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Thus, the presented personalized approach to the cumulative risk assessment for the development and correction of ADRs associated with an increase in the level of toxic VPA metabolites in the blood and urine allows clinicians to adapt previously known classical methods of treatment using valproate to individual patients from the standpoint of pharmacogenomics and pharmacometabolomics

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Non-alcoholic fatty liver disease in morbidly obese individuals undergoing bariatric surgery: prevalence and effect of the pre-bariatric very low calorie diet

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Effect of serotonergic anorectics on food intake and induction of Fos in brain of mice with disruption of melanocortin 3 and/or 4 receptors