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Differential growth of human embryos in vitro: role of reactive oxygen species

Hereditary causes include genetic defects in the metabolism of amino acids, cholesterol, and fatty acids, such as propionyl-CoA carboxylase deficiency (aka propionic acidemia) and medium chain acyl-CoA dehydrogenase deficiency (36)

Furthermore, L-Carnitine also regulates the pool of acetyl-CoA, a key intermediary in energy metabolism processes [43]

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Hypothyroidism results in small dense LDL independent of IRS traits and hypertriglyceridemia

Siemes H, Nau H, Schultze K, Wittfoht W, Drews E, Penzien J, Seidel U: Valproate (VPA) metabolites in various clinical conditions of probable VPA-associated hepatotoxicity