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A 6-week protocol requires roughly 4 to 5 vials
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Neurologically, ALD/AMN can manifest with highly variable phenotypes, ranging from very aggressive and rapidly fatal inflammatory CNS demyelination in young boys to a more slowly progressive adult form either with cerebral white matter inflammatory lesions, or a more indolent progressive myelopathy and peripheral neuropathy (Moser, 1997)
They might also be at risk of deficiency
[PubMed] [Google Scholar] 14.Brasaemle DL, Dolios G, Shapiro L, Wang R
