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Journal Abstract Search

264 related items for PubMed ID: 18279408

  • 1. Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.
    Katulanda P, Groves CJ, Barrett A, Sheriff R, Matthews DR, McCarthy MI, Gloyn AL.
    Diabet Med; 2008 Mar; 25(3):370-4. PubMed ID: 18279408
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  • 3. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
    Newkirk JE, Taylor RW, Howell N, Bindoff LA, Chinnery PF, Alberti KG, Turnbull DM, Walker M.
    Diabet Med; 1997 Jun; 14(6):457-60. PubMed ID: 9212310
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  • 4. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S, Hinokio Y, Ohtomo M, Hirai M, Hirai A, Chiba M, Kasuga S, Satoh Y, Akai H, Toyota T.
    Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
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  • 8. [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
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  • 10. Prevalence and projections of diabetes and pre-diabetes in adults in Sri Lanka--Sri Lanka Diabetes, Cardiovascular Study (SLDCS).
    Katulanda P, Constantine GR, Mahesh JG, Sheriff R, Seneviratne RD, Wijeratne S, Wijesuriya M, McCarthy MI, Adler AI, Matthews DR.
    Diabet Med; 2008 Sep; 25(9):1062-9. PubMed ID: 19183311
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  • 20. Search for mitochondrial DNA mutation at position 3243 in German patients with a positive family history of maternal diabetes mellitus.
    Klemm T, Neumann S, Trülzsch B, Pistrosch F, Hanefeld M, Paschke R.
    Exp Clin Endocrinol Diabetes; 2001 Sep; 109(5):283-7. PubMed ID: 11507652
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