DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea
Author:
Affiliation:
1. Department of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center Children's Hospital, Seoul, Korea.
2. Medical Genetics Center, University of Ulsan College of Medicine, Asan Medical Center Children's Hospital, Seoul, Korea.
Funder
National Research Foundation of Korea
Publisher
Korean Academy of Medical Sciences
Subject
General Medicine
Link
https://synapse.koreamed.org/pdf/10.3346/jkms.2017.32.6.1042
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1. Maturity-onset diabetes of the young (MODY) - in search of ideal diagnostic criteria and precise treatment;Progress in Cardiovascular Diseases;2024-07
2. Precision therapy for DEND (Developmental delay, Epilepsy and Neonatal Diabetes) syndrome in the era of genomics;Medical Journal Armed Forces India;2024-02
3. Systematic Review of Monogenic Diabetes Prognostics;2023-05-21
4. Light-stimulated insulin secretion from pancreatic islet-like organoids derived from human pluripotent stem cells;Molecular Therapy;2023-05
5. Case report: Neonatal diabetes mellitus caused by KCNJ11 mutation presenting with intracranial hemorrhage;Frontiers in Neurology;2023-03-03
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