192 related articles for article (PubMed ID: 15807877)
1. 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; 62(4):458-65. PubMed ID: 15807877
[TBL] [Abstract][Full Text] [Related]
2. ABCC8 (SUR1) and KCNJ11 (KIR6.2) mutations in persistent hyperinsulinemic hypoglycemia of infancy and evaluation of different therapeutic measures.
Darendeliler F; Fournet JC; Baş F; Junien C; Gross MS; Bundak R; Saka N; Günöz H
J Pediatr Endocrinol Metab; 2002; 15(7):993-1000. PubMed ID: 12199344
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.
Tanizawa Y; Matsuda K; Matsuo M; Ohta Y; Ochi N; Adachi M; Koga M; Mizuno S; Kajita M; Tanaka Y; Tachibana K; Inoue H; Furukawa S; Amachi T; Ueda K; Oka Y
Diabetes; 2000 Jan; 49(1):114-20. PubMed ID: 10615958
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. Diazoxide-unresponsive congenital hyperinsulinism in children with dominant mutations of the β-cell sulfonylurea receptor SUR1.
Macmullen CM; Zhou Q; Snider KE; Tewson PH; Becker SA; Aziz AR; Ganguly A; Shyng SL; Stanley CA
Diabetes; 2011 Jun; 60(6):1797-804. PubMed ID: 21536946
[TBL] [Abstract][Full Text] [Related]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.
Otonkoski T; Ammälä C; Huopio H; Cote GJ; Chapman J; Cosgrove K; Ashfield R; Huang E; Komulainen J; Ashcroft FM; Dunne MJ; Kere J; Thomas PM
Diabetes; 1999 Feb; 48(2):408-15. PubMed ID: 10334322
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.
Huopio H; Reimann F; Ashfield R; Komulainen J; Lenko HL; Rahier J; Vauhkonen I; Kere J; Laakso M; Ashcroft F; Otonkoski T
J Clin Invest; 2000 Oct; 106(7):897-906. PubMed ID: 11018078
[TBL] [Abstract][Full Text] [Related]
12. Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism.
Park SE; Flanagan SE; Hussain K; Ellard S; Shin CH; Yang SW
Eur J Endocrinol; 2011 Jun; 164(6):919-26. PubMed ID: 21422196
[TBL] [Abstract][Full Text] [Related]
13. 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; 47(6):715-22. PubMed ID: 11228046
[TBL] [Abstract][Full Text] [Related]
14. Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.
Shyng SL; Ferrigni T; Shepard JB; Nestorowicz A; Glaser B; Permutt MA; Nichols CG
Diabetes; 1998 Jul; 47(7):1145-51. PubMed ID: 9648840
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Activating mutations in the ABCC8 gene in neonatal diabetes mellitus.
Babenko AP; Polak M; Cavé H; Busiah K; Czernichow P; Scharfmann R; Bryan J; Aguilar-Bryan L; Vaxillaire M; Froguel P
N Engl J Med; 2006 Aug; 355(5):456-66. PubMed ID: 16885549
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
