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Journal Abstract Search

187 related items for PubMed ID: 18568513

  • 21. [Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].
    Zhang CQ, Chen BB, Chen YY, Liu XJ, Zheng J, Gao JJ, Huang SY, Nan BY, Zhang YY, Yu X, Guan MX.
    Yi Chuan; 2013 Mar; 35(3):352-8. PubMed ID: 23575541
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  • 23. Aminoglycoside-associated nonsyndromic deafness and speech disorder in mitochondrial A1555G mutation in a family: A case report.
    Ou YH, Chen AW, Fan JY, Cheng WL, Lin TT, Chen MK, Liu CS.
    Medicine (Baltimore); 2018 Oct; 97(42):e12878. PubMed ID: 30335006
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  • 24. Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.
    Vivero RJ, Ouyang X, Yan D, Du L, Liu W, Angeli SI, Liu XZ.
    Genet Test Mol Biomarkers; 2012 Sep; 16(9):1146-8. PubMed ID: 22853457
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  • 25. Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.
    Nahili H, Charif M, Boulouiz R, Bounaceur S, Benrahma H, Abidi O, Chafik A, Rouba H, Kandil M, Barakat A.
    Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1071-4. PubMed ID: 20637512
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  • 27. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S.
    Ann Otol Rhinol Laryngol; 2005 Feb; 114(2):153-60. PubMed ID: 15757197
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  • 28. 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
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  • 29. GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.
    Guo YF, Liu XW, Guan J, Han MK, Wang DY, Zhao YL, Rao SQ, Wang QJ.
    Acta Otolaryngol; 2008 Mar 01; 128(3):297-303. PubMed ID: 18274916
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  • 31. The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
    Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Papadopoulou E, Neou P, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB.
    Biochem Biophys Res Commun; 2009 Dec 18; 390(3):755-7. PubMed ID: 19835846
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  • 32. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC, Chiu YH, Chen PJ, Hsu CJ.
    Ear Hear; 2007 Jun 18; 28(3):332-42. PubMed ID: 17485982
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  • 34. Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.
    Zhu Y, Li Q, Chen Z, Kun Y, Liu L, Liu X, Yuan H, Zhai S, Han D, Dai P.
    Mitochondrion; 2009 Nov 18; 9(6):418-28. PubMed ID: 19682603
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  • 35. GJB2 and mitochondrial DNA 1555A>G mutations in students with hearing loss in the Hubei Province of China.
    Chen G, He F, Fu S, Dong J.
    Int J Pediatr Otorhinolaryngol; 2011 Sep 18; 75(9):1156-9. PubMed ID: 21777984
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  • 40. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S, Forli F, Passetti S, Rocchi A, Pollina L, Cecchetti D, Mancuso M, Siciliano G.
    Biosci Rep; 2008 Feb 18; 28(1):49-59. PubMed ID: 18215147
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