Cargando…
Spinocerebellar ataxia clinical trials: opportunities and challenges
The spinocerebellar ataxias (SCAs) are a group of dominantly inherited diseases that share the defining feature of progressive cerebellar ataxia. The disease process, however, is not confined to the cerebellum; other areas of the brain, in particular, the brainstem, are also affected, resulting in a...
Autores principales: | Brooker, Sarah M., Edamakanti, Chandrakanth Reddy, Akasha, Sara M., Kuo, Sheng‐Han, Opal, Puneet |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8283160/ https://www.ncbi.nlm.nih.gov/pubmed/34019331 http://dx.doi.org/10.1002/acn3.51370 |
Ejemplares similares
-
Reactive Bergmann glia play a central role in spinocerebellar ataxia inflammation via the JNK pathway
por: Edamakanti, Chandrakanth Reddy, et al.
Publicado: (2023) -
Differential effects of Wnt-β-catenin signaling in Purkinje cells and Bergmann glia in spinocerebellar ataxia type 1
por: Luttik, Kimberly, et al.
Publicado: (2022) -
VEGF ameliorates the ataxic phenotype in spinocerebellar ataxia type 1 (SCA1) mice
por: Cvetanovic, Marija, et al.
Publicado: (2011) -
Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias
por: Gan, Shi-Rui, et al.
Publicado: (2017) -
Vascular Risk Factors and Clinical Progression in Spinocerebellar Ataxias
por: Lo, Raymond Y., et al.
Publicado: (2015)