Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

DPOAEs and vestibular function in different types of autosomal-dominant non-syndromal hearing impairment.

Auris, nasus, larynx - 1 Jan 2002

Oeken Jens, Stumpf Robert, Bootz Friedrich

Abstract excerpt

BACKGROUND/OBJECTIVE: The application of distortion-product otoacoustic emissions (DPOAE) could be advantageous in the early diagnostic of descendants of families with autosomal-dominant non-syndromal hearing impairment (ADNSHI). PATIENTS/METHODS: DP-grams of 58 affected persons of 21 families wi...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Aged
Share to Hearing Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Otoacoustic Emissions, Spontaneous

Share to Pedigree

Share to Severity of Illness Index

Share to Syndrome

Share to Vestibule, Labyrinth

Source

Identifiers

PMID: 11772487
DOI: 10.1016/s0385-8146(01)00119-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11772487-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

DPOAEs and vestibular function in different types of autosomal-dominant non-syndromal hearing impairment.PMID 11772487Read ↗

Features of autosomal recessive non-syndromic hearing impairment: a review to serve as a reference.Semantic proximity Read ↗

Distortion-product otoacoustic emissions at ultra-high frequencies in parents of individuals with autosomal recessive hearing loss.Semantic proximity Read ↗

Audiometric patterns of genetic non-syndromal sensorineural hearing loss.Semantic proximity Read ↗

The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.Semantic proximity Read ↗

Phenotypic characterization of DFNA24: prelingual progressive sensorineural hearing impairment.Semantic proximity Read ↗

Audiometric characteristics of two Dutch families with non-ocular Stickler syndrome (COL11A2).Semantic proximity Read ↗

[Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss].Semantic proximity Read ↗

The large Chinese family with Y-linked hearing loss revisited: clinical investigation.Semantic proximity Read ↗

[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances].Semantic proximity Read ↗

A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells.Semantic proximity Read ↗

A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13.Semantic proximity Read ↗

Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.