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Journal Abstract Search

213 related items for PubMed ID: 10400989

  • 1. 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]

  • 2. 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]

  • 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. 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]

  • 5. 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]

  • 6. 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]

  • 7. 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]

  • 8. 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; 12(1):75-8. PubMed ID: 14704763
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. A Meniere's disease gene linked to chromosome 12p12.3.
    Klar J, Frykholm C, Friberg U, Dahl N.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Jul 05; 141B(5):463-7. PubMed ID: 16741942
    [Abstract] [Full Text] [Related]

  • 11. 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 05; 26(5):926-33. PubMed ID: 16151339
    [Abstract] [Full Text] [Related]

  • 12. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug 05; 27(5):681-6. PubMed ID: 16868516
    [Abstract] [Full Text] [Related]

  • 13. [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 05; 50(11):915-24. PubMed ID: 26887996
    [Abstract] [Full Text] [Related]

  • 14. Diagnostic criteria for Menière's disease.
    Lopez-Escamez JA, Carey J, Chung WH, Goebel JA, Magnusson M, Mandalà M, Newman-Toker DE, Strupp M, Suzuki M, Trabalzini F, Bisdorff A, Classification Committee of the Barany Society, Japan Society for Equilibrium Research, European Academy of Otology and Neurotology (EAONO), Equilibrium Committee of the American Academy of Otolaryngology-Head and Neck Surgery (AAO-HNS), Korean Balance Society.
    J Vestib Res; 2015 Nov 05; 25(1):1-7. PubMed ID: 25882471
    [Abstract] [Full Text] [Related]

  • 15. A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.
    Hildebrand MS, Gandolfo L, Shearer AE, Webster JA, Jensen M, Kimberling WJ, Stephan D, Huygen PL, Smith RJ, Bahlo M.
    Laryngoscope; 2010 Dec 05; 120(12):2489-93. PubMed ID: 21046548
    [Abstract] [Full Text] [Related]

  • 16. The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
    Fransen E, Van Camp G.
    Br J Audiol; 1999 Oct 05; 33(5):297-302. PubMed ID: 10890144
    [Abstract] [Full Text] [Related]

  • 17. Familial clustering of migraine, episodic vertigo, and Ménière's disease.
    Cha YH, Kane MJ, Baloh RW.
    Otol Neurotol; 2008 Jan 05; 29(1):93-6. PubMed ID: 18046258
    [Abstract] [Full Text] [Related]

  • 18. [Diagnostic criteria for Menière's disease according to the Classification Committee of the Bárány Society].
    Lopez-Escamez JA, Carey J, Chung WH, Goebel JA, Magnusson M, Mandalà M, Newman-Toker DE, Strupp M, Suzuki M, Trabalzini F, Bisdorff A.
    HNO; 2017 Nov 05; 65(11):887-893. PubMed ID: 28770282
    [Abstract] [Full Text] [Related]

  • 19. 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 05; 143(5):847-852. PubMed ID: 17368553
    [Abstract] [Full Text] [Related]

  • 20. 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 05; 12(2):77-84. PubMed ID: 17264471
    [Abstract] [Full Text] [Related]

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