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Journal Abstract Search

328 related items for PubMed ID: 30743189

  • 1. Genetic susceptibility to aminoglycoside ototoxicity.
    Nguyen T, Jeyakumar A.
    Int J Pediatr Otorhinolaryngol; 2019 May; 120():15-19. PubMed ID: 30743189
    [Abstract] [Full Text] [Related]

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

  • 3. [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; 29(22):1936-40. PubMed ID: 26911053
    [Abstract] [Full Text] [Related]

  • 4. Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides.
    Gürtler N, Schmuziger N, Kim Y, Mhatre AN, Jungi M, Lalwani AK.
    Laryngoscope; 2005 Apr; 115(4):640-4. PubMed ID: 15805873
    [Abstract] [Full Text] [Related]

  • 5. C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics.
    Postal M, Palodeto B, Sartorato EL, Oliveira CA.
    Braz J Otorhinolaryngol; 2009 Apr; 75(6):884-7. PubMed ID: 20209292
    [Abstract] [Full Text] [Related]

  • 6. 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; 117(1):9-15. PubMed ID: 15841390
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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 Apr 11; 20(3):151-6. PubMed ID: 10326749
    [Abstract] [Full Text] [Related]

  • 9. The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.
    Igumnova V, Veidemane L, Vīksna A, Capligina V, Zole E, Ranka R.
    J Hum Genet; 2019 Mar 11; 64(3):199-206. PubMed ID: 30523288
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy.
    Elstner M, Schmidt C, Zingler VC, Prokisch H, Bettecken T, Elson JL, Rudolph G, Bender A, Halmagyi GM, Brandt T, Strupp M, Klopstock T.
    Biochem Biophys Res Commun; 2008 Dec 12; 377(2):379-383. PubMed ID: 18851951
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.
    Guan MX.
    Mitochondrion; 2011 Mar 12; 11(2):237-45. PubMed ID: 21047563
    [Abstract] [Full Text] [Related]

  • 12. Mitochondrial mutations associated with aminoglycoside ototoxicity and hearing loss susceptibility identified by meta-analysis.
    Jing W, Zongjie H, Denggang F, Na H, Bin Z, Aifen Z, Xijiang H, Cong Y, Yunping D, Ring HZ, Ring BZ.
    J Med Genet; 2015 Feb 12; 52(2):95-103. PubMed ID: 25515069
    [Abstract] [Full Text] [Related]

  • 13. Genetic factors in aminoglycoside toxicity.
    Fischel-Ghodsian N.
    Ann N Y Acad Sci; 1999 Nov 28; 884():99-109. PubMed ID: 10842587
    [Abstract] [Full Text] [Related]

  • 14. Aminoglycoside-induced ototoxicity.
    Selimoglu E.
    Curr Pharm Des; 2007 Nov 28; 13(1):119-26. PubMed ID: 17266591
    [Abstract] [Full Text] [Related]

  • 15. Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
    Shen Z, Zheng J, Chen B, Peng G, Zhang T, Gong S, Zhu Y, Zhang C, Li R, Yang L, Zhou J, Cai T, Jin L, Lu J, Guan MX.
    J Transl Med; 2011 Jan 04; 9():4. PubMed ID: 21205314
    [Abstract] [Full Text] [Related]

  • 16. 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 04; 164(2):413-5. PubMed ID: 24252789
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype.
    McDermott JH, Wolf J, Hoshitsuki K, Huddart R, Caudle KE, Whirl-Carrillo M, Steyger PS, Smith RJH, Cody N, Rodriguez-Antona C, Klein TE, Newman WG.
    Clin Pharmacol Ther; 2022 Feb 10; 111(2):366-372. PubMed ID: 34032273
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.
    Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S.
    Am J Otolaryngol; 1993 Feb 10; 14(6):399-403. PubMed ID: 8285309
    [Abstract] [Full Text] [Related]

  • 20. Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.
    Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X.
    Biochem Biophys Res Commun; 2006 Aug 11; 346(4):1131-5. PubMed ID: 16782057
    [Abstract] [Full Text] [Related]

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