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Journal Abstract Search

345 related items for PubMed ID: 9628277

  • 1. 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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  • 6. Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.
    Maassen JA, van den Ouweland JM, t Hart LM, Lemkes HH.
    Horm Metab Res; 1997 Feb; 29(2):50-5. PubMed ID: 9105898
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  • 7. [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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  • 8. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].
    Maassen JA, Jansen JJ, van den Ouweland JM, Hart LM, van Essen EH, Lemkes HH.
    Ned Tijdschr Geneeskd; 1998 Jan 31; 142(5):229-33. PubMed ID: 9557035
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  • 9. 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 31; 25(3):370-4. PubMed ID: 18279408
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  • 11. Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.
    Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C.
    Biochem Biophys Res Commun; 2000 Nov 02; 277(3):771-5. PubMed ID: 11062027
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  • 14. 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 02; 14(6):457-60. PubMed ID: 9212310
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  • 16. 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 02; 24(7):1253-8. PubMed ID: 11423511
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