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Journal Abstract Search

219 related items for PubMed ID: 10993457

  • 1. 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
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  • 2. A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.
    Govaerts PJ, De Ceulaer G, Daemers K, Verhoeven K, Van Camp G, Schatteman I, Verstreken M, Willems PJ, Somers T, Offeciers FE.
    Am J Otol; 1998 Nov; 19(6):718-23. PubMed ID: 9831143
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  • 4. [Audiologic analysis of a family with nonsyndromic genetic progressive sensorineural hearing loss].
    Ni D, Dan H, Mo J.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1999 Apr; 34(2):77-80. PubMed ID: 12764852
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  • 8. Audiometric analyses confirm a cochlear component, disproportional to age, in stapedial otosclerosis.
    Topsakal V, Fransen E, Schmerber S, Declau F, Yung M, Gordts F, Van Camp G, Van de Heyning P.
    Otol Neurotol; 2006 Sep; 27(6):781-7. PubMed ID: 16885785
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  • 9. 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
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  • 11. Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.
    Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ.
    J Assoc Res Otolaryngol; 2007 Mar; 8(1):1-7. PubMed ID: 17136632
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  • 13. Comparison of auditory steady-state responses and auditory brainstem responses in audiometric assessment of adults with sensorineural hearing loss.
    Lin YH, Ho HC, Wu HP.
    Auris Nasus Larynx; 2009 Apr; 36(2):140-5. PubMed ID: 18620826
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  • 15. Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.
    Weegerink NJ, Huygen PL, Schraders M, Kremer H, Pennings RJ, Kunst HP.
    Hear Res; 2011 Dec; 282(1-2):167-77. PubMed ID: 21893181
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  • 16. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
    Manolis EN, Eavey RD, Sangwatanaroj S, Halpin C, Rosenbaum S, Watkins H, Jarcho J, Seidman CE, Seidman JG.
    Am J Otol; 1999 Sep; 20(5):621-6. PubMed ID: 10503584
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  • 17. Audiologic phenotype of osteogenesis imperfecta: use in clinical differentiation.
    Swinnen FK, Dhooge IJ, Coucke PJ, D'Eufemia P, Zardo F, Garretsen TJ, Cremers CW, De Leenheer EM.
    Otol Neurotol; 2012 Feb; 33(2):115-22. PubMed ID: 22143304
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  • 18. Distribution of hearing loss characteristics in a clinical population.
    Margolis RH, Saly GL.
    Ear Hear; 2008 Aug; 29(4):524-32. PubMed ID: 18600134
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  • 20. 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; 109(9):1525-30. PubMed ID: 10499067
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