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Communicate with the School: The social aspect of this side effect can be devastating

Free Radic Res.2007;41(8):884-891

Bei pflanzenbasierter Ernhrung kann es hilfreich sein, L-Carnitin ber Nahrungsergnzungsmittel zuzufhren

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Primary carnitine deficiency or carnitine transporter defect is an autosomal recessive disorder of fatty acid oxidation caused by heterozygous mutations in the SLC22A5 gene that encodes the high-affinity carnitine transporter, OCTN2

oral administration of LAC leads to a significant increase in LAC concentrations in both plasma and cerebrospinal fluid (CSF) [33], showing that LAC crosses the bloodbrain barrier and reaches the brain at significant concentrations