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22. Glucose intolerance and diabetes are observed in the long-term follow-up of nonpancreatectomized patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene. Gussinyer M; Clemente M; Cebrián R; Yeste D; Albisu M; Carrascosa A Diabetes Care; 2008 Jun; 31(6):1257-9. PubMed ID: 18339976 [TBL] [Abstract][Full Text] [Related]
23. Prematurity, macrosomia, hyperinsulinaemic hypoglycaemia and a dominant ABCC8 gene mutation. Khoriati D; Arya VB; Flanagan SE; Ellard S; Hussain K BMJ Case Rep; 2013 Apr; 2013():. PubMed ID: 23563683 [TBL] [Abstract][Full Text] [Related]
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27. Complex ABCC8 DNA variations in congenital hyperinsulinism: lessons from functional studies. Muzyamba M; Farzaneh T; Behe P; Thomas A; Christesen HB; Brusgaard K; Hussain K; Tinker A Clin Endocrinol (Oxf); 2007 Jul; 67(1):115-24. PubMed ID: 17466004 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Permanent neonatal diabetes caused by a novel mutation. Jain V; Flanagan SE; Ellard S Indian Pediatr; 2012 Jun; 49(6):486-8. PubMed ID: 22796691 [TBL] [Abstract][Full Text] [Related]
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32. 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]
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