(Q48266910)

10 February 2018

title

Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar system. (English)

1 reference

10 February 2018

main subject

Kearns-Sayre syndrome

1 reference

Tanji K

1

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10 February 2018

Vu TH

2

1 reference

10 February 2018

Schon EA

3

1 reference

10 February 2018

DiMauro S

4

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10 February 2018

Bonilla E

5

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10 February 2018

publication date

1 March 1999

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10 February 2018

published in

Annals of Neurology

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10 February 2018

volume

45

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10 February 2018

page(s)

377-383

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10 February 2018

issue

3

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10 February 2018

Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block

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1 reference

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Rearranged mitochondrial genomes are present in human oocytes

21 January 2018

1 reference

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Diseases of the mitochondrial DNA.

21 January 2018

1 reference

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Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

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Subunit arrangement in beef heart complex III.

21 January 2018

1 reference

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Paucity of deleted mitochondrial DNAs in brain regions of Huntington's disease patients

21 January 2018

1 reference

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Subacute necrotizing encephalomyelopathy in an infant

21 January 2018

1 reference

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Brain lesions of the Leigh-type distribution associated with a mitochondriopathy of Pearson's syndrome: light and electron microscopic study

21 January 2018

1 reference

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Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

New morphological approaches to the study of mitochondrial encephalomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Cerebellar outflow lesions: a comparison of movement deficits resulting from lesions at the levels of the cerebellum and thalamus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Duplications of mitochondrial DNA in mitochondrial myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?

21 January 2018

1 reference

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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

1 reference

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Cerebral infarction associated with Kearns-Sayre syndrome-related cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Efficient and specific amplification of identified partial duplications of human mitochondrial DNA by long PCR

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Immunocytochemical studies of cytochrome oxidase subunits in skeletal muscle of patients with partial cytochrome oxidase deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Antibodies against synthetic peptides reveal that the unidentified reading frame A6L, overlapping the ATPase 6 gene, is expressed in human mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Cytochemistry and immunocytochemistry of mitochondria in tissue sections

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Myoclonic epilepsy with ragged-red fibers (MERRF): an immunohistochemical study of the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

Behaviour of a population of partially duplicated mitochondrial DNA molecules in cell culture: segregation, maintenance and recombination dependent upon nuclear background

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199903%2945%3A3%3C377%3A%3AAID-ANA14%3E3.0.CO%3B2-M

10.1002/1531-8249(199903)45:3<377::AID-ANA14>3.0.CO;2-M

21 January 2018

Identifiers

DOI

1 reference

10 February 2018

release_uxvtbl7i2bdj3cfn5vw7ukshaq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/uxvtbl7i2bdj3cfn5vw7ukshaq

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

10072053

1 reference

10 February 2018