These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

154 related items for PubMed ID: 12882732

  • 1. [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]

  • 2. [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 12; 55(5):212-7. PubMed ID: 15461317
    [Abstract] [Full Text] [Related]

  • 3. Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
    Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX.
    Am J Med Genet A; 2005 Oct 01; 138A(2):133-40. PubMed ID: 16152638
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.
    Chen T, Liu Q, Jiang L, Liu C, Ou Q.
    Genet Test Mol Biomarkers; 2013 Feb 01; 17(2):122-30. PubMed ID: 23256547
    [Abstract] [Full Text] [Related]

  • 5. 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 01; 62(1):27-35. PubMed ID: 9490575
    [Abstract] [Full Text] [Related]

  • 6. [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 01; 30(6):728-34. PubMed ID: 18550495
    [Abstract] [Full Text] [Related]

  • 7. Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications.
    Casano RA, Johnson DF, Bykhovskaya Y, Torricelli F, Bigozzi M, Fischel-Ghodsian N.
    Am J Otolaryngol; 1999 Jun 01; 20(3):151-6. PubMed ID: 10326749
    [Abstract] [Full Text] [Related]

  • 8. [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]

  • 9. 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]

  • 10. [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 28; 53(9):641-8. PubMed ID: 12584878
    [Abstract] [Full Text] [Related]

  • 11. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH, Reddy PP.
    Int J Audiol; 2008 Nov 28; 47(11):702-7. PubMed ID: 19031229
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. [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 10; 26(5):550-4. PubMed ID: 19806580
    [Abstract] [Full Text] [Related]

  • 14. 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 10; 114(6):1085-91. PubMed ID: 15179218
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Pharmacogenomic testing to prevent aminoglycoside-induced hearing loss in cystic fibrosis patients: potential impact on clinical, patient, and economic outcomes.
    Veenstra DL, Harris J, Gibson RL, Rosenfeld M, Burke W, Watts C.
    Genet Med; 2007 Oct 10; 9(10):695-704. PubMed ID: 18073583
    [Abstract] [Full Text] [Related]

  • 18. 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 10; 122(10):1037-41. PubMed ID: 18282333
    [Abstract] [Full Text] [Related]

  • 19. Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.
    Scrimshaw BJ, Faed JM, Tate WP, Yun K.
    J Hum Genet; 1999 Oct 10; 44(6):388-90. PubMed ID: 10570910
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.