BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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; 12(2):77-84. PubMed ID: 17264471
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.