138 related articles for article (PubMed ID: 18988933)
1. Case report: pathological features of aberrant pancreatic development in congenital hyperinsulinism due to ABCC8 mutations.
Brunetti-Pierri N; Olutoye OO; Heptulla R; Tatevian N
Ann Clin Lab Sci; 2008; 38(4):386-9. PubMed ID: 18988933
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) gene.
Thakur S; Flanagan SE; Ellard S; Verma IC
Indian Pediatr; 2011 Sep; 48(9):733-4. PubMed ID: 21992908
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A novel mutation associated with congenital hyperinsulinism.
Natarajan G; Aggarwal S; Merritt TA
Am J Perinatol; 2007 Aug; 24(7):401-4. PubMed ID: 17597441
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescue.
Yan FF; Lin YW; MacMullen C; Ganguly A; Stanley CA; Shyng SL
Diabetes; 2007 Sep; 56(9):2339-48. PubMed ID: 17575084
[TBL] [Abstract][Full Text] [Related]
10. 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; 6(4):322-33. PubMed ID: 14692646
[TBL] [Abstract][Full Text] [Related]
11. Severe congenital hyperinsulinism caused by a mutation in the Kir6.2 subunit of the adenosine triphosphate-sensitive potassium channel impairing trafficking and function.
Marthinet E; Bloc A; Oka Y; Tanizawa Y; Wehrle-Haller B; Bancila V; Dubuis JM; Philippe J; Schwitzgebel VM
J Clin Endocrinol Metab; 2005 Sep; 90(9):5401-6. PubMed ID: 15998776
[TBL] [Abstract][Full Text] [Related]
12. Mutation spectra of ABCC8 gene in Spanish patients with Hyperinsulinism of Infancy (HI).
Fernández-Marmiesse A; Salas A; Vega A; Fernández-Lorenzo JR; Barreiro J; Carracedo A
Hum Mutat; 2006 Feb; 27(2):214. PubMed ID: 16429405
[TBL] [Abstract][Full Text] [Related]
13. The causes of neonatal hypoglycemia.
Stanley CA; Baker L
N Engl J Med; 1999 Apr; 340(15):1200-1. PubMed ID: 10202173
[No Abstract] [Full Text] [Related]
14. Congenital hyperinsulinism: marked clinical heterogeneity in siblings with identical mutations in the ABCC8 gene.
Kapoor RR; Flanagan SE; Ellard S; Hussain K
Clin Endocrinol (Oxf); 2012 Feb; 76(2):312-3. PubMed ID: 21851374
[No Abstract] [Full Text] [Related]
15. 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]
16. Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation.
Baş VN; Ozkan M; Zenciroğlu A; Cavuşoğlu YH; Cetinkaya S; Aycan Z
J Pediatr Endocrinol Metab; 2012; 25(5-6):553-5. PubMed ID: 22876555
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinism.
Hussain K; Bryan J; Christesen HT; Brusgaard K; Aguilar-Bryan L
Diabetes; 2005 Oct; 54(10):2946-51. PubMed ID: 16186397
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genotype-phenotype associations in patients with severe hyperinsulinism of infancy.
Greer RM; Shah J; Jeske YW; Brown D; Walker RM; Cowley D; Bowling FG; Liaskou D; Harris M; Thomsett MJ; Choong C; Bell JR; Jack MM; Cotterill AM
Pediatr Dev Pathol; 2007; 10(1):25-34. PubMed ID: 17378627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
