Recurrent spontaneous hypoglycaemia causes loss of neurogenic and neuroglycopaenic signs in infants with congenital hyperinsulinism
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2011.04250.x/fullpdf
Reference38 articles.
1. Non-insulinoma persistent hyperinsulinaemic hypoglycaemia caused by an activating glucokinase mutation: hypoglycaemia unawareness and attacks;Christesen;Clinical Endocrinology,2008
2. Congenital hyperinsulinism;Arnoux;Early Human Development,2010
3. A specialized team approach to diagnosis and medical versus surgical treatment of infants with congenital hyperinsulinism;Palladino;Seminars in Pediatric Surgery,2011
4. Mutations in the sulphonylurea receptor and familial persistent hyperinsulinemic hypoglycemia of infancy;Thomas;Science,1995
5. Mutation of the pancreatic islet inward rectifier, Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy;Thomas;Human Molecular Genetics,1996
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