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Journal Abstract Search

387 related items for PubMed ID: 23014256

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  • 22. Transient neonatal diabetes due to activating mutation in the ABCC8 gene encoding SUR1.
    Batra CM, Gupta N, Atwal G, Gupta V.
    Indian J Pediatr; 2009 Nov; 76(11):1169-72. PubMed ID: 20092027
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  • 24. Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
    Yokoi N, Kanamori M, Horikawa Y, Takeda J, Sanke T, Furuta H, Nanjo K, Mori H, Kasuga M, Hara K, Kadowaki T, Tanizawa Y, Oka Y, Iwami Y, Ohgawara H, Yamada Y, Seino Y, Yano H, Cox NJ, Seino S.
    Diabetes; 2006 Aug; 55(8):2379-86. PubMed ID: 16873704
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  • 32. Polymorphisms of the SUR1 (ABCC8) and Kir6.2 (KCNJ11) genes predict the conversion from impaired glucose tolerance to type 2 diabetes. The Finnish Diabetes Prevention Study.
    Laukkanen O, Pihlajamäki J, Lindström J, Eriksson J, Valle TT, Hämäläinen H, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Tuomilehto J, Uusitupa M, Laakso M, Finnish Diabetes Prevention Study Group.
    J Clin Endocrinol Metab; 2004 Dec; 89(12):6286-90. PubMed ID: 15579791
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  • 36. The molecular genetics of sulfonylurea receptors in the pathogenesis and treatment of insulin secretory disorders and type 2 diabetes.
    Lang V, Youssef N, Light PE.
    Curr Diab Rep; 2011 Dec; 11(6):543-51. PubMed ID: 21968738
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  • 37. A pathway to insulin independence in newborns and infants with diabetes.
    Shahawy S, Chan NK, Ellard S, Young E, Shahawy H, Mace J, Peverini R, Chinnock R, Njolstad PR, Hattersley AT, Hathout E.
    J Perinatol; 2011 Aug; 31(8):567-70. PubMed ID: 21796147
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  • 40. Three cases of permanent neonatal diabetes mellitus: genotypes and management outcome.
    Ooi HL, Wu LL.
    Singapore Med J; 2012 Jul; 53(7):e142-4. PubMed ID: 22815030
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