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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)

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Biomaterials 70, 115125

GCB Bioenergy 15(1):723 Zou W et al (2022) Extending BigSMILES to non-covalent bonds in supramolecular polymer assemblies

Early animal studies suggest this combination may lead to faster recovery times and improved structural integrity of repaired tissues