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Mitochondrial disorders in pediatrics. Clinical, biochemical, and genetic implications.
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scholarly article
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Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
review article
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Europe PubMed Central
title
Mitochondrial disorders in pediatrics. Clinical, biochemical, and genetic implications
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
author name string
L A Clarke
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
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English
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publication date
1 April 1992
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Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
published in
Pediatric Clinics of North America
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
volume
39
1 reference
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Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
page(s)
319-334
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
cites work
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%2FS0031-3955%2816%2938297-9
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%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isoforms of mammalian cytochrome c oxidase: correlation with human cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
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inferred from DOI database lookup
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of blood mitochondrial DNA in pancytopenia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies. Clinical, morphological and biochemical aspects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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%2FS0031-3955%2816%2938297-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
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%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2938297-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0031-3955(16)38297-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
PubMed publication ID
1553246
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1553246
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1553246%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
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