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Journal Abstract Search

108 related items for PubMed ID: 8973709

  • 1. Mitochondrial DNA mutation at nucleotide 1555 in a patient with bilateral sensorineural hearing loss of unknown etiology.
    Tamagawa Y, Kitamura K, Ishida T, Hagiwara H, Abe K, Nishizawa M.
    Acta Otolaryngol; 1996 Nov; 116(6):796-8. PubMed ID: 8973709
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  • 2. Hearing loss with a mitochondrial gene mutation is highly prevalent in Japan.
    Oshima T, Ueda N, Ikeda K, Abe K, Takasaka T.
    Laryngoscope; 1999 Feb; 109(2 Pt 1):334-8. PubMed ID: 10890789
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  • 5. Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.
    Rodríguez-Ballesteros M, Olarte M, Aguirre LA, Galán F, Galán R, Vallejo LA, Navas C, Villamar M, Moreno-Pelayo MA, Moreno F, del Castillo I.
    J Med Genet; 2006 Nov; 43(11):e54. PubMed ID: 17085680
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  • 10. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene.
    Yamasoba T, Oka Y, Tsukuda K, Nakamura M, Kaga K.
    Laryngoscope; 1996 Jan; 106(1 Pt 1):49-53. PubMed ID: 8544627
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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; 27(6):802-8. PubMed ID: 16788417
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  • 14. [Modification factors associated with maternally inherited non-syndromic hearing loss].
    Hong WJ, Zheng BJ, Qian JF, Wu H, Jin H, Zhu YT.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Jun 07; 52(6):472-477. PubMed ID: 28635225
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  • 18. A review of cochlear implantation in mitochondrial sensorineural hearing loss.
    Sinnathuray AR, Raut V, Awa A, Magee A, Toner JG.
    Otol Neurotol; 2003 May 07; 24(3):418-26. PubMed ID: 12806294
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