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.
278 related articles for article (PubMed ID: 22876555)
1. 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]
2. 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]
3. Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation. Vieira TC; Bergamin CS; Gurgel LC; Moisés RS Pediatr Diabetes; 2010 Nov; 11(7):505-8. PubMed ID: 20042013 [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]
6. [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]
7. Successful treatment of congenital hyperinsulinism with long-acting release octreotide. Le Quan Sang KH; Arnoux JB; Mamoune A; Saint-Martin C; Bellanné-Chantelot C; Valayannopoulos V; Brassier A; Kayirangwa H; Barbier V; Broissand C; Fabreguettes JR; Charron B; Thalabard JC; de Lonlay P Eur J Endocrinol; 2012 Feb; 166(2):333-9. PubMed ID: 22048969 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
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. Prenatal diagnosis and postnatal management of diffuse congenital hyperinsulinism: a case report. Peranteau WH; Ganguly A; Steinmuller L; Thornton P; Johnson MP; Howell LJ; Stanley CA; Adzick NS Fetal Diagn Ther; 2006; 21(6):515-8. PubMed ID: 16969006 [TBL] [Abstract][Full Text] [Related]
13. 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]
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. An Egyptian case of congenital hyperinsulinism of infancy due to a novel mutation in KCNJ11 encoding Kir6.2 and response to octreotide. Sherif EM; Abdelmaksoud AA; Elbarbary NS; Njølstad PR Acta Diabetol; 2013 Oct; 50(5):801-5. PubMed ID: 20686794 [TBL] [Abstract][Full Text] [Related]
16. Efficacy and safety of long-term, continuous subcutaneous octreotide infusion for patients with different subtypes of KATP-channel hyperinsulinism. Yorifuji T; Kawakita R; Hosokawa Y; Fujimaru R; Matsubara K; Aizu K; Suzuki S; Nagasaka H; Nishibori H; Masue M Clin Endocrinol (Oxf); 2013 Jun; 78(6):891-7. PubMed ID: 23067144 [TBL] [Abstract][Full Text] [Related]
17. 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]
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. Sirolimus in the treatment of three infants with diffuse congenital hyperinsulinism. Al-Balwi R; Al-Atawi M; Al-Otaibi A; Babiker O; Al-Mutair A J Pediatr Endocrinol Metab; 2017 Aug; 30(9):1013-1017. PubMed ID: 28787272 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]