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Journal Abstract Search

248 related items for PubMed ID: 9312191

  • 1. 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
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  • 3. 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 01; 41(3):183-6. PubMed ID: 11999683
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  • 5. Congenital hyperinsulinism: molecular basis of a heterogeneous disease.
    Meissner T, Beinbrech B, Mayatepek E.
    Hum Mutat; 1999 Apr 01; 13(5):351-61. PubMed ID: 10338089
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  • 6. Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
    Sharma N, Crane A, Gonzalez G, Bryan J, Aguilar-Bryan L.
    Kidney Int; 2000 Mar 01; 57(3):803-8. PubMed ID: 10720932
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  • 7. Molecular biology of adenosine triphosphate-sensitive potassium channels.
    Aguilar-Bryan L, Bryan J.
    Endocr Rev; 1999 Apr 01; 20(2):101-35. PubMed ID: 10204114
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  • 9. Successful therapy with calcium channel blocker (nifedipine) in persistent neonatal hyperinsulinemic hypoglycemia of infancy.
    Baş F, Darendeliler F, Demirkol D, Bundak R, Saka N, Günöz H.
    J Pediatr Endocrinol Metab; 1999 Apr 01; 12(6):873-8. PubMed ID: 10614546
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  • 10. Characterization of genes encoding the pancreatic beta-cell ATP-sensitive K+ channel in persistent hyperinsulinemic hypoglycemia of infancy in Japanese patients.
    Someya T, Miki T, Sugihara S, Minagawa M, Yasuda T, Kohno Y, Seino S.
    Endocr J; 2000 Dec 01; 47(6):715-22. PubMed ID: 11228046
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  • 15. 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
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  • 16. Preoperative use of octreotide in a newborn with persistent hyperinsulinemic hypoglycemia of infancy.
    Apak RA, Yurdakök M, Oran O, Senocak ME, Cağlar M.
    J Pediatr Endocrinol Metab; 1998 Mar 02; 11 Suppl 1():143-5. PubMed ID: 9642652
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  • 17. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy.
    Thomas P, Ye Y, Lightner E.
    Hum Mol Genet; 1996 Nov 02; 5(11):1809-12. PubMed ID: 8923010
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  • 18. 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 02; 82(4):1192-4. PubMed ID: 9100595
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