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99 related items for PubMed ID: 24252789

  • 1. 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; 164(2):413-5. PubMed ID: 24252789
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 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 11; 29(22):1936-40. PubMed ID: 26911053
    [Abstract] [Full Text] [Related]

  • 4. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
    [Abstract] [Full Text] [Related]

  • 5. 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 02; 115(4):640-4. PubMed ID: 15805873
    [Abstract] [Full Text] [Related]

  • 6. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
    Kupka S, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M.
    Hum Mutat; 2002 Mar 02; 19(3):308-9. PubMed ID: 11857751
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment.
    Ballana E, Morales E, Rabionet R, Montserrat B, Ventayol M, Bravo O, Gasparini P, Estivill X.
    Biochem Biophys Res Commun; 2006 Mar 24; 341(4):950-7. PubMed ID: 16458854
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Genetic susceptibility to aminoglycoside ototoxicity.
    Nguyen T, Jeyakumar A.
    Int J Pediatr Otorhinolaryngol; 2019 May 03; 120():15-19. PubMed ID: 30743189
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH, Reddy PP.
    Int J Audiol; 2008 Nov 03; 47(11):702-7. PubMed ID: 19031229
    [Abstract] [Full Text] [Related]

  • 12. Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family.
    Malik S, Sudoyo H, Sasmono T, Winata S, Arhya IN, Pramoonjago P, Sudana W, Marzuki S.
    J Hum Genet; 2003 Nov 03; 48(3):119-24. PubMed ID: 12624722
    [Abstract] [Full Text] [Related]

  • 13. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
    Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S.
    Auris Nasus Larynx; 2005 Jun 03; 32(2):119-24. PubMed ID: 15917167
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. [Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia].
    Dzhemileva LU, Posukh OL, Tazetdinov AM, Barashkov NA, Zhuravskiĭ SG, Ponidelko SN, Markova TG, Tadinova VN, Fedorova SA, Maksimova NR, Khusnutdinova EK.
    Genetika; 2009 Jul 10; 45(7):982-91. PubMed ID: 19705751
    [Abstract] [Full Text] [Related]

  • 16. 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 10; 32(4):785-94. PubMed ID: 23969527
    [Abstract] [Full Text] [Related]

  • 17. 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 10; 121(6):1184-6. PubMed ID: 21495045
    [Abstract] [Full Text] [Related]

  • 18. [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 Jun 10; 62(2):83-6. PubMed ID: 21129708
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment.
    de Moraes VC, Alexandrino F, Andrade PB, Câmara MF, Sartorato EL.
    Biochem Biophys Res Commun; 2009 Apr 03; 381(2):210-3. PubMed ID: 19338775
    [Abstract] [Full Text] [Related]

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