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Journal Abstract Search

332 related items for PubMed ID: 18340555

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. Hearing loss in vestibular schwannomas: analysis of cochlear function by means of distortion-product otoacoustic emissions.
    Ferri GG, Modugno GC, Calbucci F, Ceroni AR, Pirodda A.
    Auris Nasus Larynx; 2009 Dec; 36(6):644-8. PubMed ID: 19419826
    [Abstract] [Full Text] [Related]

  • 23. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].
    Gallo-Terán J, Morales-Angulo C, del Castillo I, Villamar M, Moreno-Pelayo MA, García-Mantilla J, Moreno F.
    Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196
    [Abstract] [Full Text] [Related]

  • 24. Cochlear origin of hearing loss in MELAS syndrome.
    Sue CM, Lipsett LJ, Crimmins DS, Tsang CS, Boyages SC, Presgrave CM, Gibson WP, Byrne E, Morris JG.
    Ann Neurol; 1998 Mar; 43(3):350-9. PubMed ID: 9506552
    [Abstract] [Full Text] [Related]

  • 25. The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients.
    Rydzanicz M, Cywińska K, Wróbel M, Pollak A, Gawęcki W, Wojsyk-Banaszak I, Lechowicz U, Mueller-Malesińska M, Ołdak M, Płoski R, Skarżyński H, Szyfter K, Szyfter W.
    Mol Genet Metab; 2011 Mar; 104(1-2):153-9. PubMed ID: 21621438
    [Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene.
    Sue CM, Tanji K, Hadjigeorgiou G, Andreu AL, Nishino I, Krishna S, Bruno C, Hirano M, Shanske S, Bonilla E, Fischel-Ghodsian N, DiMauro S, Friedman R.
    Neurology; 1999 Jun 10; 52(9):1905-8. PubMed ID: 10371545
    [Abstract] [Full Text] [Related]

  • 28. [Mutations analysis in a pedigree with maternally inherited sensorineural hearing loss].
    Xu C, Zhang H, Zhang Y, Zhao S, Geng X, Shan Y, Shan X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 10; 22(2):125-8. PubMed ID: 15793769
    [Abstract] [Full Text] [Related]

  • 29. 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 10; 27(4):399-408. PubMed ID: 16825889
    [Abstract] [Full Text] [Related]

  • 30. [Measuring and analyzing of otoacoustic emission tests of a family with genetic progressive sensorineural hearing loss].
    Yu H, Ke XM, Yu DL, Li Q, Liu YH, Ding GY.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2000 Apr 10; 14(4):157-9. PubMed ID: 12541488
    [Abstract] [Full Text] [Related]

  • 31. [Distortion product otoacoustic emissions in sensorineural hearing loss].
    Skotnicka B, Hassmann-Poznańska E.
    Otolaryngol Pol; 1999 Apr 10; 53(6):693-8. PubMed ID: 10763321
    [Abstract] [Full Text] [Related]

  • 32. [Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].
    Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb 10; 19(1):64-7. PubMed ID: 11836692
    [Abstract] [Full Text] [Related]

  • 33. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
    [Abstract] [Full Text] [Related]

  • 34. A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment.
    Hutchin TP, Parker MJ, Young ID, Davis AC, Pulleyn LJ, Deeble J, Lench NJ, Markham AF, Mueller RF.
    J Med Genet; 2000 Sep 02; 37(9):692-4. PubMed ID: 10978361
    [Abstract] [Full Text] [Related]

  • 35. Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions.
    Santarelli R, Cama E, Scimemi P, Dal Monte E, Genovese E, Arslan E.
    Eur Arch Otorhinolaryngol; 2008 Jan 02; 265(1):43-51. PubMed ID: 17701047
    [Abstract] [Full Text] [Related]

  • 36. The mitochondrial A3243G mutation involves the peripheral vestibule as well as the cochlea.
    Iwasaki S, Egami N, Fujimoto C, Chihara Y, Ushio M, Kashio A, Yamasoba T.
    Laryngoscope; 2011 Aug 02; 121(8):1821-4. PubMed ID: 21792976
    [Abstract] [Full Text] [Related]

  • 37. The role of mitochondrial DNA mutations in hearing loss.
    Ding Y, Leng J, Fan F, Xia B, Xu P.
    Biochem Genet; 2013 Aug 02; 51(7-8):588-602. PubMed ID: 23605717
    [Abstract] [Full Text] [Related]

  • 38. Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss.
    Jiang H, Chen J, Li Y, Lin PF, He JG, Yang BB.
    Braz J Otorhinolaryngol; 2016 Aug 02; 82(4):391-6. PubMed ID: 26873147
    [Abstract] [Full Text] [Related]

  • 39. [Assessment of cochlear function with distortion products of otoacoustic emissions in acoustic neuroma].
    Oeken J.
    HNO; 1996 Dec 02; 44(12):677-84. PubMed ID: 9081952
    [Abstract] [Full Text] [Related]

  • 40. Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy.
    Ceranić B, Luxon LM.
    J Neurol Neurosurg Psychiatry; 2004 Apr 02; 75(4):626-30. PubMed ID: 15026512
    [Abstract] [Full Text] [Related]

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