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More advanced modalities, including scanning and transmission electron microscopy with immune-gold labeling, have provided ultrastructural insights into NETs' architecture

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For treatment of primary systemic carnitine deficiency, a genetic impairment of normal biosynthesis or utilization of levocarnitine from dietary sources, or for the treatment of secondary carnitine deficiency resulting from an inborn error of metabolism such as glutaric aciduria II, methyl malonic aciduria, propionic acidemia, and medium chain fatty acylCoA dehydrogenase deficiency

For many others, high-dose oral therapy restores stores over weeks to months