(Q50518910)

English

Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNAIle 4269 mutation): histochemical, immunohistochemical, and ultrastructural study

scientific article published on August 1, 1995

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNAIle 4269 mutation): histochemical, immunohistochemical, and ultrastructural study (English)

reason for preferred rank

most precise value

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA(Ile) 4269 mutation): histochemical, immunohistochemical, and ultrastructural study (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

immunohistochemistry

1 reference

based on heuristic

inferred from title

mitochondrial encephalomyopathy

1 reference

based on heuristic

inferred from title

author name string

M. Kaido

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

H. Fujimura

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

M. Taniike

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

H. Yoshikawa

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

K. Toyooka

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

S. Yorifuji

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

K. Inui

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

S. Okada

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

M. Sparaco

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

T. Yanagihara

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7595643

3 June 2024

publication date

1 August 1995

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

full work available at URL

https://doi.org/10.1016/0022-510x(95)00111-e

online access status

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7595643

3 June 2024

https://api.elsevier.com/content/article/PII:0022510X9500111E?httpAccept=text/xml

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

https://api.elsevier.com/content/article/PII:0022510X9500111E?httpAccept=text/plain

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Journal of the Neurological Sciences

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

131

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

170-176

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

Cerebral spongy degeneration of infancy. A biochemical and ultrastructural study of affected twins.

1

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study

2

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Mitochondrial myopathy and cardiomyopathy with neurodegenerative features and multiple brain infarcts.

3

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Spongiform encephalopathy with chronic progressive external ophthalmoplegia. Central ophthalmoplegia mimicking ocular myopathy

4

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

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

6

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Spongy degeneration of the CNS: an instance of the rare juvenile form

7

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

8

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia.

9

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency

10

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Subacute necrotizing encephalomyelopathy. A review and a study of two families

11

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study

12

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy

13

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissue

14

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy

15

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Skeletal muscle pathology in chronic progressive external ophthalmoplegia with ragged-red fibers

17

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Decreased activities in mitochondrial inner membrane electron transport system in muscle from patients with Kearns-Sayre syndrome

18

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient

19

1 reference

10.1016/0022-510X(95)00111-E

https://api.crossref.org/works/10.1016/0022-510X(95)00111-E

3 June 2024

Identifiers

10.1016/0022-510X(95)00111-E

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7595643

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50518910&oldid=2171258232"