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Glial progenitor cell-based treatment of the childhood leukodystrophies

The childhood leukodystrophies comprise a group of hereditary disorders characterized by the absence, malformation or destruction of myelin. These disorders share common clinical, radiological and pathological features, despite their diverse molecular and genetic etiologies. Oligodendrocytes and ast...

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Détails bibliographiques
Publié dans:Exp Neurol
Auteurs principaux: Osorio, M. Joana, Goldman, Steven A.
Format: Artigo
Langue:Inglês
Publié: 2016
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5340082/
https://ncbi.nlm.nih.gov/pubmed/27170209
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2016.05.010
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