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Journal Abstract Search

276 related items for PubMed ID: 12768662

  • 1. [Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss].
    Xing G, Bu X, Yan M, Lu L, Yang S.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 35(2):98-101. PubMed ID: 12768662
    [Abstract] [Full Text] [Related]

  • 2. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies.
    Zwirner P, Wilichowski E.
    Laryngoscope; 2001 Mar; 111(3):515-21. PubMed ID: 11224785
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  • 3. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
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  • 7. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S.
    Laryngoscope; 2004 Jun; 114(6):1085-91. PubMed ID: 15179218
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  • 9. Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation.
    Ishikawa K, Tamagawa Y, Takahashi K, Kimura H, Kusakari J, Hara A, Ichimura K.
    Laryngoscope; 2002 Aug; 112(8 Pt 1):1494-9. PubMed ID: 12172268
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  • 11. 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
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  • 12. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ, Mudde AH, 't Hart LM, Huygen PL, Cremers CW.
    Otol Neurotol; 2006 Sep 03; 27(6):802-8. PubMed ID: 16788417
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  • 13. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.
    Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H, Guan MX.
    J Med Genet; 2011 Oct 03; 48(10):682-90. PubMed ID: 21931169
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  • 14. 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 03; 74(9):1071-4. PubMed ID: 20637512
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  • 15. Prevalence of auditory neuropathy/synaptopathy in a population of children with profound hearing loss.
    Foerst A, Beutner D, Lang-Roth R, Huttenbrink KB, von Wedel H, Walger M.
    Int J Pediatr Otorhinolaryngol; 2006 Aug 03; 70(8):1415-22. PubMed ID: 16574250
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  • 16. Audiological findings of sensorineural deafness associated with a mutation in the mitochondrial DNA.
    Sawada S, Takeda T, Kakigi A, Saito H, Suehiro T, Nakauchi Y, Chikamori K.
    Am J Otol; 1997 May 03; 18(3):332-5. PubMed ID: 9149827
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  • 17. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec 03; (559):13-8. PubMed ID: 18340555
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  • 18. 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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  • 19. 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 Feb 10; 48(3):119-24. PubMed ID: 12624722
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  • 20. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.
    Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Sep 15; 348(1):200-5. PubMed ID: 16875663
    [Abstract] [Full Text] [Related]

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