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Therapeutic interventions for disease progression in Huntington's disease

BACKGROUND: Huntington's disease (HD) is an autosomal dominant neurodegenerative disease with an average onset between the fourth and fifth decade of life; it leads to death 15 to 20 years after the onset of symptoms. Although several drugs seem effective in controlling the incapacitating manif...

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Detalhes bibliográficos
Publicado no:Cochrane Database Syst Rev
Main Authors: Mestre, Tiago, Ferreira, Joaquim, Coelho, Miguel M, Rosa, Mário, Sampaio, Cristina
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Ltd 2009
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7390161/
https://ncbi.nlm.nih.gov/pubmed/19588392
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD006455.pub2
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