(Q34442951)

2 August 2017

Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease (English)

1 reference

2 August 2017

5

Anna Lysakowski

1 reference

2 August 2017

Carmen Martín-Sierra

3

0 references

Teresa Requena

object named as

Teresa Requena

1

0 references

Jose A Lopez-Escamez

object named as

José A Lopez-Escamez

6

0 references

author name string

Sonia Cabrera

2

1 reference

PubMed ID

25305078

2 August 2017

Steven D Price

4

1 reference

2 August 2017

9 October 2014

1 reference

2 August 2017

Human Molecular Genetics

1 reference

2 August 2017

24

1 reference

2 August 2017

4

1 reference

2 August 2017

1119-1126

1 reference

PubMed ID

25305078

describes a project that uses

2 August 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4834881/fullTextXML

inferred from PubMed Central ID database lookup

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4834881/fullTextXML

inferred from PubMed Central ID database lookup

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Exome sequencing greatly expedites the progressive research of Mendelian diseases

6 July 2018

1 reference

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The promise of whole-exome sequencing in medical genetics

6 July 2018

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Improved exome prioritization of disease genes through cross-species phenotype comparison

6 July 2018

1 reference

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eXtasy: variant prioritization by genomic data fusion.

6 July 2018

1 reference

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Application of whole exome sequencing to identify disease-causing variants in inherited human diseases

6 July 2018

1 reference

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Absence of glial α-dystrobrevin causes abnormalities of the blood-brain barrier and progressive brain edema

6 July 2018

1 reference

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Exome sequencing and complex disease: practical aspects of rare variant association studies

6 July 2018

1 reference

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NIH Image to ImageJ: 25 years of image analysis

6 July 2018

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De novo mutations in human genetic disease

6 July 2018

1 reference

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Copy number variation detection and genotyping from exome sequence data

6 July 2018

1 reference

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Altered phenotype of the vestibular organ in GLAST-1 null mice.

6 July 2018

1 reference

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A systematic survey of loss-of-function variants in human protein-coding genes

6 July 2018

1 reference

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High prevalence of systemic autoimmune diseases in patients with Menière's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Molecular microdomains in a sensory terminal, the vestibular calyx ending

6 July 2018

1 reference

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Integration of transcriptomics, proteomics, and microRNA analyses reveals novel microRNA regulation of targets in the mammalian inner ear

6 July 2018

1 reference

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Genetic investigations of Meniere's disease

6 July 2018

1 reference

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Current epidemiology of Meniere's syndrome.

6 July 2018

1 reference

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Human Splicing Finder: an online bioinformatics tool to predict splicing signals

6 July 2018

1 reference

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Dystrobrevins in muscle and non-muscle tissues.

6 July 2018

1 reference

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Meniere's disease: prevalence of contralateral ear involvement

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Characterization and prediction of alternative splice sites

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Pathophysiology of Meniere's syndrome: are symptoms caused by endolymphatic hydrops?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

The AAO-HNS Committee on Hearing and Equilibrium guidelines for the diagnosis and evaluation of therapy in Menière's disease: have they been applied in the published literature of the last decade?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Improved splice site detection in Genie

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Dystrophin expression in the hair cells of the cochlea

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

The natural course of Meniere's disease.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

The effect of differential listening experience on the development of expressive and receptive language in children with bilateral cochlear implants

6 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

EuroQol 5D quality of life in Menière's disorder can be explained with symptoms and disabilities

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

Familial Ménière's disease: clinical and genetic aspects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

Familial clustering and genetic heterogeneity in Meniere's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

Genetic aspects of familial Ménière's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

Differential spatio-temporal expression of alpha-dystrobrevin-1 during mouse development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU524

Prevalence, associated factors, and comorbid conditions for Ménière's disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Vestibular migraine: diagnostic criteria.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Impact of bilaterality and headache on health-related quality of life in Meniere's disease.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

A Meniere's disease gene linked to chromosome 12p12.3.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4834881

Genetic and clinical heterogeneity in Meniere's disease

27 October 2018

1 reference

12 December 2020

Committee on Hearing and Equilibrium guidelines for the diagnosis and evaluation of therapy in Menière's disease. American Academy of Otolaryngology-Head and Neck Foundation, Inc

1 reference

12 December 2020

On genetic and environmental factors in Menière's disease

1 reference

12 December 2020

Characteristics of patients with unilateral and bilateral Ménière's disease

1 reference

12 December 2020

Familial Menière's disease: a genetic investigation

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDU524

1 reference

2 August 2017

1 reference

2 August 2017

1 reference

PubMed ID

25305078