(Q35666517)

9 August 2017

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title

The MELAS syndrome. Review of the literature: the role of the otologist (English)

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9 August 2017

Karkos PD

1

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9 August 2017

Waldron M

series ordinal

2

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9 August 2017

Johnson IJ

series ordinal

3

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9 August 2017

publication date

1 February 2004

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9 August 2017

published in

Clinical Otolaryngology

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9 August 2017

volume

29

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9 August 2017

issue

1

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9 August 2017

page(s)

1-4

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Histopathology and molecular genetics of hearing loss in the human

9 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Paternal inheritance of mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Genes and syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Mitochondrial encephalomyopathy: a rare genetic cause of sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

The otolaryngological manifestations of mitochondrial disease and the risk of neurodegeneration with infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

The spectrum of hearing loss due to mitochondrial DNA defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Melas: an original case and clinical criteria for diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Reversible alexia, mitochondrial myopathy, and lactic acidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

Cochlear implantation in a profoundly deaf patient with MELAS syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2273.2004.00769.X

10.1111/J.1365-2273.2004.00769.X

21 January 2018

Identifiers

DOI

1 reference

release_evdns6oikfbvvowz44but52zl4

9 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/evdns6oikfbvvowz44but52zl4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference