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The most common adverse effects reported were gastrointestinal symptoms that were mild to moderate in intensity and occurred during dose escalation (14) ( Table 1 )

This is where trial and error comes in

113 and supporting data (unprocessed western blots)

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Although urine, stool, or volatile samples can be collected in a non-invasive way, the time of elimination has an impact on the degradation of the microbial products, which may have an impact on the analysis (79)

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