Cargando…
The neural substrates of Rapid-Onset Dystonia-Parkinsonism
Although dystonias are a common group of movement disorders the mechanisms by which brain dysfunction results in dystonia are not understood. Rapid-onset Dystonia-Parkinsonism is a hereditary dystonia caused by mutations in the ATP1A3 gene. Affected subjects can be symptom free for years but rapidly...
Autores principales: | Calderon, D. Paola, Fremont, Rachel, Kraenzlin, Franca, Khodakhah, Kamran |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430603/ https://www.ncbi.nlm.nih.gov/pubmed/21297628 http://dx.doi.org/10.1038/nn.2753 |
Ejemplares similares
-
A role for cerebellum in the hereditary dystonia DYT1
por: Fremont, Rachel, et al.
Publicado: (2017) -
Acute cerebellar knockdown of Sgce reproduces salient features of myoclonus-dystonia (DYT11) in mice
por: Washburn, Samantha, et al.
Publicado: (2019) -
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease
por: Hertz, Ellen, et al.
Publicado: (2023) -
A case of rapid-onset dystonia-parkinsonism accompanied by pyramidal tract impairment
por: Liu, Yanqiu, et al.
Publicado: (2016) -
An Elderly Woman with Reversal of Clinical Presentation Mimicking Rapid-Onset Dystonia-Parkinsonism
por: Ahn, Byoung June, et al.
Publicado: (2018)