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Journal Abstract Search

154 related items for PubMed ID: 16151339

  • 1. 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]

  • 2. 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 Sep; 12(2):77-84. PubMed ID: 17264471
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
    Pauw RJ, Huygen PL, Colditz GM, Cremers CW.
    Ann Otol Rhinol Laryngol; 2011 Jun; 120(6):414-21. PubMed ID: 21774451
    [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. Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder.
    Jones SM, Robertson NG, Given S, Giersch AB, Liberman MC, Morton CC.
    Hear Res; 2011 Feb; 272(1-2):42-8. PubMed ID: 21073934
    [Abstract] [Full Text] [Related]

  • 8. Detailed hearing and vestibular profiles in the patients with COCH mutations.
    Tsukada K, Ichinose A, Miyagawa M, Mori K, Hattori M, Nishio SY, Naito Y, Kitajiri S, Usami S.
    Ann Otol Rhinol Laryngol; 2015 May; 124 Suppl 1():100S-10S. PubMed ID: 25780252
    [Abstract] [Full Text] [Related]

  • 9. Genotype-phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9): Part I-A Cross-sectional Study of Hearing Function in 111 Carriers.
    JanssensdeVarebeke SPF, Moyaert J, Fransen E, Bulen B, Neesen C, Devroye K, van de Berg R, Pennings RJE, Topsakal V, Vanderveken O, Van Camp G, Van Rompaey V.
    Ear Hear; 2015 May; 42(6):1508-1524. PubMed ID: 34369416
    [Abstract] [Full Text] [Related]

  • 10. A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.
    Robertson NG, Jones SM, Sivakumaran TA, Giersch AB, Jurado SA, Call LM, Miller CE, Maison SF, Liberman MC, Morton CC.
    Hum Mol Genet; 2008 Nov 01; 17(21):3426-34. PubMed ID: 18697796
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 24(5):743-8. PubMed ID: 14501450
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 276(5):1251-1262. PubMed ID: 30806805
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 22(6):874-81. PubMed ID: 11698812
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 26(6):477-83. PubMed ID: 11843927
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 143(5):847-852. PubMed ID: 17368553
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 38(1):61-5. PubMed ID: 11332404
    [No Abstract] [Full Text] [Related]

  • 17. 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.
    JanssensdeVarebeke SPF, Moyaert J, Fransen E, Bulen B, Neesen C, Devroye K, van de Berg R, Pennings RJE, Topsakal V, Vanderveken O, Van Camp G, Van Rompaey V.
    Ear Hear; 2001 Jan 01; 42(6):1525-1543. PubMed ID: 34369417
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 109(9):1525-30. PubMed ID: 10499067
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 8(2):361-6. PubMed ID: 9931344
    [Abstract] [Full Text] [Related]

  • 20. Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.
    Robertson NG, Cremers CW, Huygen PL, Ikezono T, Krastins B, Kremer H, Kuo SF, Liberman MC, Merchant SN, Miller CE, Nadol JB, Sarracino DA, Verhagen WI, Morton CC.
    Hum Mol Genet; 2006 Apr 01; 15(7):1071-85. PubMed ID: 16481359
    [Abstract] [Full Text] [Related]

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