Precision therapy for DEND (Developmental delay, Epilepsy and Neonatal Diabetes) syndrome in the era of genomics-Reference-Cited by-同舟云学术

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Precision therapy for DEND (Developmental delay, Epilepsy and Neonatal Diabetes) syndrome in the era of genomics

Published:2024-02 Issue: Volume: Page:
ISSN:0377-1237
Container-title:Medical Journal Armed Forces India
language:en
Short-container-title:Medical Journal Armed Forces India

Author:

Badal Sachendra^ORCID,Sondhi Vishal,Sannalli Kiran,Ram Mohan Karthik,Roy Shuvendu,Yadav Ashok K.,Kotwal Narendra

Publisher

Elsevier BV

Reference10 articles.

1. Activating mutations in the ABCC8 gene in neonatal diabetes mellitus;Babenko;N Engl J Med,2006

2. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy;Sagen;Diabetes,2004

3. Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism;Flanagan;Hum Mutat,2009

4. Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype;Flanagan;Diabetologia,2006

5. Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6. 2 mutations;Pearson;N Engl J Med,2006

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