These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. 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 [TBL] [Abstract][Full Text] [Related]
8. 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; 102(7):1286-91. PubMed ID: 9769320 [TBL] [Abstract][Full Text] [Related]
9. Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinism. Damaj L; le Lorch M; Verkarre V; Werl C; Hubert L; Nihoul-Fékété C; Aigrain Y; de Keyzer Y; Romana SP; Bellanne-Chantelot C; de Lonlay P; Jaubert F J Clin Endocrinol Metab; 2008 Dec; 93(12):4941-7. PubMed ID: 18796520 [TBL] [Abstract][Full Text] [Related]
10. Clinical and genetic heterogeneity in congenital hyperinsulinism. Meissner T; Mayatepek E Eur J Pediatr; 2002 Jan; 161(1):6-20. PubMed ID: 11808881 [TBL] [Abstract][Full Text] [Related]
11. The genetic basis of congenital hyperinsulinism. James C; Kapoor RR; Ismail D; Hussain K J Med Genet; 2009 May; 46(5):289-99. PubMed ID: 19254908 [TBL] [Abstract][Full Text] [Related]
12. Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene. Glaser B; Ryan F; Donath M; Landau H; Stanley CA; Baker L; Barton DE; Thornton PS Diabetes; 1999 Aug; 48(8):1652-7. PubMed ID: 10426386 [TBL] [Abstract][Full Text] [Related]
13. Hyperinsulinism of the newborn. Glaser B Semin Perinatol; 2000 Apr; 24(2):150-63. PubMed ID: 10805170 [TBL] [Abstract][Full Text] [Related]
14. Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity. Tornovsky S; Crane A; Cosgrove KE; Hussain K; Lavie J; Heyman M; Nesher Y; Kuchinski N; Ben-Shushan E; Shatz O; Nahari E; Potikha T; Zangen D; Tenenbaum-Rakover Y; de Vries L; Argente J; Gracia R; Landau H; Eliakim A; Lindley K; Dunne MJ; Aguilar-Bryan L; Glaser B J Clin Endocrinol Metab; 2004 Dec; 89(12):6224-34. PubMed ID: 15579781 [TBL] [Abstract][Full Text] [Related]
15. 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 [TBL] [Abstract][Full Text] [Related]
16. An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinism. Hussain K; Flanagan SE; Smith VV; Ashworth M; Day M; Pierro A; Ellard S Diabetes; 2008 Jan; 57(1):259-63. PubMed ID: 17942822 [TBL] [Abstract][Full Text] [Related]
17. Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy. Biagiotti L; Proverbio MC; Bosio L; Gervasi F; Rovida E; Cerioni V; Bove M; Valin PS; Albarello L; Zamproni I; Grassi S; Doglioni C; Mora S; Chiumello G; Biunno I Exp Mol Pathol; 2007 Aug; 83(1):59-64. PubMed ID: 17316607 [TBL] [Abstract][Full Text] [Related]
18. The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma. Sempoux C; Guiot Y; Dahan K; Moulin P; Stevens M; Lambot V; de Lonlay P; Fournet JC; Junien C; Jaubert F; Nihoul-Fekete C; Saudubray JM; Rahier J Diabetes; 2003 Mar; 52(3):784-94. PubMed ID: 12606521 [TBL] [Abstract][Full Text] [Related]
19. 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; 59(6):485-91. PubMed ID: 10189991 [TBL] [Abstract][Full Text] [Related]
20. Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism. Fournet JC; Mayaud C; de Lonlay P; Verkarre V; Rahier J; Brunelle F; Robert JJ; Nihoul-Fékété C; Saudubray JM; Junien C Horm Res; 2000; 53 Suppl 1():2-6. PubMed ID: 10895035 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]