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PUBMED FOR HANDHELDS

Journal Abstract Search

336 related items for PubMed ID: 14715863

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  • 23. Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.
    Fournet JC, Mayaud C, de Lonlay P, Gross-Morand MS, Verkarre V, Castanet M, Devillers M, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.
    Am J Pathol; 2001 Jun; 158(6):2177-84. PubMed ID: 11395395
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  • 26. Histopathology of congenital hyperinsulinism: retrospective study with genotype correlations.
    Suchi M, MacMullen C, Thornton PS, Ganguly A, Stanley CA, Ruchelli ED.
    Pediatr Dev Pathol; 2003 Jun; 6(4):322-33. PubMed ID: 14692646
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  • 34. Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia.
    Flanagan SE, Kapoor RR, Banerjee I, Hall C, Smith VV, Hussain K, Ellard S.
    Clin Genet; 2011 Jun; 79(6):582-7. PubMed ID: 20573158
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  • 37. Partial ABCC8 gene deletion mutations causing diazoxide-unresponsive hyperinsulinaemic hypoglycaemia.
    Flanagan S, Damhuis A, Banerjee I, Rokicki D, Jefferies C, Kapoor R, Hussain K, Ellard S.
    Pediatr Diabetes; 2012 May; 13(3):285-9. PubMed ID: 21978130
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  • 40. Persistent hyperinsulinemic hypoglycemia of infancy.
    Cohen MM.
    Am J Med Genet A; 2003 Nov 01; 122A(4):351-3. PubMed ID: 14518075
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