Vestibular Deterioration Precedes Hearing Deterioration in the P51S COCH Mutation (DFNA9): An Analysis in 74 Mutation Carriers-Reference-Cited by-同舟云学术

Vestibular Deterioration Precedes Hearing Deterioration in the P51S COCH Mutation (DFNA9): An Analysis in 74 Mutation Carriers

Published:2005-09 Issue:5 Volume:26 Page:918-925
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Bischoff Anne M. L. C,Huygen Patrick L. M,Kemperman Martijn H,Pennings Ronald J. E,Bom Steven J. H,Verhagen Wim I. M,Admiraal Ronald J. C,Kremer Hannie,Cremers Cor W. R. J

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference24 articles.

1. Familial progressive vestibulocochlear dysfunction.;Verhagen;Arch Neurol,1988

2. A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.;Manolis;Hum Mol Genet,1996

3. Mapping and characterization of a novel cochlear gene in human and in mouse: A positional candidate gene for a deafness disorder, DFNA9.;Robertson;Genomics,1997

4. A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.;de Kok;Hum Mol Genet,1999

5. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.;Robertson;Nat Genet,1998

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1. Interaural and sex differences in the natural evolution of hearing levels in pre-symptomatic and symptomatic carriers of the p.Pro51Ser variant in the COCH gene;Scientific Reports;2024-01-02

2. Association of Bilateral Vestibulopathy With and Without Hearing Loss With Cognitive-Motor Interference;JAMA Otolaryngology–Head & Neck Surgery;2023-08-01

3. Accelerated Cognitive Decline Associated With Hearing Loss and Bilateral Vestibulopathy: Insights From a Prospective Cross-Sectional Study Using the Repeatable Battery for the Assessment of Neuropsychological Status Adjusted for the Hearing Impaired in the DFNA9 Population;Ear & Hearing;2022-12-20

4. Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis;Biomolecules;2022-01-27

5. Genotype-Phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9) Part II: A Prospective Cross-Sectional Study of the Vestibular Phenotype in 111 Carriers;Ear & Hearing;2021-10-22