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.
399 related articles for article (PubMed ID: 19254908)
1. 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]
2. Molecular mechanisms of neonatal hyperinsulinism. Giurgea I; Bellanné-Chantelot C; Ribeiro M; Hubert L; Sempoux C; Robert JJ; Blankenstein O; Hussain K; Brunelle F; Nihoul-Fékété C; Rahier J; Jaubert F; de Lonlay P Horm Res; 2006; 66(6):289-96. PubMed ID: 17003566 [TBL] [Abstract][Full Text] [Related]
3. Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell. Oçal G; Flanagan SE; Hacihamdioğlu B; Berberoğlu M; Siklar Z; Ellard S; Savas Erdeve S; Okulu E; Akin IM; Atasay B; Arsan S; Yağmurlu A J Pediatr Endocrinol Metab; 2011; 24(11-12):1019-23. PubMed ID: 22308858 [TBL] [Abstract][Full Text] [Related]
4. ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism. Bellanné-Chantelot C; Saint-Martin C; Ribeiro MJ; Vaury C; Verkarre V; Arnoux JB; Valayannopoulos V; Gobrecht S; Sempoux C; Rahier J; Fournet JC; Jaubert F; Aigrain Y; Nihoul-Fékété C; de Lonlay P J Med Genet; 2010 Nov; 47(11):752-9. PubMed ID: 20685672 [TBL] [Abstract][Full Text] [Related]
5. Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism. Kapoor RR; Flanagan SE; Arya VB; Shield JP; Ellard S; Hussain K Eur J Endocrinol; 2013 Apr; 168(4):557-64. PubMed ID: 23345197 [TBL] [Abstract][Full Text] [Related]
6. Hyperinsulinism in infancy--genetic aspects. Darendeliler F; Bas F Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():521-6. PubMed ID: 17551476 [TBL] [Abstract][Full Text] [Related]
7. [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 [TBL] [Abstract][Full Text] [Related]
8. The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy. Sandal T; Laborie LB; Brusgaard K; Eide SA; Christesen HB; Søvik O; Njølstad PR; Molven A Clin Genet; 2009 May; 75(5):440-8. PubMed ID: 19475716 [TBL] [Abstract][Full Text] [Related]
9. Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: clinical and functional characterization of two novel ABCC8 mutations. Faletra F; Snider K; Shyng SL; Bruno I; Athanasakis E; Gasparini P; Dionisi-Vici C; Ventura A; Zhou Q; Stanley CA; Burlina A Gene; 2013 Mar; 516(1):122-5. PubMed ID: 23266803 [TBL] [Abstract][Full Text] [Related]
10. Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations. Pinney SE; MacMullen C; Becker S; Lin YW; Hanna C; Thornton P; Ganguly A; Shyng SL; Stanley CA J Clin Invest; 2008 Aug; 118(8):2877-86. PubMed ID: 18596924 [TBL] [Abstract][Full Text] [Related]
11. 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 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Mutational analysis of ABCC8, KCNJ11, GLUD1, HNF4A and GCK genes in 30 Chinese patients with congenital hyperinsulinism. Sang Y; Xu Z; Liu M; Yan J; Wu Y; Zhu C; Ni G Endocr J; 2014; 61(9):901-10. PubMed ID: 25008049 [TBL] [Abstract][Full Text] [Related]
14. In vitro recovery of ATP-sensitive potassium channels in β-cells from patients with congenital hyperinsulinism of infancy. Powell PD; Bellanné-Chantelot C; Flanagan SE; Ellard S; Rooman R; Hussain K; Skae M; Clayton P; de Lonlay P; Dunne MJ; Cosgrove KE Diabetes; 2011 Apr; 60(4):1223-8. PubMed ID: 21411514 [TBL] [Abstract][Full Text] [Related]
15. KATP channel mutations in congenital hyperinsulinism. Saint-Martin C; Arnoux JB; de Lonlay P; Bellanné-Chantelot C Semin Pediatr Surg; 2011 Feb; 20(1):18-22. PubMed ID: 21185999 [TBL] [Abstract][Full Text] [Related]
16. Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. Faletra F; Athanasakis E; Morgan A; Biarnés X; Fornasier F; Parini R; Furlan F; Boiani A; Maiorana A; Dionisi-Vici C; Giordano L; Burlina A; Ventura A; Gasparini P Gene; 2013 May; 521(1):160-5. PubMed ID: 23506826 [TBL] [Abstract][Full Text] [Related]
17. The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism. Banerjee I; Skae M; Flanagan SE; Rigby L; Patel L; Didi M; Blair J; Ehtisham S; Ellard S; Cosgrove KE; Dunne MJ; Clayton PE Eur J Endocrinol; 2011 May; 164(5):733-40. PubMed ID: 21378087 [TBL] [Abstract][Full Text] [Related]
18. Congenital hyperinsulinism due to a compound heterozygous ABCC8 mutation with spontaneous resolution at eight weeks. Kumaran A; Kapoor RR; Flanagan SE; Ellard S; Hussain K Horm Res Paediatr; 2010; 73(4):287-92. PubMed ID: 20215776 [TBL] [Abstract][Full Text] [Related]
19. Congenital hyperinsulinism in Brazilian neonates: a study of histology, KATP channel genes, and proliferation of β cells. Lovisolo SM; Mendonça BB; Pinto EM; Manna TD; Saldiva PH; Zerbini MC Pediatr Dev Pathol; 2010; 13(5):375-84. PubMed ID: 20482375 [TBL] [Abstract][Full Text] [Related]