Diazoxide-Unresponsive Forms of Congenital Hyperinsulinism
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-02961-6_3
Reference48 articles.
1. Bellanne-Chantelot C, et al. ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism. J Med Genet. 2010;47:752–9. https://doi.org/10.1136/jmg.2009.075416 .
2. Snider KE, et al. Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. J Clin Endocrinol Metab. 2013;98:E355–63. https://doi.org/10.1210/jc.2012-2169 .
3. Nessa A, Rahman SA, Hussain K. Hyperinsulinemic hypoglycemia - the molecular mechanisms. Front Endocrinol (Lausanne). 2016;7:29. https://doi.org/10.3389/fendo.2016.00029 .
4. Li C, et al. Functional and metabolomic consequences of KATP channel inactivation in human islets. Diabetes. 2017;66:1901–13. https://doi.org/10.2337/db17-0029 .
5. Macmullen CM, et al. Diazoxide-unresponsive congenital hyperinsulinism in children with dominant mutations of the beta-cell sulfonylurea receptor SUR1. Diabetes. 2011;60:1797–804. https://doi.org/10.2337/db10-1631 .
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