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Disrupted iron metabolism in peritoneal fluid may induce oxidative stress in the peritoneal cavity of women with endometriosis

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Potential pharmacokinetic and pharmacodynamic interactions between PSYs and common disease-modifying therapies (DMTs)such as interferons, fingolimod, natalizumab, or ocrelizumabare entirely uncharacterized and represent a critical translational knowledge gap

As a direct by-product of this, an overexpression of the enzymes is observed, acting as a defence mechanism [46,47,48,49]