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PUBMED FOR HANDHELDS

Journal Abstract Search


133 related items for PubMed ID: 9639482

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  • 2. Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation.
    Tamagawa Y, Ishikawa K, Ishikawa K, Ishida T, Kitamura K, Makino S, Tsuru T, Ichimura K.
    Laryngoscope; 2002 Feb; 112(2):292-7. PubMed ID: 11889386
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  • 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
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  • 9. Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome.
    Griffith AJ, Gebarski SS, Shepard NT, Kileny PR.
    Arch Otolaryngol Head Neck Surg; 2000 Jul; 126(7):891-4. PubMed ID: 10889003
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  • 11. Visualization of endolymphatic hydrops and correlation with audio-vestibular functional testing in patients with definite Meniere's disease.
    Seo YJ, Kim J, Choi JY, Lee WS.
    Auris Nasus Larynx; 2013 Apr; 40(2):167-72. PubMed ID: 22867525
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  • 14. Investigation of endolymphatic hydrops by electrocochleography in patients with Cogan's syndrome.
    Benitez JT, Bojrab DI, Lubbers DE, Arsenault MD.
    Ear Nose Throat J; 1999 Dec; 78(12):929-33. PubMed ID: 10624058
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  • 15. Down syndrome: an electrophysiological and radiological profile.
    Saliba I, Sbeity S, El-Zir E, Yammine FG, Noun CT, Haddad A.
    Laryngoscope; 2014 Apr; 124(4):E141-7. PubMed ID: 24114773
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  • 16. Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy.
    Ceranić B, Luxon LM.
    J Neurol Neurosurg Psychiatry; 2004 Apr; 75(4):626-30. PubMed ID: 15026512
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  • 17. [Familial deafness showing hearing pattern of low-tone losses].
    Sasano T.
    Nihon Jibiinkoka Gakkai Kaiho; 1991 May; 94(5):667-77. PubMed ID: 1880639
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