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Journal Abstract Search

1007 related items for PubMed ID: 10366077

  • 41. [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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  • 42. Pigmentary retinopathy in patients with the MELAS mutation 3243A-->G in mitochondrial DNA.
    Latvala T, Mustonen E, Uusitalo R, Majamaa K.
    Graefes Arch Clin Exp Ophthalmol; 2002 Oct; 240(10):795-801. PubMed ID: 12397426
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  • 45. The molecular basis and clinical characteristics of Maternally Inherited Diabetes and Deafness (MIDD), a recently recognized diabetic subtype.
    Maassen JA, Jansen JJ, Kadowaki T, van den Ouweland JM, 't Hart LM, Lemkes HH.
    Exp Clin Endocrinol Diabetes; 1996 Oct; 104(3):205-11. PubMed ID: 8817237
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  • 46. 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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  • 49. Mitochondrial tRNA(Leu(UUR)) gene mutation diabetes mellitus in Chinese.
    Xiang K, Wang Y, Wu S, Lu H, Zheng T, Sun D, Weng Q, Jia W, Shen W, Pu L, He J.
    Chin Med J (Engl); 1997 May; 110(5):372-8. PubMed ID: 9594306
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  • 53. Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic study.
    Burstedt MS, Ristoff E, Larsson A, Wachtmeister L.
    Ophthalmology; 2009 Feb; 116(2):324-31. PubMed ID: 19111905
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  • 54. 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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  • 56. Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation.
    Sue CM, Mitchell P, Crimmins DS, Moshegov C, Byrne E, Morris JG.
    Neurology; 1997 Oct; 49(4):1013-7. PubMed ID: 9339682
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  • 57. Comparison of nonmydriatic digital retinal imaging versus dilated ophthalmic examination for nondiabetic eye disease in persons with diabetes.
    Chow SP, Aiello LM, Cavallerano JD, Katalinic P, Hock K, Tolson A, Kirby R, Bursell SE, Aiello LP.
    Ophthalmology; 2006 May; 113(5):833-40. PubMed ID: 16650680
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  • 59. Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.
    Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE.
    Invest Ophthalmol Vis Sci; 2004 Jul; 45(7):2355-60. PubMed ID: 15223817
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  • 60. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
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