Profile of pridopidine and its potential in the treatment of Huntington disease: the evidence to date

Huntington disease (HD) is a chronic, genetic, neurodegenerative disease for which there is no cure. The main symptoms of HD are abnormal involuntary movements (chorea and dystonia), impaired voluntary movements (ie, incoordination and gait balance), progressive cognitive decline, and psychiatric di...

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Detalles Bibliográficos
Autores principales: Squitieri, Ferdinando, de Yebenes, Justo Garcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629959/
https://www.ncbi.nlm.nih.gov/pubmed/26604684
http://dx.doi.org/10.2147/DDDT.S65738

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629959/
https://www.ncbi.nlm.nih.gov/pubmed/26604684
http://dx.doi.org/10.2147/DDDT.S65738

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