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Journal Abstract Search

131 related items for PubMed ID: 12584878

  • 41. The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients.
    Rydzanicz M, Cywińska K, Wróbel M, Pollak A, Gawęcki W, Wojsyk-Banaszak I, Lechowicz U, Mueller-Malesińska M, Ołdak M, Płoski R, Skarżyński H, Szyfter K, Szyfter W.
    Mol Genet Metab; 2011; 104(1-2):153-9. PubMed ID: 21621438
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  • 42. Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.
    Usami S, Abe S, Kasai M, Shinkawa H, Moeller B, Kenyon JB, Kimberling WJ.
    Laryngoscope; 1997 Apr; 107(4):483-90. PubMed ID: 9111378
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  • 43. Vestibular evoked myogenic potentials in patients with the mitochondrial A1555G mutation.
    Kawashima Y, Noguchi Y, Ito T, Kitamura K.
    Laryngoscope; 2009 Sep; 119(9):1874-9. PubMed ID: 19536740
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  • 44. Hearing loss due to the mitochondrial A1555G mutation in Italian families.
    Casano RA, Bykhovskaya Y, Johnson DF, Hamon M, Torricelli F, Bigozzi M, Fischel-Ghodsian N.
    Am J Med Genet; 1998 Oct 12; 79(5):388-91. PubMed ID: 9779807
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  • 45. [Audiologic analysis of a family with nonsyndromic genetic progressive sensorineural hearing loss].
    Ni D, Dan H, Mo J.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1999 Apr 12; 34(2):77-80. PubMed ID: 12764852
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  • 46. Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation.
    Zhu Y, Huang S, Kang D, Han M, Wang G, Yuan Y, Su Y, Yuan H, Zhai S, Dai P.
    BMC Genet; 2014 Feb 17; 15():26. PubMed ID: 24533451
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  • 47. 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 17; 19(3):308-9. PubMed ID: 11857751
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  • 51. MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene.
    Ballana E, Mercader JM, Fischel-Ghodsian N, Estivill X.
    BMC Med Genet; 2007 Dec 21; 8():81. PubMed ID: 18154640
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  • 52. 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 Dec 21; 48(3):119-24. PubMed ID: 12624722
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  • 53. Audiometric characteristics of a Dutch family with Muckle-Wells syndrome.
    Weegerink NJ, Schraders M, Leijendeckers J, Slieker K, Huygen PL, Hoefsloot L, Oostrik J, Pennings RJ, Simon A, Snik A, Kremer H, Kunst HP.
    Hear Res; 2011 Dec 21; 282(1-2):243-51. PubMed ID: 21810457
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  • 56. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep 21; 113(9):1623-9. PubMed ID: 12972945
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  • 57. Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.
    Weegerink NJ, Huygen PL, Schraders M, Kremer H, Pennings RJ, Kunst HP.
    Hear Res; 2011 Dec 21; 282(1-2):167-77. PubMed ID: 21893181
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  • 58. Bilateral sensorineural hearing loss in members of a maternal lineage with mitochondrial point mutation.
    Vernham GA, Reid FM, Rundle PA, Jacobs HT.
    Clin Otolaryngol Allied Sci; 1994 Aug 21; 19(4):314-9. PubMed ID: 7994888
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  • 60. High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy.
    Matsushima K, Nakano A, Arimoto Y, Mutai H, Yamazawa K, Murayama K, Matsunaga T.
    Int J Pediatr Otorhinolaryngol; 2018 May 21; 108():125-131. PubMed ID: 29605341
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