Genetic Heterogeneity in Familial Hyperinsulinism
Mechanisms of amino acid-stimulated insulin secretion in congenital hyperinsulinism
Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8
Mutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi Jews
Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities
Effect of feeding on growth hormone response to growth hormone-releasing hormone in polycystic ovarian syndrome: relation with body weight and hyperinsulinism
Sar1-GTPase-dependent ER exit of KATP channels revealed by a mutation causing congenital hyperinsulinism
Identification of the molecular dysfunction caused by glutamate dehydrogenase S445L mutation responsible for hyperinsulinism/hyperammonemia
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n.1. excessive secretion of the hormone insulin by the islet cells of the pancreas. 2. metabolic disturbance due to administration of too much insulin.
1. excessive secretion of the hormone insulin by the islet cells of the pancreas. 2. metabolic disturbance due to administration of too much insulin.
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