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Journal Abstract Search

208 related items for PubMed ID: 30523288

  • 1. 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; 64(3):199-206. PubMed ID: 30523288
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  • 2. The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.
    Ealy M, Lynch KA, Meyer NC, Smith RJ.
    Laryngoscope; 2011 Jun; 121(6):1184-6. PubMed ID: 21495045
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  • 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
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  • 6. 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; 111(2):366-372. PubMed ID: 34032273
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  • 10. Novel mutations affecting the secondary structure of MT-RNR1 gene: a causal relationship with profound nonsyndromic hearing impairment.
    Padma G, Ramchander PV, Nandur VU, Kumar KR, Padma T.
    Genet Test Mol Biomarkers; 2012 Sep; 16(9):1092-7. PubMed ID: 22852811
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  • 11. Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.
    Guaran V, Astolfi L, Castiglione A, Simoni E, Olivetto E, Galasso M, Trevisi P, Busi M, Volinia S, Martini A.
    Int J Mol Med; 2013 Oct; 32(4):785-94. PubMed ID: 23969527
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  • 12. Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss.
    Uehara DT, Rincon D, Abreu-Silva RS, Auricchio MT, Tabith A, Kok F, Mingroni-Netto RC.
    Genet Test Mol Biomarkers; 2010 Oct; 14(5):611-6. PubMed ID: 20722495
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  • 14. 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
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  • 16. 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; 52(2):98-103. PubMed ID: 23237192
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  • 20. Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides.
    Human H, Hagen CM, de Jong G, Harris T, Lombard D, Christiansen M, Bardien S.
    Biochem Biophys Res Commun; 2010 Mar 19; 393(4):751-6. PubMed ID: 20171168
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