(Q30495451)

13 November 2017

Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy (English)

1 reference

hereditary optic neuropathy

13 November 2017

1 reference

Ceranić B

1

1 reference

PMCID

1739001

13 November 2017

Luxon LM

series ordinal

2

1 reference

PMCID

1739001

13 November 2017

language of work or name

English

0 references

publication date

1 April 2004

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

13 November 2017

1 reference

13 November 2017

75

1 reference

13 November 2017

4

1 reference

13 November 2017

626-630

1 reference

Hereditary deafness and phenotyping in humans

13 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

Consequences of neural asynchrony: a case of auditory neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

Further clinical and pathological observations on Leber's optic atrophy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

BAEP changes in Leber's hereditary optic atrophy: further confirmation of multisystem involvement

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1739001

A guide to the effective use of otoacoustic emissions

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15026512

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15026512

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Effect of contralateral auditory stimuli on active cochlear micro-mechanical properties in human subjects

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15026512

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.2003.017673

1 reference

13 November 2017

1 reference

13 November 2017

1 reference

PMCID

1739001