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Autosomal dominant Kearns-Sayre syndrome.
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
title
Autosomal dominant Kearns-Sayre syndrome.
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
author name string
Leveille AS
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
Newell FW
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
publication date
1 February 1980
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
published in
Ophthalmology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
volume
87
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
page(s)
99-108
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
cites work
Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type I fiber hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
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%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive external ophthalmoplegia. Evidence for a generalised mitochondrial disease with a defect in pyruvate metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. II. Ultrastructure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissue
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Skeletal muscle disease with abnormal mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial progressive external ophthalmoplegia with abnormal muscle mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leukoencephalopathy in oculocraniosomatic neuromuscular disease with ragged-red fibers. Mitochondrial abnormalities demonstrated by computerized tomography
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Computed tomography in oculocraniosomatic disease (Kearns-Sayre syndrome)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myopathy with mitochondrial inclusion bodies: histological and metabolic studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electron cytochemistry of crystalline inclusions in human skeletal muscle mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2880%2935262-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0161-6420(80)35262-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
PubMed publication ID
7383548
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7383548
retrieved
16 June 2018
reference URL
http://europepmc.org/abstract/MED/7383548
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