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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

232 related items for PubMed ID: 23013294

  • 1.
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  • 2. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
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  • 3. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
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  • 4. Clinical and audiological follow up of a family with the 8363G>A mutation in the mitochondrial DNA.
    DiFabio R, Santorelli FM, Nola G, Cricchi F, Masi R, Ingrosso A, Fattori F, Carrozzo R, Vanacore N, Pierelli F, Ralli G, Casali C.
    Neuromuscul Disord; 2009 Apr; 19(4):291-6. PubMed ID: 19233651
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  • 6. [Hearing loss in triplets].
    Willenborg KM, Götz F, Lenarz T, Lesinski-Schiedat A.
    Laryngorhinootologie; 2010 Aug; 89(8):485-8. PubMed ID: 20387194
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  • 8. Audiometric characteristics of a Dutch family with Muckle-Wells syndrome.
    Weegerink NJ, Schraders M, Leijendeckers J, Slieker K, Huygen PL, Hoefsloot L, Oostrik J, Pennings RJ, Simon A, Snik A, Kremer H, Kunst HP.
    Hear Res; 2011 Dec; 282(1-2):243-51. PubMed ID: 21810457
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  • 9. Auditory neuropathy characteristics in children with cochlear nerve deficiency.
    Buchman CA, Roush PA, Teagle HF, Brown CJ, Zdanski CJ, Grose JH.
    Ear Hear; 2006 Aug; 27(4):399-408. PubMed ID: 16825889
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  • 10. [Clinical and audiological findings in children with auditory neuropathy].
    Shehata-Dieler W, Völter C, Hildmann A, Hildmann H, Helms J.
    Laryngorhinootologie; 2007 Jan; 86(1):15-21. PubMed ID: 17283495
    [Abstract] [Full Text] [Related]

  • 11. Hearing loss associated with enlarged vestibular aqueduct and Mondini dysplasia is caused by splice-site mutation in the PDS gene.
    Yang JJ, Tsai CC, Hsu HM, Shiao JY, Su CC, Li SY.
    Hear Res; 2005 Jan; 199(1-2):22-30. PubMed ID: 15574297
    [Abstract] [Full Text] [Related]

  • 12. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S.
    Ann Otol Rhinol Laryngol; 2005 Feb; 114(2):153-60. PubMed ID: 15757197
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  • 15. Despite a lack of otoacoustic emission, word recognition is not seriously influenced in a TECTA DFNA8/12 family.
    Ramsebner R, Koenighofer M, Parzefall T, Lucas T, Schoefer C, Frei K.
    Int J Pediatr Otorhinolaryngol; 2014 May; 78(5):837-42. PubMed ID: 24636747
    [Abstract] [Full Text] [Related]

  • 16. Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.
    Huang T, Santarelli R, Starr A.
    Brain Res; 2009 Dec 01; 1300():97-104. PubMed ID: 19733158
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  • 17. X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care.
    Stanton SG, Griffin A, Stockley TL, Brown C, Young TL, Benteau T, Abdelfatah N.
    Am J Audiol; 2014 Jun 01; 23(2):190-200. PubMed ID: 24687041
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  • 19. 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 01; 8(1):1-7. PubMed ID: 17136632
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  • 20. Audiological characteristics of some affected members of a Dutch DFNA13/COL11A2 family.
    De Leenheer EM, Bosman AJ, Kunst HP, Huygen PL, Cremers CW.
    Ann Otol Rhinol Laryngol; 2004 Nov 01; 113(11):922-9. PubMed ID: 15562903
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