Fructose malabsorption: causes, diagnosis and treatment, British Journal of Nutrition

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Gene variants of the SLC2A5 gene encoding GLUT5, the major fructose transporter, do not contribute to clinical presentation of acquired fructose malabsorption, BMC Gastroenterology

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Fructose malabsorption: causes, diagnosis and treatment, British Journal of Nutrition

Could Alzheimer's disease be a maladaptation of an evolutionary survival pathway mediated by intracerebral fructose and uric acid metabolism? - The American Journal of Clinical Nutrition

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The Malabsorption of Commonly Occurring Mono and Disaccharides (15.11.2013)

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PDF) Carbohydrate Malabsorption Syndromes and Early Signs of Mental Depression in Females

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