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Journal Abstract Search

230 related items for PubMed ID: 8603770

  • 21. Diabetes with mitochondrial gene tRNALYS mutation.
    Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K.
    Diabetes Care; 1994 Dec; 17(12):1428-32. PubMed ID: 7882812
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  • 23. Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K.
    Diabetologia; 1994 Aug; 37(8):818-25. PubMed ID: 7988784
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  • 25. Pancreatic beta-cell dysfunction as the primary genetic lesion in NIDDM. Evidence from studies in normal glucose-tolerant individuals with a first-degree NIDDM relative.
    Pimenta W, Korytkowski M, Mitrakou A, Jenssen T, Yki-Jarvinen H, Evron W, Dailey G, Gerich J.
    JAMA; 1995 Jun 21; 273(23):1855-61. PubMed ID: 7776502
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  • 26. Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects.
    Fukuda M, Nakano S, Imaizumi N, Kitazawa M, Nishizawa M, Kigoshi T, Uchida K.
    J Diabetes Complications; 1999 Jun 21; 13(5-6):277-83. PubMed ID: 10765002
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  • 28. A comparison of four methods for assessing in vivo beta-cell function in normal, obese and non-insulin-dependent diabetic man.
    Davis SN, Piatti PM, Monti L, Möller N, Ng LL, Coppack S, Antsiferov M, Brown MD, Alberti KG.
    Diabetes Res; 1992 Mar 21; 19(3):107-17. PubMed ID: 1286545
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  • 30. Diminished insulin and glucagon secretory responses to arginine in nondiabetic subjects with a mutation in the hepatocyte nuclear factor-4alpha/MODY1 gene.
    Herman WH, Fajans SS, Smith MJ, Polonsky KS, Bell GI, Halter JB.
    Diabetes; 1997 Nov 21; 46(11):1749-54. PubMed ID: 9356021
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  • 32. Primary pancreatic beta-cell secretory defect caused by mutations in glucokinase gene in kindreds of maturity onset diabetes of the young.
    Velho G, Froguel P, Clement K, Pueyo ME, Rakotoambinina B, Zouali H, Passa P, Cohen D, Robert JJ.
    Lancet; 1992 Aug 22; 340(8817):444-8. PubMed ID: 1354782
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  • 33. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec 22; 14(6):343-8. PubMed ID: 11853367
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  • 34. Characterisation of beta-cell dysfunction of impaired glucose tolerance: evidence for impairment of incretin-induced insulin secretion.
    Fritsche A, Stefan N, Hardt E, Häring H, Stumvoll M.
    Diabetologia; 2000 Jul 22; 43(7):852-8. PubMed ID: 10952457
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  • 35. Quantitative and qualitative differences in basal and glucose- and arginine-stimulated insulin secretion in healthy subjects and different stages of NIDDM.
    Ratheiser K, Reitgruber W, Komjati M, Bratusch-Marrain P, Vierhapper H, Waldhäusl WK.
    Acta Diabetol Lat; 1990 Jul 22; 27(3):197-213. PubMed ID: 2075783
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  • 37. 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 22; 110(5):372-8. PubMed ID: 9594306
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  • 38. Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion.
    Pimenta WP, Santos ML, Cruz NS, Aragon FF, Padovani CR, Gerich JE.
    Diabetes Metab; 2002 Dec 22; 28(6 Pt 1):468-76. PubMed ID: 12522327
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  • 39. Lilly Lecture 1994. The beta-cell in diabetes: from molecular genetics to clinical research.
    Polonsky KS.
    Diabetes; 1995 Jun 22; 44(6):705-17. PubMed ID: 7789637
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  • 40. Insulin and glucose levels and prevalence of glucose intolerance in pedigrees with multiple diabetic siblings.
    Elbein SC, Maxwell TM, Schumacher MC.
    Diabetes; 1991 Aug 22; 40(8):1024-32. PubMed ID: 1860554
    [Abstract] [Full Text] [Related]

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