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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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Foilsithe in:Exp Neurol
Main Authors: Osorio, M. Joana, Goldman, Steven A.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2016
Ábhair:
Rochtain Ar Líne: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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