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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

339 related items for PubMed ID: 16359140

  • 61. Hearing evaluation in two sisters with a T8993G point mutation of mitochondrial DNA.
    Sakai Y, Kaga K, Kodama K, Higuchi A, Miyamoto J.
    Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):1115-9. PubMed ID: 15236904
    [Abstract] [Full Text] [Related]

  • 62. [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; 53(9):641-8. PubMed ID: 12584878
    [Abstract] [Full Text] [Related]

  • 63. Unilateral Cochlear Implants for Severe, Profound, or Moderate Sloping to Profound Bilateral Sensorineural Hearing Loss: A Systematic Review and Consensus Statements.
    Buchman CA, Gifford RH, Haynes DS, Lenarz T, O'Donoghue G, Adunka O, Biever A, Briggs RJ, Carlson ML, Dai P, Driscoll CL, Francis HW, Gantz BJ, Gurgel RK, Hansen MR, Holcomb M, Karltorp E, Kirtane M, Larky J, Mylanus EAM, Roland JT, Saeed SR, Skarzynski H, Skarzynski PH, Syms M, Teagle H, Van de Heyning PH, Vincent C, Wu H, Yamasoba T, Zwolan T.
    JAMA Otolaryngol Head Neck Surg; 2020 Oct 01; 146(10):942-953. PubMed ID: 32857157
    [Abstract] [Full Text] [Related]

  • 64. Bilateral cochlear implantation in a patient with long-term deafness.
    Portmann D, Felix F, Negrevergne M, Bourdin M, Lagourgue P, Coulomb-Faye F, Polanski FJ.
    Rev Laryngol Otol Rhinol (Bord); 2007 Oct 01; 128(1-2):65-8. PubMed ID: 17633669
    [Abstract] [Full Text] [Related]

  • 65. Simultaneous translabyrinthine removal of acoustic neuroma and cochlear implantation.
    Zanetti D, Campovecchi CB, Pasini S, Nassif N.
    Auris Nasus Larynx; 2008 Dec 01; 35(4):562-8. PubMed ID: 18243617
    [Abstract] [Full Text] [Related]

  • 66. [Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
    Liu X, Dai P, Huang DL, Yuan HJ, Li WM, Cao JY, Yu F, Zhang RN, Lin HY, Zhu XH, He Y, Yu YJ, Yao K.
    Zhonghua Yi Xue Za Zhi; 2006 May 23; 86(19):1318-22. PubMed ID: 16796900
    [Abstract] [Full Text] [Related]

  • 67. Cochlear implantation in a patient with deafness induced by Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathies).
    Postelmans JT, Stokroos RJ.
    J Laryngol Otol; 2006 Jun 23; 120(6):508-10. PubMed ID: 16772060
    [Abstract] [Full Text] [Related]

  • 68. Mitochondrial 12S ribosomal RNA A1555G mutation associated with cardiomyopathy and hearing loss following high-dose chemotherapy and repeated aminoglycoside exposure.
    Skou AS, Tranebjærg L, Jensen T, Hasle H.
    J Pediatr; 2014 Feb 23; 164(2):413-5. PubMed ID: 24252789
    [Abstract] [Full Text] [Related]

  • 69. A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.
    Chaig MR, Zernotti ME, Soria NW, Romero OF, Romero MF, Gerez NM.
    Biochem Biophys Res Commun; 2008 Apr 11; 368(3):631-6. PubMed ID: 18261986
    [Abstract] [Full Text] [Related]

  • 70. Rapid mass screening method and counseling for the 1555A-->G mitochondrial mutation.
    Usami S, Abe S, Shinkawa H, Inoue Y, Yamaguchi T.
    J Hum Genet; 1999 Apr 11; 44(5):304-7. PubMed ID: 10496072
    [Abstract] [Full Text] [Related]

  • 71. [Nonsyndromic inherited hearing impairment caused by mtDNA double mutations of A1555G and 961 insC].
    Cao X, Xing GQ, Wei QJ, Bu XK, Wang DY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec 11; 21(6):629-32. PubMed ID: 15583999
    [Abstract] [Full Text] [Related]

  • 72. Combined microtia and aural atresia: issues in cochlear implantation.
    Lin K, Marrinan MS, Shapiro WH, Kenna MA, Cohen NL.
    Laryngoscope; 2005 Jan 11; 115(1):39-43. PubMed ID: 15630363
    [Abstract] [Full Text] [Related]

  • 73. The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing loss.
    Scrimshaw BJ, Faed JM, Tate WP, Yun K.
    N Z Med J; 1999 Jun 11; 112(1089):216-7. PubMed ID: 10414625
    [No Abstract] [Full Text] [Related]

  • 74. Novel mutation in the homeobox domain of transcription factor POU3F4 associated with profound sensorineural hearing loss.
    Schild C, Prera E, Lüblinghoff N, Arndt S, Aschendorff A, Birkenhäger R.
    Otol Neurotol; 2011 Jun 11; 32(4):690-4. PubMed ID: 21555964
    [Abstract] [Full Text] [Related]

  • 75. The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.
    ØStergaard E, Montserrat-Sentis B, Grønskov K, Brøndum-Nielsen K.
    Clin Genet; 2002 Oct 11; 62(4):303-5. PubMed ID: 12372057
    [Abstract] [Full Text] [Related]

  • 76. [Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity].
    Gallo-Terán J, Arellano B, Morales-Angulo C, Modamio-Høybjør S, Moreno-Pelayo MA, Ramírez-Camacho R, del Castillo I, Moreno F.
    Acta Otorrinolaringol Esp; 2004 May 11; 55(5):212-7. PubMed ID: 15461317
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  • 78. Residual hearing thresholds in cochlear implantation and reimplantation.
    Di Nardo W, Cantore I, Cianfrone F, Melillo P, Rigante M, Paludetti G.
    Audiol Neurootol; 2007 May 11; 12(3):165-9. PubMed ID: 17259703
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