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Excessive glial cell activation, which induces extensive proinflammatory cytokine release, contributes to the development of neurodegenerative diseases [46]

Abstract Combined methylmalonic acidemia and homocystinuria, cblC type, is an inborn error of intracellular cobalamin metabolism with a wide spectrum of clinical manifestations that is stated to be the most common inherited disorder of cobalamin metabolism

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Similarly, O 2 radicals attack FeS centres in enzymes, making them inactive forever

However, we recommend following a balanced, nutritious diet to maximize the benefits of the medication and support overall health