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DOI:10.1016/j.jaad.2013.07.044 [ Links ] 2
doi:10.1007/s40618-021-01624-2
Secondary carnitine deficiency can be caused by increased losses, pharmacological therapy, a number of inherited metabolic disorders [38], poor diet or malabsorption of carnitine, from increased renal tubular loss of free carnitine (Fanconi syndrome), haemodialysis, peritoneal dialysis, or the increased excretion of acylcarnitines[39] with certain drugs
16S rRNA sequencing identified microbiome changes, and LC-MS assessed striatal metabolite changes
Bioactivation of hexachlorobutadiene by glutathione conjugation
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