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As mentioned above the only tedious thing was the filtering

Primary carnitine deficiency is a genetic disorder of the cellular carnitine delivery system that typically manifests around the age of five with symptoms of cardiomyopathy, skeletal muscle weakness and hypoglycemia

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[10] When a clinically significant carnitine deficiency is documented-such as in primary systemic carnitine deficiency, certain inborn errors of metabolism, or patients on chronic hemodialysis-injectable therapy is prescribed because it may restore blood and tissue levels more rapidly than oral supplements

Loss of acetylcholine leads to diminished attention span, blunted sensory perceptions, loss of arousal and structural changes in the synaptic junctions (the connections between neurons through which they communicate using chemical and electrical signals)