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187 related items for PubMed ID: 18568513

  • 1. Audiological and genetic features of the mtDNA mutations.
    Liu XZ, Angeli S, Ouyang XM, Liu W, Ke XM, Liu YH, Liu SX, Du LL, Deng XW, Yuan H, Yan D.
    Acta Otolaryngol; 2008 Jul; 128(7):732-8. PubMed ID: 18568513
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
    Tang X, Yang L, Zhu Y, Liao Z, Wang J, Qian Y, Tao Z, Hu L, Wu G, Lan J, Wang X, Ji J, Wu J, Ji Y, Feng J, Chen J, Li Z, Zhang X, Lu J, Guan MX.
    Gene; 2007 May 15; 393(1-2):11-9. PubMed ID: 17341440
    [Abstract] [Full Text] [Related]

  • 4. [Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].
    Yang AF, Zhu Y, Lu JX, Yang L, Zhao JY, Sun DM.
    Yi Chuan; 2008 Jun 15; 30(6):728-34. PubMed ID: 18550495
    [Abstract] [Full Text] [Related]

  • 5. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.
    Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Benedict-Alderfer C, Zheng QY, Wang QJ.
    Acta Otolaryngol; 2011 Feb 15; 131(2):124-9. PubMed ID: 21162657
    [Abstract] [Full Text] [Related]

  • 6. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.
    Estivill X, Govea N, Barceló E, Badenas C, Romero E, Moral L, Scozzri R, D'Urbano L, Zeviani M, Torroni A.
    Am J Hum Genet; 1998 Jan 15; 62(1):27-35. PubMed ID: 9490575
    [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 Jan 15; 62(2):83-6. PubMed ID: 21129708
    [Abstract] [Full Text] [Related]

  • 8. 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 Jan 15; 74(5):731-736. PubMed ID: 19082356
    [Abstract] [Full Text] [Related]

  • 9. Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.
    Wei Q, Xu D, Chen Z, Li H, Lu Y, Liu C, Bu X, Xing G, Cao X.
    Int J Audiol; 2013 Feb 15; 52(2):98-103. PubMed ID: 23237192
    [Abstract] [Full Text] [Related]

  • 10. Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.
    Moassass F, Al-Halabi B, Nweder MS, Al-Achkar W.
    Int J Pediatr Otorhinolaryngol; 2018 Oct 15; 113():110-114. PubMed ID: 30173967
    [Abstract] [Full Text] [Related]

  • 11. [Mitochondrial DNA A1555G mutation analysis in 802 nonsyndromic hearing impairment patients].
    Liu XW, Guo YF, Han DY, Zhao YL, Lan L, Zhao C, Wang QJ.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Oct 15; 42(10):739-42. PubMed ID: 18229583
    [Abstract] [Full Text] [Related]

  • 12. [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 15; 53(9):641-8. PubMed ID: 12584878
    [Abstract] [Full Text] [Related]

  • 13. Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.
    Montazer Zohour M, Tabatabaiefar MA, Dehkordi FA, Farrokhi E, Akbari MT, Chaleshtori MH.
    Genet Test Mol Biomarkers; 2012 Apr 15; 16(4):271-8. PubMed ID: 22077646
    [Abstract] [Full Text] [Related]

  • 14. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
    Qu J, Wang J, Xu S.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov 15; 29(22):1936-40. PubMed ID: 26911053
    [Abstract] [Full Text] [Related]

  • 15. [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 15; 26(5):550-4. PubMed ID: 19806580
    [Abstract] [Full Text] [Related]

  • 16. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
    [Abstract] [Full Text] [Related]

  • 17. [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 03; 35(2):98-101. PubMed ID: 12768662
    [Abstract] [Full Text] [Related]

  • 18. 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 03; 114(6):1085-91. PubMed ID: 15179218
    [Abstract] [Full Text] [Related]

  • 19. 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 03; 120(3):230-2. PubMed ID: 16359140
    [Abstract] [Full Text] [Related]

  • 20. 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 Mar 03; 48(9):480-483. PubMed ID: 12955586
    [Abstract] [Full Text] [Related]

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