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131 related items for PubMed ID: 8544627

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
    [Abstract] [Full Text] [Related]

  • 4. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
    [Abstract] [Full Text] [Related]

  • 5. Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA.
    Tamagawa Y, Kitamura K, Hagiwara H, Ishida T, Nishizawa M, Saito T, Iwamoto Y.
    Ann Otol Rhinol Laryngol; 1997 Apr; 106(4):338-42. PubMed ID: 9109727
    [Abstract] [Full Text] [Related]

  • 6. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.
    Katagiri H, Asano T, Ishihara H, Inukai K, Anai M, Yamanouchi T, Tsukuda K, Kikuchi M, Kitaoka H, Ohsawa N.
    Diabetologia; 1994 May; 37(5):504-10. PubMed ID: 8056189
    [Abstract] [Full Text] [Related]

  • 7. [Audiologic evaluation in a family showing diabetes mellitus and deafness associated with a mutation in mitochondrial DNA].
    Tamagawa Y, Tanaka H, Hagiwara H, Ishida T, Kitamura K.
    Nihon Jibiinkoka Gakkai Kaiho; 1995 Aug; 98(8):1257-62. PubMed ID: 7472762
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome.
    Choo-Kang AT, Lynn S, Taylor GA, Daly ME, Sihota SS, Wardell TM, Chinnery PF, Turnbull DM, Walker M.
    Diabetes; 2002 Jul; 51(7):2317-20. PubMed ID: 12086967
    [Abstract] [Full Text] [Related]

  • 10. Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome.
    Oshima T, Ueda N, Ikeda K, Abe K, Takasaka T.
    Laryngoscope; 1996 Jan; 106(1 Pt 1):43-8. PubMed ID: 8544626
    [Abstract] [Full Text] [Related]

  • 11. Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus.
    Shigemoto M, Yoshimasa Y, Yamamoto Y, Hayashi T, Suga J, Inoue G, Okamoto M, Jingami H, Tsuda K, Yamamoto T, Yagura T, Oishi M, Tsujii S, Kuzuya H, Nakao K.
    Intern Med; 1998 Mar; 37(3):265-72. PubMed ID: 9617861
    [Abstract] [Full Text] [Related]

  • 12. Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome.
    Howes T, Madden C, Dasgupta S, Saeed S, Das V.
    J Laryngol Otol; 2008 Nov; 122(11):1249-52. PubMed ID: 18950542
    [Abstract] [Full Text] [Related]

  • 13. [Prevalence and clinical characteristics of the mitochondrial tRNA(Leu(UUR)) gene 3243 A to G mutation in familial diabetes mellitus in Chinese population].
    Wang SJ, Wu SH, Zheng TS, Wang L, Lu HJ, Xiang KS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):191-5. PubMed ID: 19350514
    [Abstract] [Full Text] [Related]

  • 14. A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNA(Leu (UUR))) applied to a Norwegian family with diabetes mellitus and hearing loss.
    Akbari M, Skjelbred C, Følling I, Sagen J, Krokan HE.
    Scand J Clin Lab Invest; 2004 Apr; 64(2):86-92. PubMed ID: 15115244
    [Abstract] [Full Text] [Related]

  • 15. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
    Xiu L, Zhang Q, Yu B.
    Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.
    Jansen JJ, Maassen JA, van der Woude FJ, Lemmink HA, van den Ouweland JM, t' Hart LM, Smeets HJ, Bruijn JA, Lemkes HH.
    J Am Soc Nephrol; 1997 Jul; 8(7):1118-24. PubMed ID: 9219161
    [Abstract] [Full Text] [Related]

  • 18. Diminished insulin secretory response to glucose but normal insulin and glucagon secretory responses to arginine in a family with maternally inherited diabetes and deafness caused by mitochondrial tRNA(LEU(UUR)) gene mutation.
    Brändle M, Lehmann R, Maly FE, Schmid C, Spinas GA.
    Diabetes Care; 2001 Jul; 24(7):1253-8. PubMed ID: 11423511
    [Abstract] [Full Text] [Related]

  • 19. Renal complications in a patient with A-to-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.
    Hirano M, Konishi K, Arata N, Iyori M, Saruta T, Kuramochi S, Akizuki M.
    Intern Med; 2002 Feb; 41(2):113-8. PubMed ID: 11868597
    [Abstract] [Full Text] [Related]

  • 20. [Detection of a mutation in mitochondrial DNA in a family with sensorineural deafness and diabetes mellitus as the predominant clinical features].
    Tamagawa Y, Tanaka H, Hagiwara H, Ishida T, Kitamura K, Nishizawa M.
    Nihon Jibiinkoka Gakkai Kaiho; 1995 Jul; 98(7):1104-10. PubMed ID: 7562231
    [Abstract] [Full Text] [Related]

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