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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 10993457

  • 61. Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions.
    Kunst H, Marres H, Huygen P, Van Camp G, Joosten F, Cremers C.
    Audiology; 1999; 38(3):165-73. PubMed ID: 10437687
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  • 66. [Assessment of social hearing with a questionnaire in relation to average hearing loss].
    Dieroff HG, Meissner W.
    Laryngol Rhinol Otol (Stuttg); 1987 Jun; 66(6):338-40. PubMed ID: 3626718
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  • 67. Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis.
    Oonk AM, Leijendeckers JM, Lammers EM, Weegerink NJ, Oostrik J, Beynon AJ, Huygen PL, Kunst HP, Kremer H, Snik AF, Pennings RJ.
    Hear Res; 2013 May; 299():88-98. PubMed ID: 23340379
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  • 70. 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
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  • 80. Acute idiopathic sensorineural hearing impairment at frequency exceeding 8 kHz.
    Sakata T, Ueno T, Takase H, Shiraishi K, Nakagawa T.
    Acta Otolaryngol; 2010 Oct; 130(10):1141-6. PubMed ID: 20297929
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