Cargando…
Mitochondrial malfunction in vanishing white matter disease: a disease of the cytosolic translation machinery
Autor principal: | Elroy-Stein, Orna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696837/ https://www.ncbi.nlm.nih.gov/pubmed/29171421 http://dx.doi.org/10.4103/1673-5374.217329 |
Ejemplares similares
-
Poor Cerebral Inflammatory Response in eIF2B Knock-In Mice: Implications for the Aetiology of Vanishing White Matter Disease
por: Cabilly, Yuval, et al.
Publicado: (2012) -
Vanishing White Matter Disease in a Spanish Population
por: Turón-Viñas, Eulàlia, et al.
Publicado: (2014) -
Edaravone and mitochondrial transfer as potential therapeutics for vanishing white matter disease astrocyte dysfunction
por: Ng, Neville S., et al.
Publicado: (2023) -
A Promising Small Molecule for Vanishing White Matter Disease
por: Mithal, Divakar S., et al.
Publicado: (2018) -
Regional vulnerability of brain white matter in vanishing white matter
por: Man, Jodie H.K., et al.
Publicado: (2023)