Infantile Hyperinsulinism Associated with Enteropathy, Deafness and Renal Tubulopathy: Clinical Manifestations of a Syndrome Caused by a Contiguous Gene Deletion Located on Chromosome 11p-Reference-Cited by-同舟云学术

Infantile Hyperinsulinism Associated with Enteropathy, Deafness and Renal Tubulopathy: Clinical Manifestations of a Syndrome Caused by a Contiguous Gene Deletion Located on Chromosome 11p

Published:2004-01 Issue:12 Volume:17 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Publisher

Walter de Gruyter GmbH

Subject

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

Link

https://www.degruyter.com/document/doi/10.1515/JPEM.2004.17.12.1613/pdf

Reference24 articles.

1. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion

2. Loss of functional KATP channels in pancreatic β–cells causes persistent hyperinsulinemic hypoglycemia of infancy

3. A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

4. Hyperinsulinism of infancy: towards an understanding of unregulated insulin release

5. Advances in Diagnosis and Treatment of Hyperinsulinism in Infants and Children

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1. Homozygous 11p15-p14 Deletion Syndrome;Genetic Syndromes;2024

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3. Transcriptome Analysis Identifies Candidate Genes and Signaling Pathways Associated With Feed Efficiency in Xiayan Chicken;Frontiers in Genetics;2021-03-17

4. Species-Dependent Heterophilic and Homophilic Cadherin Interactions in Intestinal Intermicrovillar Links;2020-09-02

5. Hypoglycemia: Assessment and Management;Brook's Clinical Pediatric Endocrinology;2010-04-14