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Journal Abstract Search

585 related items for PubMed ID: 14512963

  • 1. 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]

  • 2. [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]

  • 3. 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 19; 143(5):847-852. PubMed ID: 17368553
    [Abstract] [Full Text] [Related]

  • 4. Absence of COCH mutations in patients with Meniere disease.
    Sanchez E, López-Escámez JA, López-Nevot MA, López-Nevot A, Cortes R, Martin J.
    Eur J Hum Genet; 2004 Jan 19; 12(1):75-8. PubMed ID: 14704763
    [Abstract] [Full Text] [Related]

  • 5. 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 19; 8(8):1425-9. PubMed ID: 10400989
    [Abstract] [Full Text] [Related]

  • 6. 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 19; 22(6):874-81. PubMed ID: 11698812
    [Abstract] [Full Text] [Related]

  • 7. 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 19; 109(9):1525-30. PubMed ID: 10499067
    [Abstract] [Full Text] [Related]

  • 8. Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families.
    Kamarinos M, McGill J, Lynch M, Dahl H.
    Hum Mutat; 2001 Apr 19; 17(4):351. PubMed ID: 11295836
    [Abstract] [Full Text] [Related]

  • 9. 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 19; 24(5):743-8. PubMed ID: 14501450
    [Abstract] [Full Text] [Related]

  • 10. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 19; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 11. 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 19; 273(10):2993-3002. PubMed ID: 26758463
    [Abstract] [Full Text] [Related]

  • 12. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.
    Robertson NG, Lu L, Heller S, Merchant SN, Eavey RD, McKenna M, Nadol JB, Miyamoto RT, Linthicum FH, Lubianca Neto JF, Hudspeth AJ, Seidman CE, Morton CC, Seidman JG.
    Nat Genet; 1998 Nov 19; 20(3):299-303. PubMed ID: 9806553
    [Abstract] [Full Text] [Related]

  • 13. Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus.
    Gallant E, Francey L, Fetting H, Kaur M, Hakonarson H, Clark D, Devoto M, Krantz ID.
    Am J Otolaryngol; 2013 Nov 19; 34(3):230-5. PubMed ID: 23374487
    [Abstract] [Full Text] [Related]

  • 14. Inheritance of Meniere's disease in the Finnish population.
    Klockars T, Kentala E.
    Arch Otolaryngol Head Neck Surg; 2007 Jan 19; 133(1):73-7. PubMed ID: 17224529
    [Abstract] [Full Text] [Related]

  • 15. 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 19; 8(2):361-6. PubMed ID: 9931344
    [Abstract] [Full Text] [Related]

  • 16. 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 19; 26(6):477-83. PubMed ID: 11843927
    [Abstract] [Full Text] [Related]

  • 17. Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.
    Wagatsuma M, Kitoh R, Suzuki H, Fukuoka H, Takumi Y, Usami S.
    Clin Genet; 2007 Oct 19; 72(4):339-44. PubMed ID: 17850630
    [Abstract] [Full Text] [Related]

  • 18. The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
    Fransen E, Van Camp G.
    Br J Audiol; 1999 Oct 19; 33(5):297-302. PubMed ID: 10890144
    [Abstract] [Full Text] [Related]

  • 19. 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 19; 124 Suppl 1():100S-10S. PubMed ID: 25780252
    [Abstract] [Full Text] [Related]

  • 20. Evaluation of retrosigmoid vestibular neurectomy for intractable vertigo in Ménière's disease: an interdisciplinary review.
    Li CS, Lai JT.
    Acta Neurochir (Wien); 2008 Jul 19; 150(7):655-61; discussion 661. PubMed ID: 18536995
    [Abstract] [Full Text] [Related]

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