About: Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia

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About: Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 1985

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 1985 (uk) article scientifique publié en 1985 (fr) im August 1985 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 1985 (ast) scientific article published on 01 August 1985 (en)
publication date	wds:Q70101862-6A331595-11C3-4557-9523-0B3F03534C22
publication date	1985-08-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q70101862-5C41488D-8366-42E8-9861-7D54D25AC6BA wds:Q70101862-7D967662-DD24-4656-812B-9630D7019A0B wds:Q70101862-80BC1119-95B9-442E-AF62-C1102E87B510 wds:Q70101862-D803FB9F-640D-49DB-B822-A11425C14B84 wds:Q70101862-F295AECA-E1B8-4EAC-A3D5-78D6D6220BC3
author name string	D M Turnbull M A Johnson N E Cartlidge H S Sherratt D J Dick
rdfs:label	Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia (en) Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia (nl)
skos:prefLabel	Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia (en) Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia (nl)
name	Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia (en) Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia (nl)
title	wds:Q70101862-3D859762-2960-4DE4-99EA-97FE27E59873
title	Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia (en)
page(s)	wds:Q70101862-2D5DD343-C191-4A43-9002-0FA77284C551
page(s)	93-100
instance of	wds:Q70101862-86F57DCC-B6BB-461C-BA35-01BBF5BB4299
instance of	scholarly article
main subject	wds:Q70101862-1AECAF49-DF58-420F-863D-EBF6A6A4A1A0
main subject	chronic progressive external ophthalmoplegia
PubMed ID	wds:Q70101862-A82A1B75-0859-4003-81DD-D605E0C0F9D6
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2995595
PubMed ID	2995595
published in	wds:Q70101862-6295A786-6B26-435F-B060-54F898530843
published in	Journal of the Neurological Sciences
issue	wds:Q70101862-E122A7CA-6C0A-47B3-9265-E1825B62FD59
volume	wds:Q70101862-42627412-40B8-40CE-AB7F-66D2CACCA164
issue	1
volume	70
DOI	wds:Q70101862-0DDA26DF-E068-41DE-9A9F-BA6313F9A484
DOI	http://dx.doi.org/10.1016/0022-510X(85)90191-1
DOI	10.1016/0022-510X(85)90191-1
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70101862
is cites work of	Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study. Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome. Isolation and characterization of mitochondria from human B lymphoblastoid cell lines Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder Screening for mitochondrial cytopathies: the sub-anaerobic threshold exercise test (SATET). Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions: an immunocytochemical study Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency
is cites work of	wds:Q41613950-BF72D70B-70EA-40C7-A966-E51B2867B9EE wds:Q73987203-236344E0-61E0-4619-B30C-0FBA4CE50747 wds:Q28280475-F19B7435-26D3-4E3C-806F-47D82EA97E85 wds:Q33681824-140253C8-3860-4274-B330-15ACB41531D4 wds:Q33627799-EE41F117-E31F-46D9-84EC-E2F4857EB24B wds:Q34323823-2D4F6256-A83C-4615-A86C-412B8BACFB23 wds:Q35816863-B6B73858-9AFC-41E3-86DD-F04FE3D3067E wds:Q50550831-C883941E-A987-4F2F-9D27-5F32C38B62D1 wds:Q68258744-81BBE037-3233-421B-9ACE-A55CBEBBB536 wds:Q42588888-1D2BB59D-612A-4326-91AE-12400C0DD0E0

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