Cell Replacement Therapy Improves Pathological Hallmarks in a Mouse Model of Leukodystrophy Vanishing White Matter

Stem cell therapy has great prospects for brain white matter disorders, including the genetically determined disorders called leukodystrophies. We focus on the devastating leukodystrophy vanishing white matter (VWM). Patients with VWM show severe disability and early death, and treatment options are...

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Detalles Bibliográficos
Autores principales: Dooves, Stephanie, Leferink, Prisca S., Krabbenborg, Sander, Breeuwsma, Nicole, Bots, Saskia, Hillen, Anne E.J., Jacobs, Gerbren, van der Knaap, Marjo S., Heine, Vivi M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411482/
https://www.ncbi.nlm.nih.gov/pubmed/30799272
http://dx.doi.org/10.1016/j.stemcr.2019.01.018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411482/
https://www.ncbi.nlm.nih.gov/pubmed/30799272
http://dx.doi.org/10.1016/j.stemcr.2019.01.018

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