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150 related items for PubMed ID: 11843927

  • 1. Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family.
    Verhagen WI, Bom SJ, Fransen E, Van Camp G, Huygen PL, Theunissen EJ, Cremers CW.
    Clin Otolaryngol Allied Sci; 2001 Dec; 26(6):477-83. PubMed ID: 11843927
    [Abstract] [Full Text] [Related]

  • 2. Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9.
    Bom SJ, Kemperman MH, De Kok YJ, Huygen PL, Verhagen WI, Cremers FP, Cremers CW.
    Laryngoscope; 1999 Sep; 109(9):1525-30. PubMed ID: 10499067
    [Abstract] [Full Text] [Related]

  • 3. Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene.
    Verstreken M, Declau F, Wuyts FL, D'Haese P, Van Camp G, Fransen E, Van den Hauwe L, Buyle S, Smets RE, Feenstra L, Van der Stappen A, Van de Heyning PH.
    Otol Neurotol; 2001 Nov; 22(6):874-81. PubMed ID: 11698812
    [Abstract] [Full Text] [Related]

  • 4. Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo (DFNA9/COCH): longitudinal analyses in a belgian family.
    Lemaire FX, Feenstra L, Huygen PL, Fransen E, Devriendt K, Van Camp G, Vantrappen G, Cremers CW, Wackym PA, Koss JC.
    Otol Neurotol; 2003 Sep; 24(5):743-8. PubMed ID: 14501450
    [Abstract] [Full Text] [Related]

  • 5. A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.
    de Kok YJ, Bom SJ, Brunt TM, Kemperman MH, van Beusekom E, van der Velde-Visser SD, Robertson NG, Morton CC, Huygen PL, Verhagen WI, Brunner HG, Cremers CW, Cremers FP.
    Hum Mol Genet; 1999 Feb; 8(2):361-6. PubMed ID: 9931344
    [Abstract] [Full Text] [Related]

  • 6. Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH.
    Bom SJ, Kemperman MH, Huygen PL, Luijendijk MW, Cremers CW.
    Ann Otol Rhinol Laryngol; 2003 Mar; 112(3):280-6. PubMed ID: 12656423
    [Abstract] [Full Text] [Related]

  • 7. Audiometric, vestibular, and genetic aspects of a DFNA9 family with a G88E COCH mutation.
    Kemperman MH, De Leenheer EM, Huygen PL, van Duijnhoven G, Morton CC, Robertson NG, Cremers FP, Kremer H, Cremers CW.
    Otol Neurotol; 2005 Sep; 26(5):926-33. PubMed ID: 16151339
    [Abstract] [Full Text] [Related]

  • 8. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
    Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G.
    Eur J Hum Genet; 2003 Oct; 11(10):744-8. PubMed ID: 14512963
    [Abstract] [Full Text] [Related]

  • 9. Vertical corneal striae in families with autosomal dominant hearing loss: DFNA9/COCH.
    Bischoff AM, Pauw RJ, Huygen PL, Aandekerk AL, Kremer H, Cremers CW, Cruysberg JR.
    Am J Ophthalmol; 2007 May; 143(5):847-852. PubMed ID: 17368553
    [Abstract] [Full Text] [Related]

  • 10. Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriers.
    Bischoff AM, Huygen PL, Kemperman MH, Pennings RJ, Bom SJ, Verhagen WI, Admiraal RJ, Kremer H, Cremers CW.
    Otol Neurotol; 2005 Sep; 26(5):918-25. PubMed ID: 16151338
    [Abstract] [Full Text] [Related]

  • 11. Phenotype description of a novel DFNA9/COCH mutation, I109T.
    Pauw RJ, Huygen PL, Collin RW, Cruysberg JR, Hoefsloot LH, Kremer H, Cremers CW.
    Ann Otol Rhinol Laryngol; 2007 May; 116(5):349-57. PubMed ID: 17561763
    [Abstract] [Full Text] [Related]

  • 12. Clinical characteristics of a Dutch DFNA9 family with a novel COCH mutation, G87W.
    Pauw RJ, Collin RW, Huygen PL, Hoefsloot LH, Kremer H, Cremers CW.
    Audiol Neurootol; 2007 May; 12(2):77-84. PubMed ID: 17264471
    [Abstract] [Full Text] [Related]

  • 13. A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation.
    Fransen E, Verstreken M, Bom SJ, Lemaire F, Kemperman MH, De Kok YJ, Wuyts FL, Verhagen WI, Huygen PL, McGuirt WT, Smith RJ, Van Maldergem LV, Declau F, Cremers CW, Van De Heyning PH, Cremers FP, Van Camp G.
    J Med Genet; 2001 Jan; 38(1):61-5. PubMed ID: 11332404
    [No Abstract] [Full Text] [Related]

  • 14. The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
    Fransen E, Van Camp G.
    Br J Audiol; 1999 Oct; 33(5):297-302. PubMed ID: 10890144
    [Abstract] [Full Text] [Related]

  • 15. Distinct vestibular phenotypes in DFNA9 families with COCH variants.
    Kim BJ, Kim AR, Han KH, Rah YC, Hyun J, Ra BS, Koo JW, Choi BY.
    Eur Arch Otorhinolaryngol; 2016 Oct; 273(10):2993-3002. PubMed ID: 26758463
    [Abstract] [Full Text] [Related]

  • 16. High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.
    Fransen E, Verstreken M, Verhagen WI, Wuyts FL, Huygen PL, D'Haese P, Robertson NG, Morton CC, McGuirt WT, Smith RJ, Declau F, Van de Heyning PH, Van Camp G.
    Hum Mol Genet; 1999 Aug; 8(8):1425-9. PubMed ID: 10400989
    [Abstract] [Full Text] [Related]

  • 17. [From gene to disease; a progressive cochlear-vestibular dysfunction with onset in middle-age (DFNA9)].
    Cremers CW, Kemperman MH, Bom SJ, Huygen PL, Verhagen WI, Kremer JM.
    Ned Tijdschr Geneeskd; 2005 Nov 19; 149(47):2619-21. PubMed ID: 16355574
    [Abstract] [Full Text] [Related]

  • 18. Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9).
    Verhagen WI, Bom SJ, Huygen PL, Fransen E, Van Camp G, Cremers CW.
    Arch Neurol; 2000 Jul 19; 57(7):1045-7. PubMed ID: 10891988
    [Abstract] [Full Text] [Related]

  • 19. A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene.
    JanssensdeVarebeke S, Topsakal V, Van Camp G, Van Rompaey V.
    Eur Arch Otorhinolaryngol; 2019 May 19; 276(5):1251-1262. PubMed ID: 30806805
    [Abstract] [Full Text] [Related]

  • 20. Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion.
    Jung J, Kim HS, Lee MG, Yang EJ, Choi JY.
    Hum Mutat; 2015 Dec 19; 36(12):1168-75. PubMed ID: 26256111
    [Abstract] [Full Text] [Related]

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