinical improvement after administration of coenzyme Q10 in a patient with mitochondrial encephalomyopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Kearns-Sayre syndrome with hypoparathyroidism
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Regulation of respiration and ATP synthesis in higher organisms: hypothesis
1 reference
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7 January 2021
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Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Biogenesis of mitochondria and genetics of mitochondrial defects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Subacute necrotizing encephalomyelopathy in an infant
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical studies of skeletal muscle mitochondria. I. Microanalysis of cytochrome content, oxidative and phosphorylative activities of mammalian skeletal muscle mitochondria
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Kearns-Sayre syndrome: biochemical studies of mitochondrial metabolism
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic disorders of mitochondrial function
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
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Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal mitochondrial cardiomyopathy in Kearns-Sayre syndrome with deficiency of cytochrome-c-oxidase in cardiac and skeletal muscle. An enzymehistochemical--ultra-immunocytochemical--fine structural study in longterm frozen autopsy tissue.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The retinal manifestations of mitochondrial myopathy. A study of 22 cases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial encephalomyopathy with cardiomyopathy. A case revealing a defect of complex I in the respiratory chain
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Improvement of abnormal pyruvate metabolism and cardiac conduction defect with coenzyme Q10 in Kearns-Sayre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
retrieved
7 January 2021
based on heuristic
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Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
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Therapy of mitochondrial disorders
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
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Maternally inherited mitochondrial myopathy and myoclonic epilepsy.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reversible alexia, mitochondrial myopathy, and lactic acidemia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Peripheral neuropathy associated with mitochondrial myopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930859-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0733-8619(18)30859-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 October 2019
PubMed publication ID
3065599
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3065599
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3065599%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 October 2019
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