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Journal Abstract Search

94 related items for PubMed ID: 10496072

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  • 23. [The relation between mitochondrial DNA mutation and aminogly- coside antibiotics-induced deafness].
    Zhang L, Lu M, Huang Y, Zhou X, Qiu D, Wang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):138-40. PubMed ID: 10359860
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  • 24. 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 Jun; 74(5):731-736. PubMed ID: 19082356
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  • 27. Aminoglycoside-induced deafness during treatment of acute leukaemia.
    Bitner-Glindzicz M, Osei-Lah V, Colvin I, Sirimanna T, Lucas D, Mac Ardle B, Webb D, Shankar A, Kingston J, Jenkins L, Rahman S.
    Arch Dis Child; 2010 Feb; 95(2):153-5. PubMed ID: 20172897
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  • 28. Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants.
    Göpel W, Berkowski S, Preuss M, Ziegler A, Küster H, Felderhoff-Müser U, Gortner L, Mögel M, Härtel C, Herting E, German Neonatal Network.
    BMC Pediatr; 2014 Aug 26; 14():210. PubMed ID: 25155176
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  • 30. Sequence analysis of the mitochondrial genome from a large family with maternally inherited nonsyndromic deafness.
    Zhang HJ, Xu CH, Zhan YJ, Zhao SY, Shan YF, Geng XX, Shan XN.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug 26; 22(4):368-71. PubMed ID: 16086269
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  • 32. Maternally inherited deafness associated with a T1095C mutation in the mDNA.
    Tessa A, Giannotti A, Tieri L, Vilarinho L, Marotta G, Santorelli FM.
    Eur J Hum Genet; 2001 Feb 26; 9(2):147-9. PubMed ID: 11313749
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  • 34. [Mitochondrial DNA 3243, 3316 point mutations and type 2 diabetes mellitus].
    Tang J, Li J, Tian X, Kong Q, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 26; 22(2):198-200. PubMed ID: 15793785
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  • 36. [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
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  • 37. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
    Chapiro E, Feldmann D, Denoyelle F, Sternberg D, Jardel C, Eliot MM, Bouccara D, Weil D, Garabédian EN, Couderc R, Petit C, Marlin S.
    Eur J Hum Genet; 2002 Dec 23; 10(12):851-6. PubMed ID: 12461693
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