A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy
Author:
Publisher
Elsevier BV
Subject
General Medicine,Pediatrics, Perinatology and Child Health,Surgery
Reference21 articles.
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2. A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism;Nestorowicz;Diabetes,1997
3. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinism of infancy;Thomas;Science,1995
4. Genetics of neonatal hyperinsulinism;Glaser;Arch Dis Child,2000
5. Loss of functional KATP channels in pancreatic beta- cells causes persistent hyperinsulinemic hypoglycemia of infancy;Kane;Nature Medicine,1996
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