• A mathematical analysis of adaptations to the metabolic fate of fructose in essential fructosuria subjects
• Doctor, my son is so tired... about a case of hereditary fructose intolerance
• Effect of dietary fructose on portal and systemic serum fructose levels in rats and in KHK-/- and GLUT5-/- mice
• Essential fructosuria (hepatic fructokinase deficiency)
• Expression, purification and preliminary crystallographic studies of human ketohexokinase
• Fructose-1,6-diphosphatase deficiency: a treatable neurometabolic disorder
• Fructosuria and recurrent hypoglycemia in a patient with a novel c.1693T>A variant in the 3' untranslated region of the aldolase B gene
• Fructosuria and recurrent hypoglycemia in a patient with a novel c.1693T>A variant in the 3' untranslated region of the aldolase B gene
• Fruit-induced FPIES masquerading as hereditary fructose intolerance
• Glucose/Fructose Delivery to the Distal Nephron Activates the Sodium-Chloride Cotransporter via the Calcium-Sensing Receptor
• Inborn Errors of Fructose Metabolism. What Can We Learn from Them?
• Ketohexokinase knockout mice, a model for essential fructosuria, exhibit altered fructose metabolism and are protected from diet-induced metabolic defects
• Prevalence and cardiometabolic correlates of ketohexokinase gene variants among UK Biobank participants
• Properties of normal and mutant recombinant human ketohexokinases and implications for the pathogenesis of essential fructosuria
• Screening Mentally Retarded Children for Inborn Errors of Metabolism
• Structures of alternatively spliced isoforms of human ketohexokinase