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Journal Abstract Search

336 related items for PubMed ID: 14715863

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  • 3. [Congenital hyperinsulinism in newborn and infant].
    Giurgea I, Ribeiro MJ, Boddaert N, Touati G, Robert JJ, Saudubray JM, Jaubert F, Bellanné-Chantelot C, Brunelle F, Nihoul-Fékété C, de Lonlay P.
    Arch Pediatr; 2005 Nov; 12(11):1628-35. PubMed ID: 16198094
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  • 4. Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism.
    Suchi M, MacMullen CM, Thornton PS, Adzick NS, Ganguly A, Ruchelli ED, Stanley CA.
    Mod Pathol; 2006 Jan; 19(1):122-9. PubMed ID: 16357843
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  • 7. A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy.
    Adzick NS, Thornton PS, Stanley CA, Kaye RD, Ruchelli E.
    J Pediatr Surg; 2004 Mar; 39(3):270-5. PubMed ID: 15017536
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  • 10. Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.
    Verkarre V, Fournet JC, de Lonlay P, Gross-Morand MS, Devillers M, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.
    J Clin Invest; 1998 Oct 01; 102(7):1286-91. PubMed ID: 9769320
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  • 11. KATP channel mutations in congenital hyperinsulinism.
    Saint-Martin C, Arnoux JB, de Lonlay P, Bellanné-Chantelot C.
    Semin Pediatr Surg; 2011 Feb 01; 20(1):18-22. PubMed ID: 21185999
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  • 12. Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations.
    Grimberg A, Ferry RJ, Kelly A, Koo-McCoy S, Polonsky K, Glaser B, Permutt MA, Aguilar-Bryan L, Stafford D, Thornton PS, Baker L, Stanley CA.
    Diabetes; 2001 Feb 01; 50(2):322-8. PubMed ID: 11272143
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  • 13. The Knudson's two-hit model and timing of somatic mutation may account for the phenotypic diversity of focal congenital hyperinsulinism.
    Giurgea I, Sempoux C, Bellanné-Chantelot C, Ribeiro M, Hubert L, Boddaert N, Saudubray JM, Robert JJ, Brunelle F, Rahier J, Jaubert F, Nihoul-Fékété C, de Lonlay P.
    J Clin Endocrinol Metab; 2006 Oct 01; 91(10):4118-23. PubMed ID: 16882742
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  • 17. Carriers of an inactivating beta-cell ATP-sensitive K(+) channel mutation have normal glucose tolerance and insulin sensitivity and appropriate insulin secretion.
    Huopio H, Vauhkonen I, Komulainen J, Niskanen L, Otonkoski T, Laakso M.
    Diabetes Care; 2002 Jan 01; 25(1):101-6. PubMed ID: 11772909
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