Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1-Reference-Cited by-同舟云学术

Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1

Published:2000-10-01 Issue:7 Volume:106 Page:897-906
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Huopio Hanna,Reimann Frank,Ashfield Rebecca,Komulainen Jorma,Lenko Hanna-Liisa,Rahier Jaques,Vauhkonen Ilkka,Kere Juha,Laakso Markku,Ashcroft Frances,Otonkoski Timo

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference40 articles.

1. NESIDIOBLASTOSIS OF THE PANCREAS IN INFANCY

2. Persistent hyperinsulinaemic hypoglycaemia of infancy: therapy, clinical outcome and mutational analysis

3. Practical management of hyperinsulinism in infancy

4. Mutations in the Sulfonylurea Receptor Gene in Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy

Cited by 239 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The obesity-related mutation gene on nonalcoholic fatty liver disease;Human Genetics;2024-07-10

2. The Elusive Nature of ABCC8-related Maturity-Onset Diabetes of the Young (ABCC8-MODY). A Review of the Literature and Case Discussion;Current Diabetes Reports;2024-07-09

3. Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study;The Journal of Clinical Endocrinology & Metabolism;2024-07-04

4. Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemia;HISTOL HISTOPATHOL;2024

5. Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing;The CRISPR Journal;2024-02-01