(Q48971174)

17 February 2018

title

Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies. (English)

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17 February 2018

sensorineural hearing loss

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Zwirner P

1

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17 February 2018

Wilichowski E

series ordinal

2

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17 February 2018

language of work or name

English

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publication date

1 March 2001

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17 February 2018

number of pages

7

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based on heuristic

inferred from page(s)

published in

The Laryngoscope

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17 February 2018

volume

111

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17 February 2018

issue

3

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17 February 2018

page(s)

515-521

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17 February 2018

Diseases of the mitochondrial DNA.

cites work

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

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/10.1097%2F00005537-200103000-00024

Biogenesis of mitochondria and genetics of mitochondrial defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Cochlear origin of hearing loss in MELAS syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns-Sayre/MELAS overlap syndrome and A3243G mtDNA mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Kearns-sayre syndrome. Two clinico-pathological cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Mitochondrial encephalomyopathies: a correlation between neuropathological findings and defects in mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Neuropathology in Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Development and degeneration of hearing in the C57/b16 mouse: relation of electrophysiologic responses from the round window and cochlear nucleus to cochlear anatomy and behavioral responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Positive endocochlear potential: mechanism of production by marginal cells of stria vascularis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Distribution of immunoreactive Na+,K+-ATPase in gerbil cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

21 January 2018

Mitochondrial medicine

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

Histopathologic features of the inner ear associated with Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00005537-200103000-00024

10.1097/00005537-200103000-00024

21 January 2018

Identifiers

DOI

1 reference

17 February 2018

1 reference

17 February 2018