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Journal Abstract Search

331 related items for PubMed ID: 11698812

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. Audiometric analysis of a Belgian family linked to the DFNA10 locus.
    Verstreken M, Declau F, Schatteman I, Van Velzen D, Verhoeven K, Van Camp G, Willems PJ, Kuhweide EW, Verhaert E, D'Haese P, Wuyts FL, Van de Heyning PH.
    Am J Otol; 2000 Sep; 21(5):675-81. PubMed ID: 10993457
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 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. Cochlear implantation in patients with bilateral Ménière's syndrome.
    Lustig LR, Yeagle J, Niparko JK, Minor LB.
    Otol Neurotol; 2003 May; 24(3):397-403. PubMed ID: 12806291
    [Abstract] [Full Text] [Related]

  • 9. Ménière's disease in children aged 4-7 years.
    Brantberg K, Duan M, Falahat B.
    Acta Otolaryngol; 2012 May; 132(5):505-9. PubMed ID: 22217217
    [Abstract] [Full Text] [Related]

  • 10. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug; 27(5):681-6. PubMed ID: 16868516
    [Abstract] [Full Text] [Related]

  • 11. [Cinical and genetic characteristics of familial Meniere's disease: three families report].
    Gao Y, Wang D, Wang H, Guan J, Lan L, Wu Z, Xie L, Yu L, Zhang S, Shan X, Wang Q.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 50(11):915-24. PubMed ID: 26887996
    [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 Nov; 12(2):77-84. PubMed ID: 17264471
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Gentamicin perfusion vestibular response and hearing loss.
    Light JP, Silverstein H, Jackson LE.
    Otol Neurotol; 2003 Mar; 24(2):294-8. PubMed ID: 12621347
    [Abstract] [Full Text] [Related]

  • 15. Correlation of Objective Audiometric and Caloric Function in Ménière's Disease.
    McMullen KP, Lin C, Harris MS, Adunka OF.
    Otolaryngol Head Neck Surg; 2017 May; 156(5):912-916. PubMed ID: 28168899
    [Abstract] [Full Text] [Related]

  • 16. Saccular dysfunction in Meniere's disease.
    de Waele C, Huy PT, Diard JP, Freyss G, Vidal PP.
    Am J Otol; 1999 Mar; 20(2):223-32. PubMed ID: 10100527
    [Abstract] [Full Text] [Related]

  • 17. Further characterization of the DFNA1 audiovestibular phenotype.
    Lalwani AK, Jackler RK, Sweetow RW, Lynch ED, Raventós H, Morrow J, King MC, León PE.
    Arch Otolaryngol Head Neck Surg; 1998 Jun; 124(6):699-702. PubMed ID: 9639482
    [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; 33(5):297-302. PubMed ID: 10890144
    [Abstract] [Full Text] [Related]

  • 19. Pure-tone and speech audiometry in patients with Menière's disease.
    Mateijsen DJ, Van Hengel PW, Van Huffelen WM, Wit HP, Albers FW.
    Clin Otolaryngol Allied Sci; 2001 Oct; 26(5):379-87. PubMed ID: 11678945
    [Abstract] [Full Text] [Related]

  • 20. 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]

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