Surgical treatment of congenital hyperinsulinism: Results from 500 pancreatectomies in neonates and children-Reference-Cited by-同舟云学术

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Surgical treatment of congenital hyperinsulinism: Results from 500 pancreatectomies in neonates and children

Published:2019-01 Issue:1 Volume:54 Page:27-32
ISSN:0022-3468
Container-title:Journal of Pediatric Surgery
language:en
Short-container-title:Journal of Pediatric Surgery

Author:

Adzick N. Scott,De Leon Diva D.,States Lisa J.,Lord Katherine,Bhatti Tricia R.,Becker Susan A.,Stanley Charles A.

Funder

NIH

Goldsmith Foundation

Congenital Hyperinsulinism International

Publisher

Elsevier BV

Subject

General Medicine,Pediatrics, Perinatology and Child Health,Surgery

Reference40 articles.

1. A specialized team approach to diagnosis and medical versus surgical treatment of infants with congenital hyperinsulinism;Palladino;Semin Pediatr Surg,2011

2. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinism of infancy;Thomas;Science,1995

3. Loss of functional KATP channels in pancreatic beta-cells causes persistent hyperinsulinemic hypoglycemia of infancy;Kane;Nat Med,1996

4. Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia;Verkarre;J. Clin. Invest.,1998

5. High risk of diabetes and neurobehavioral deficits in individuals with surgically treated hyperinsulinism;Lord;J Clin Endocrinol Metab,2015

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