Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q68480752)
Watch
English
Mitochondrial encephalomyopathies
scientific article published on 01 August 1990
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
title
Mitochondrial encephalomyopathies
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
author name string
DiMauro S
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
Bonilla E
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
Lombes A
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
Shanske S
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
Minetti C
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
Moraes CT
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
publication date
1 August 1990
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
published in
Neurologic Clinics
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
volume
8
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
page(s)
483-506
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
cites work
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular defects in cytochrome oxidase in mitochondrial diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive neuronal degeneration of childhood (PNDC) with liver disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal inheritance of human mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identical mitochondrial DNA deletion in blood and muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in the cytochrome bc1 complex in mitochondrial diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Involvement of choroid plexus in mitochondrial encephalomyopathy (MELAS).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial encephalomyopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeting of nuclear-encoded proteins to the mitochondrial matrix: implications for human genetic defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and biochemical studies on cytochrome oxidase deficiencies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disorders of the pyruvate dehydrogenase complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations and neuromuscular disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930332-3
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%2FS0733-8619%2818%2930332-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0733-8619(18)30332-3
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
PubMed ID
2170831
1 reference
stated in
Europe PubMed Central
PubMed ID
2170831
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2170831%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit