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Genetic basis The possibility of diagnosing multiple members from same family with CFS implies the contribution of genetic factors to CFS risk (Walsh et al

Tsimikas S, Kiechl S, Willeit J, Mayr M, Miller ER, Kronenberg F, Xu Q, Bergmark C, Weger S, Oberhollenzer F, Witztum JL

It is even better if its paired with a VITAMIN C injectable

Our DM villus model suggests CR-induced TSG function reduction/loss

Fluids Barriers CNS 2020, 17 (1), 69, DOI: 10.1186/s12987-020-00230-3Google Scholar13A blood-brain barrier overview on structure, function, impairment, and biomarkers of integrityKadry Hossam