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Last Updated: 01/07/2026
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Found 4451 publications
Severe refractory hypoglycaemia in neonatal sepsis: clinical insights and management approach.
Journal: BMJ case reports
Published: December 15, 2025
Diazoxide and Continuous Glucose Monitoring as Treatment in a Neonate with Hyperinsulinemic Hypoglycemia due to HNF4A Mutation.
Journal: Journal of clinical research in pediatric endocrinology
Published: September 17, 2025
Combined Effects of Diazoxide and Moderate-Intensity Exercise on the Restoration of Redox Balance Post-Fatigue in Fast- and Slow-Twitch Skeletal Muscles of Hypertensive Rats.
Journal: Biology
Published: September 07, 2025
Pharmacological Actions of Potassium Channel Openers on Voltage-Gated Potassium Channels.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: July 31, 2025
Gut microbiota and metabolite changes in metastatic colorectal cancer via 16S rRNA and metabolomics.
Gut microbiota and metabolite changes in metastatic colorectal cancer via 16S rRNA and metabolomics.
Journal: World journal of gastrointestinal oncology
Published: July 08, 2025
Intracellular Calcium Changes Correlate with Mitochondrial Dynamics After Differential Modulation of KATP Channels in a Cellular Model of Parkinson's Disease.
Journal: Neurochemical research
Published: June 22, 2025
Identification and Rescue of Congenital Hyperinsulinism-Associated ABCC8 Mutations that Impair KATP Channel Trafficking.
Journal: bioRxiv : the preprint server for biology
Published: June 06, 2025
Pharmacological Preconditioning with Diazoxide Upregulates HCN4 Channels in the Sinoatrial Node of Adult Rat Cardiomyocytes.
Journal: International journal of molecular sciences
Published: May 19, 2025
Advances in Pharmacotherapy for Congenital Hyperinsulinism.
Journal: Paediatric drugs
Published: May 18, 2025
Real-world experience with the use of diazoxide among people living with congenital hyperinsulinism and their caregivers.
Journal: Frontiers in endocrinology
Published: May 13, 2025
Congenital hyperinsulinemic hypoglycaemia in a neonate: a rare homozygous ABCC8 gene mutation.
Journal: BMJ case reports
Published: May 11, 2025
Last Updated: 01/07/2026