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Journal Abstract Search

138 related items for PubMed ID: 10720932

  • 21. Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor.
    Thornton PS, MacMullen C, Ganguly A, Ruchelli E, Steinkrauss L, Crane A, Aguilar-Bryan L, Stanley CA.
    Diabetes; 2003 Sep; 52(9):2403-10. PubMed ID: 12941782
    [Abstract] [Full Text] [Related]

  • 22. Therapy for persistent hyperinsulinemic hypoglycemia of infancy. Understanding the responsiveness of beta cells to diazoxide and somatostatin.
    Kane C, Lindley KJ, Johnson PR, James RF, Milla PJ, Aynsley-Green A, Dunne MJ.
    J Clin Invest; 1997 Oct 01; 100(7):1888-93. PubMed ID: 9312191
    [Abstract] [Full Text] [Related]

  • 23. Genotypes of the pancreatic beta-cell K-ATP channel and clinical phenotypes of Japanese patients with persistent hyperinsulinaemic hypoglycaemia of infancy.
    Ohkubo K, Nagashima M, Naito Y, Taguchi T, Suita S, Okamoto N, Fujinaga H, Tsumura K, Kikuchi K, Ono J.
    Clin Endocrinol (Oxf); 2005 Apr 01; 62(4):458-65. PubMed ID: 15807877
    [Abstract] [Full Text] [Related]

  • 24. Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.
    Fournet JC, Verkarre V, De Lonlay P, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.
    Ann Endocrinol (Paris); 1998 Apr 01; 59(6):485-91. PubMed ID: 10189991
    [Abstract] [Full Text] [Related]

  • 25. An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus.
    Kukuvitis A, Deal C, Arbour L, Polychronakos C.
    J Clin Endocrinol Metab; 1997 Apr 01; 82(4):1192-4. PubMed ID: 9100595
    [Abstract] [Full Text] [Related]

  • 26. Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.
    Hussain K, Cosgrove KE, Shepherd RM, Luharia A, Smith VV, Kassem S, Gregory JW, Sivaprasadarao A, Christesen HT, Jacobsen BB, Brusgaard K, Glaser B, Maher EA, Lindley KJ, Hindmarsh P, Dattani M, Dunne MJ.
    J Clin Endocrinol Metab; 2005 Jul 01; 90(7):4376-82. PubMed ID: 15811927
    [Abstract] [Full Text] [Related]

  • 27. A new familial form of a late-onset, persistent hyperinsulinemic hypoglycemia of infancy caused by a novel mutation in KCNJ11.
    Yang YY, Long RK, Ferrara CT, Gitelman SE, German MS, Yang SB.
    Channels (Austin); 2017 Nov 02; 11(6):636-647. PubMed ID: 29087246
    [Abstract] [Full Text] [Related]

  • 28. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor.
    Dunne MJ, Kane C, Shepherd RM, Sanchez JA, James RF, Johnson PR, Aynsley-Green A, Lu S, Clement JP, Lindley KJ, Seino S, Aguilar-Bryan L.
    N Engl J Med; 1997 Mar 06; 336(10):703-6. PubMed ID: 9041101
    [No Abstract] [Full Text] [Related]

  • 29. From congenital hyperinsulinism to diabetes mellitus: the role of pancreatic beta-cell KATP channels.
    Hussain K, Cosgrove KE.
    Pediatr Diabetes; 2005 Jun 06; 6(2):103-13. PubMed ID: 15963039
    [Abstract] [Full Text] [Related]

  • 30. Compound heterozygosity for the common sulfonylurea receptor mutations can cause mild diazoxide-sensitive hyperinsulinism.
    Dekel B, Lubin D, Modan-Moses D, Quint J, Glaser B, Meyerovitch J.
    Clin Pediatr (Phila); 2002 Apr 06; 41(3):183-6. PubMed ID: 11999683
    [Abstract] [Full Text] [Related]

  • 31. Adenosine diphosphate as an intracellular regulator of insulin secretion.
    Nichols CG, Shyng SL, Nestorowicz A, Glaser B, Clement JP, Gonzalez G, Aguilar-Bryan L, Permutt MA, Bryan J.
    Science; 1996 Jun 21; 272(5269):1785-7. PubMed ID: 8650576
    [Abstract] [Full Text] [Related]

  • 32. A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism.
    Nestorowicz A, Inagaki N, Gonoi T, Schoor KP, Wilson BA, Glaser B, Landau H, Stanley CA, Thornton PS, Seino S, Permutt MA.
    Diabetes; 1997 Nov 21; 46(11):1743-8. PubMed ID: 9356020
    [Abstract] [Full Text] [Related]

  • 33. The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancy.
    Thomas PM, Cote GJ, Wohllk N, Mathew PM, Gagel RF.
    Proc Assoc Am Physicians; 1996 Jan 21; 108(1):14-9. PubMed ID: 8834059
    [Abstract] [Full Text] [Related]

  • 34. Persistent hyperinsulinemic hypoglycemia of infancy.
    Cohen MM.
    Am J Med Genet A; 2003 Nov 01; 122A(4):351-3. PubMed ID: 14518075
    [Abstract] [Full Text] [Related]

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  • 36. Sulfonylurea receptor 1 and Kir6.2 expression in the novel human insulin-secreting cell line NES2Y.
    Macfarlane WM, O'Brien RE, Barnes PD, Shepherd RM, Cosgrove KE, Lindley KJ, Aynsley-Green A, James RF, Docherty K, Dunne MJ.
    Diabetes; 2000 Jun 01; 49(6):953-60. PubMed ID: 10866047
    [Abstract] [Full Text] [Related]

  • 37. ATP-sensitive potassium channelopathies: focus on insulin secretion.
    Ashcroft FM.
    J Clin Invest; 2005 Aug 01; 115(8):2047-58. PubMed ID: 16075046
    [Abstract] [Full Text] [Related]

  • 38. 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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