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To je dvod, pro jeho efekt ve studich pesahuje daleko za hranice gastrointestinlnho traktu, kde byl pvodn objeven

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Bourque, J., Kousnetsov, R

To date, studies have reported minimal adverse effects at typical research-level dosages

Oral administration significantly reduces bioavailability due to enzymatic degradation in the digestive tract

Model performance (goodness-of-fit and predictive ability) was assessed in the full testing set and in patients with independent (0-2) and dependent (3-5) mRS scores separately