| Literature DB >> 18668166 |
Chris Pierret1, Jason A Morrison, Mark D Kirk.
Abstract
Recent advances in our understanding of lysosomal storage disorders (LSDs) may lead to new therapies to treat the neuronal ceroid-lipofuscinoses (NCLs). In this review, enzyme replacement therapy, gene therapy, cell-mediated therapy and pharmaceutical treatments are considered across the LSDs and extended to therapies for the NCLs. It is likely that a combination of approaches will produce the most beneficial clinical outcome for treatment of pathologies displayed by the NCLs.Entities:
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Year: 2008 PMID: 18668166
Source DB: PubMed Journal: Acta Neurobiol Exp (Wars) ISSN: 0065-1400 Impact factor: 1.579