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Marquard J, Palladino AA, Stanley CA, Mayatepek E, Meissner T (2011) Rare forms of congenital hyperinsulinism. <i>Semin Pediatr Surg<\/i> 20: 38-44.","DOI":"10.1053\/j.sempedsurg.2010.10.006"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Ledermann HM (1995) Is maturity onset diabetes at young age (MODY) more common in Europe than previously assumed? <i>Lancet<\/i> 345: 648.","DOI":"10.1016\/S0140-6736(95)90548-0"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Christesen HB, Tribble ND, Molven A, Siddiqui J, Sandal T, et al. (2008) Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterization of a novel GCK mutation. <i>Eur J Endocrinol <\/i>159: 27-34<i>.<\/i>","DOI":"10.1530\/EJE-08-0203"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Suchi M, MacMullen C, Thornton PS, Ganguly A, Stanley CA, et al. 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Yorifuji T, Kawakita R, Nagai S, Sugimine A, Doi H, et al. (2011) Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes. <i>J Clin Endocrinol Metab <\/i>96: E141-E145.","DOI":"10.1210\/jc.2010-1281"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, et al. (2013) Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism. <i>Eur J Endocrinol <\/i>168: 557-564.","DOI":"10.1530\/EJE-12-0673"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. Su C, Gong C, Sanger P, Li W, Wu D, et al. (2014) Long-term follow-up and mutation analysis of 27 Chinese cases of congenital hyperinsulinism. <i>Horm Res Paediatr<\/i> 81: 169-176.","DOI":"10.1159\/000356911"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23. Park SE, Flanagan SE, Hussain K, Ellard S, Shin CH, et al. (2011) Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism.<i> Eur J Endocrinol <\/i>164: 919-926.","DOI":"10.1530\/EJE-11-0160"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24. Stanley CA, Lieu YK, Hsu BY, Burlina AB, Greenberg CR, et al. (1998) Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. <i>N Engl J Med<\/i> 338: 1352-1357.","DOI":"10.1056\/NEJM199805073381904"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. MacMullen C, Fang J, Hsu BYL, Kelly A, de Lonlay-Debeney P, et al. 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