Enteroinsular hormones in two siblings with Donohue syndrome and complete leptin deficiency-Reference-Cited by-同舟云学术

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Enteroinsular hormones in two siblings with Donohue syndrome and complete leptin deficiency

Published:2017-12-11 Issue:4 Volume:19 Page:675-679
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Güemes M¹²,Rahman SA¹²^ORCID,Shah P¹²,Hussain K¹³

Affiliation:

1. Genetics and Genomic Medicine Programme, Genetics and Epigenetics in Health and Disease Section; Institute of Child Health, University College London; London UK

2. Endocrinology Department; Great Ormond Street Hospital for Children NHS Trust; London UK

3. Division of Endocrinology, Department of Pediatric Medicine; Sidra Medical & Research Center; Doha Qatar

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pedi.12619/fullpdf

Reference17 articles.

1. Leprechaunism: an inherited defect in a high-affinity insulin receptor;Elsas;Am J Hum Genet,1985

2. Genotype-phenotype correlation in inherited severe insulin resistance;Longo;Hum Mol Genet,2002

3. Hypoglycemia and resistance to ketoacidosis in a subject without functional insulin receptors;Ogilvy-Stuart;J Clin Endocrinol Metab,2001

4. Entero-insular axis;Unger;Arch Intern Med,1969

5. Leptin suppression of insulin secretion by the activation of ATP-sensitive K+ channels in pancreatic beta-cells;Kieffer;Diabetes,1997

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