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It was originally studied for gastrointestinal healing but researchers quickly identified potent effects on connective tissue, tendons, ligaments, and joints

Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disorder caused by defects in hepatic glycoxidation metabolism, leading to excessive endogenous oxalate production

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Additionally, the influence of food processing, individual genetic variability, and the complex interactions between polyphenols and other dietary or environmental components on their absorption and bioactivity requires further exploration (120)