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Heritability studies suggest that genetic factors account for 2563% of the variability in serum UA levels

In contrast to an earlier study that also found such matched contralateral lesions (Werring et al., 2000), this more recent report detected such mirror precursory lesions well before a T2 lesion formed in the index hemisphere, precluding the previous explanation of axonal transection and Wallerian degeneration as a possible contributor to the contralateral mirror abnormality

Tyler et al

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Platelet-rich plasma activates proinflammatory signaling pathways and induces oxidative stress in tendon fibroblasts

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