Associated Papers
Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease.
Han B et al.
American Journal of Clinical Pathology, 2016
Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel.
Salisbury RJ et al.
Diabetes, 2015
25931474 (PubMed )
Supplement: supp_db14-1202_DB141202SupplementaryData1.pdf
Partial ABCC8 gene deletion mutations causing diazoxide-unresponsive hyperinsulinaemic hypoglycaemia.
Flanagan S et al.
Pediatric Diabetes, 2012
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism.
Banerjee I et al.
European Journal of Endocrinology, 2011
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