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149 related items for PubMed ID: 15757197

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. [Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss].
    Xing G, Bu X, Yan M, Lu L, Yang S.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 35(2):98-101. PubMed ID: 12768662
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S.
    Laryngoscope; 2004 Jun; 114(6):1085-91. PubMed ID: 15179218
    [Abstract] [Full Text] [Related]

  • 5. Audiological and radiological characteristics of a family with T961G mitochondrial mutation.
    Turchetta R, Mazzei F, Celani T, Cammeresi MG, Orlando MP, Altissimi G, de Vincentiis C, D'Ambrosio F, Messineo D, Ferraris A, Cianfrone G.
    Int J Audiol; 2012 Dec; 51(12):870-9. PubMed ID: 23013294
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)].
    Morales Angulo C, Gallo Terán J, del Castillo I, Moreno Pelayo MA, García-Mantilla J, Moreno Herrero F.
    Acta Otorrinolaringol Esp; 2002 Nov 02; 53(9):641-8. PubMed ID: 12584878
    [Abstract] [Full Text] [Related]

  • 8. [Non-syndromic familial hearing impairment transmitted by mitochondrial inheritance].
    Morales Angulo C, Del Castillo I, Sarduy M, Villamar M, Mazón A, Moreno F.
    Acta Otorrinolaringol Esp; 1999 Mar 02; 50(2):93-9. PubMed ID: 10217681
    [Abstract] [Full Text] [Related]

  • 9. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.
    Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 10; 340(2):583-8. PubMed ID: 16380089
    [Abstract] [Full Text] [Related]

  • 10. [Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].
    YANG AF, ZHENG J, LV JX, GUAN MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr 10; 28(2):165-71. PubMed ID: 21462128
    [Abstract] [Full Text] [Related]

  • 11. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
    Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1244-51. PubMed ID: 15708009
    [Abstract] [Full Text] [Related]

  • 12. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep 25; 113(9):1623-9. PubMed ID: 12972945
    [Abstract] [Full Text] [Related]

  • 13. [Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA].
    Gallo-Terán J, Morales-Angulo C, del Castillo I, Moreno-Pelayo MA, Mazón A, Moreno F.
    Med Clin (Barc); 2003 Jul 12; 121(6):216-8. PubMed ID: 12882732
    [Abstract] [Full Text] [Related]

  • 14. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation.
    Tono T, Ushisako Y, Kiyomizu K, Usami S, Abe S, Shinkawa H, Komune S.
    Am J Otol; 1998 Nov 12; 19(6):754-7. PubMed ID: 9831149
    [Abstract] [Full Text] [Related]

  • 15. Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.
    Usami S, Abe S, Shinkawa H, Kimberling WJ.
    J Commun Disord; 1998 Nov 12; 31(5):423-34; quiz 434-5. PubMed ID: 9777488
    [Abstract] [Full Text] [Related]

  • 16. Audiovestibular findings in patients with mitochondrial A1555G mutation.
    Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K.
    Laryngoscope; 2004 Feb 12; 114(2):344-8. PubMed ID: 14755216
    [Abstract] [Full Text] [Related]

  • 17. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
    Ulubil SA, Furze AD, Angeli SI.
    J Laryngol Otol; 2006 Mar 12; 120(3):230-2. PubMed ID: 16359140
    [Abstract] [Full Text] [Related]

  • 18. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2005 Oct 28; 336(3):967-73. PubMed ID: 16168391
    [Abstract] [Full Text] [Related]

  • 19. Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA.
    Tamagawa Y, Kitamura K, Hagiwara H, Ishida T, Nishizawa M, Saito T, Iwamoto Y.
    Ann Otol Rhinol Laryngol; 1997 Apr 28; 106(4):338-42. PubMed ID: 9109727
    [Abstract] [Full Text] [Related]

  • 20. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
    Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct 28; 26(5):550-4. PubMed ID: 19806580
    [Abstract] [Full Text] [Related]

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