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Journal Abstract Search

161 related items for PubMed ID: 16261627

  • 21. 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]

  • 22. [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
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  • 23. 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 19; 11(10):744-8. PubMed ID: 14512963
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  • 24. 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 19; 120(12):2489-93. PubMed ID: 21046548
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  • 25. Identification of a novel Cochlin isoform in the perilymph: insights to Cochlin function and the pathogenesis of DFNA9.
    Ikezono T, Shindo S, Li L, Omori A, Ichinose S, Watanabe A, Kobayashi T, Pawankar R, Yagi T.
    Biochem Biophys Res Commun; 2004 Feb 06; 314(2):440-6. PubMed ID: 14733925
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  • 26. Massively Parallel Sequencing of a Chinese Family with DFNA9 Identified a Novel Missense Mutation in the LCCL Domain of COCH.
    Gu X, Su W, Tang M, Guo L, Zhao L, Li H.
    Neural Plast; 2016 Feb 06; 2016():5310192. PubMed ID: 28116169
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  • 28. 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 Feb 06; 12(2):77-84. PubMed ID: 17264471
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  • 29. 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 06; 26(5):926-33. PubMed ID: 16151339
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  • 31. A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 Phenotype.
    Smits JJ, van Beelen E, Weegerink NJD, Oostrik J, Huygen PLM, Beynon AJ, Lanting CP, Kunst HPM, Schraders M, Kremer H, de Vrieze E, Pennings RJE.
    Otol Neurotol; 2021 Apr 01; 42(4):e399-e407. PubMed ID: 33710989
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  • 32. First Report of Bilateral External Auditory Canal Cochlin Aggregates ("Cochlinomas") with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss and a Novel Genetic Variant in COCH Encoding Cochlin.
    Basu A, Boczek NJ, Robertson NG, Nasr SH, Jethanamest D, McPhail ED, Kurtin PJ, Dasari S, Butz M, Morton CC, Highsmith WE, Zhou F.
    Head Neck Pathol; 2020 Sep 01; 14(3):808-816. PubMed ID: 31493294
    [Abstract] [Full Text] [Related]

  • 33. Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9.
    Verdoodt D, van Wijk E, Broekman S, Venselaar H, Aben F, Sels L, De Backer E, Gommeren H, Szewczyk K, Van Camp G, Ponsaerts P, Van Rompaey V, de Vrieze E.
    Hear Res; 2024 Feb 01; 442():108947. PubMed ID: 38218018
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  • 34. 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
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  • 35. Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.
    Robertson NG, O'Malley JT, Ong CA, Giersch AB, Shen J, Stankovic KM, Morton CC.
    J Assoc Res Otolaryngol; 2014 Dec 01; 15(6):961-74. PubMed ID: 25049087
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  • 36. 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 Dec 01; 34(3):230-5. PubMed ID: 23374487
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  • 37. 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]

  • 38. 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
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  • 40. [Genotype--phenotype correlation limits in sensorineural hearing loss: case report of a three-year-old child with a bilateral cochleovestibular impairment and a molecular variant of the COCH gene].
    Montava M, Roman S, Sigaudy S, Marlin S, Nicollas R, Triglia JM.
    Rev Laryngol Otol Rhinol (Bord); 2012 Nov 01; 133(3):151-6. PubMed ID: 23590105
    [Abstract] [Full Text] [Related]

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