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25. The insulin gene in diabetes. Pugliese A; Miceli D Diabetes Metab Res Rev; 2002; 18(1):13-25. PubMed ID: 11921414 [TBL] [Abstract][Full Text] [Related]
26. The "other" diabetes. Gebel E Diabetes Forecast; 2010 May; 63(5):46-8. PubMed ID: 20481073 [No Abstract] [Full Text] [Related]
27. Diabetes: 1 and 2, or one and the same? Progress with the accelerator hypothesis. Wilkin TJ Pediatr Diabetes; 2008 Jun; 9(3 Pt 2):23-32. PubMed ID: 18540866 [TBL] [Abstract][Full Text] [Related]
29. Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation. D'Amato E; Tammaro P; Craig TJ; Tosi A; Giorgetti R; Lorini R; Ashcroft FM Diabet Med; 2008 Jun; 25(6):651-6. PubMed ID: 18544102 [TBL] [Abstract][Full Text] [Related]
30. Monogenic forms of diabetes mellitus: an update. Vaxillaire M; Froguel P Endocrinol Nutr; 2009 Dec; 56 Suppl 4():26-9. PubMed ID: 20629227 [No Abstract] [Full Text] [Related]
31. [The pathogenesis of diabetes mellitus. Present concepts]. Beischer W MMW Munch Med Wochenschr; 1982 Oct; 124(39):853-4. PubMed ID: 6815497 [No Abstract] [Full Text] [Related]
32. Early onset diabetes mellitus. Tip or iceberg? Polychronakos C Pediatr Diabetes; 2004 Dec; 5(4):171-3. PubMed ID: 15601358 [No Abstract] [Full Text] [Related]
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34. Association between DNA-sequences flanking the insulin-gene and atherosclerosis. Nerup J; Mandrup-Poulsen T; Owerbach D; Johansen K; Ingerslev J; Hansen AT Acta Endocrinol Suppl (Copenh); 1985; 272():35-41. PubMed ID: 3914802 [No Abstract] [Full Text] [Related]
35. New diabetes-associated mutation. Stewart A Mol Med Today; 1995 Apr; 1(1):2. PubMed ID: 9415127 [No Abstract] [Full Text] [Related]
36. Maturity onset diabetes of the young (MODY) and early onset Type II diabetes are not caused by loss of imprinting at the transient neonatal diabetes (TNDM) locus. Shield J; Owen K; Robinson DO; Mackay D; Ellard S; Hattersley A; Temple IK Diabetologia; 2001 Jul; 44(7):924. PubMed ID: 11508282 [No Abstract] [Full Text] [Related]
37. Is human insulin imprinted? Haig D Nat Genet; 1994 May; 7(1):10. PubMed ID: 7993432 [No Abstract] [Full Text] [Related]
38. Familial Sotos syndrome caused by a novel missense mutation, C2175S, in NSD1 and associated with normal intelligence, insulin dependent diabetes, bronchial asthma, and lipedema. Zechner U; Kohlschmidt N; Kempf O; Gebauer K; Haug K; Engels H; Haaf T; Bartsch O Eur J Med Genet; 2009; 52(5):306-10. PubMed ID: 19545651 [TBL] [Abstract][Full Text] [Related]
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