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147 related items for PubMed ID: 9777488

  • 1. 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; 31(5):423-34; quiz 434-5. PubMed ID: 9777488
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
    Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Papadopoulou E, Neou P, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB.
    Biochem Biophys Res Commun; 2009 Dec 18; 390(3):755-7. PubMed ID: 19835846
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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 25; 62(4):303-5. PubMed ID: 12372057
    [Abstract] [Full Text] [Related]

  • 6. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
    Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ.
    Eur J Hum Genet; 1998 Oct 25; 6(6):563-9. PubMed ID: 9887373
    [Abstract] [Full Text] [Related]

  • 7. [Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment].
    Morales Angulo C, Gallo-Terán J, Señaris B, Fontalva A, González-Aguado R, Fernández-Luna JL.
    Acta Otorrinolaringol Esp; 2011 Oct 25; 62(2):83-6. PubMed ID: 21129708
    [Abstract] [Full Text] [Related]

  • 8. [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 25; 35(2):98-101. PubMed ID: 12768662
    [Abstract] [Full Text] [Related]

  • 9. A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition.
    Bai YH, Ren CC, Gong XR, Meng LP.
    J Laryngol Otol; 2008 Oct 25; 122(10):1037-41. PubMed ID: 18282333
    [Abstract] [Full Text] [Related]

  • 10. Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation.
    Hutchin TP, Lench NJ, Arbuzova S, Markham AF, Mueller RF.
    Eur J Hum Genet; 2001 Jan 25; 9(1):56-8. PubMed ID: 11175301
    [Abstract] [Full Text] [Related]

  • 11. [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 25; 22(2):125-8. PubMed ID: 15793769
    [Abstract] [Full Text] [Related]

  • 12. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.
    Li Z, Li R, Chen J, Liao Z, Zhu Y, Qian Y, Xiong S, Heman-Ackah S, Wu J, Choo DI, Guan MX.
    Hum Genet; 2005 Jun 25; 117(1):9-15. PubMed ID: 15841390
    [Abstract] [Full Text] [Related]

  • 13. [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 25; 53(9):641-8. PubMed ID: 12584878
    [Abstract] [Full Text] [Related]

  • 14. 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 25; 114(2):153-60. PubMed ID: 15757197
    [Abstract] [Full Text] [Related]

  • 15. Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.
    Malik SG, Pieter N, Sudoyo H, Kadir A, Marzuki S.
    J Hum Genet; 2003 Feb 25; 48(9):480-483. PubMed ID: 12955586
    [Abstract] [Full Text] [Related]

  • 16. Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.
    Nahili H, Charif M, Boulouiz R, Bounaceur S, Benrahma H, Abidi O, Chafik A, Rouba H, Kandil M, Barakat A.
    Int J Pediatr Otorhinolaryngol; 2010 Sep 25; 74(9):1071-4. PubMed ID: 20637512
    [Abstract] [Full Text] [Related]

  • 17. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S, Forli F, Passetti S, Rocchi A, Pollina L, Cecchetti D, Mancuso M, Siciliano G.
    Biosci Rep; 2008 Feb 25; 28(1):49-59. PubMed ID: 18215147
    [Abstract] [Full Text] [Related]

  • 18. Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.
    Maniglia LP, Moreira BCL, da Silva MAOM, Piatto VB, Maniglia JV.
    Braz J Otorhinolaryngol; 2008 Feb 25; 74(5):731-736. PubMed ID: 19082356
    [Abstract] [Full Text] [Related]

  • 19. A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome.
    Park MK, Sagong B, Lee JD, Bae SH, Lee B, Choi KS, Choo YS, Lee KY, Kim UK.
    Int J Pediatr Otorhinolaryngol; 2014 Nov 25; 78(11):1996-9. PubMed ID: 25223473
    [Abstract] [Full Text] [Related]

  • 20. 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 25; 120(3):230-2. PubMed ID: 16359140
    [Abstract] [Full Text] [Related]

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