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Journal Abstract Search

339 related items for PubMed ID: 16359140

  • 21. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
    Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ.
    Eur J Hum Genet; 1998; 6(6):563-9. PubMed ID: 9887373
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  • 22. Evaluation of auditory perception skills development in profoundly deaf children following cochlear implantation.
    Zakirullah, Mukhtar N, Khan MI, Ahsan M, Shah SA.
    J Ayub Med Coll Abbottabad; 2008; 20(1):94-7. PubMed ID: 19024198
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  • 23. Cochlear implants in elderly people: preliminary results.
    Sterkers O, Mosnier I, Ambert-Dahan E, Herelle-Dupuy E, Bozorg-Grayeli A, Bouccara D.
    Acta Otolaryngol Suppl; 2004 May; (552):64-7. PubMed ID: 15219050
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  • 27. 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
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  • 29. Effect of preoperative residual hearing on speech perception after cochlear implantation.
    Adunka OF, Buss E, Clark MS, Pillsbury HC, Buchman CA.
    Laryngoscope; 2008 Nov 28; 118(11):2044-9. PubMed ID: 18813141
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  • 30. 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
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  • 31. 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 10; 74(9):1071-4. PubMed ID: 20637512
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  • 32. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.
    Jin L, Yang A, Zhu Y, Zhao J, Wang X, Yang L, Sun D, Tao Z, Tsushima A, Wu G, Xu L, Chen C, Yi B, Cai J, Tang X, Wang J, Li D, Yuan Q, Liao Z, Chen J, Li Z, Lu J, Guan MX.
    Biochem Biophys Res Commun; 2007 Sep 14; 361(1):133-9. PubMed ID: 17659260
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  • 33. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
    Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct 14; 26(5):550-4. PubMed ID: 19806580
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  • 35. Auditory performance of cochlear implant children aged 2-5 years.
    Thawin C, Kanchanalarp C, Lertsukprasert K, Cheewaruangroj W, Khantapasuantara K, Ruencharoen S.
    J Med Assoc Thai; 2006 Nov 14; 89(11):1923-7. PubMed ID: 17205875
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  • 36. Cochlear implantation in complete remission in a patient with leukemia.
    Takeuchi K, Hattori T, Masuda S, Usui S, Oka K, Sakaida H, Majima Y.
    Acta Otolaryngol; 2008 Jul 14; 128(7):821-3. PubMed ID: 18568527
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  • 39. 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 Jul 14; 48(3):119-24. PubMed ID: 12624722
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