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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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| I publikationen: | Cochrane Database Syst Rev |
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| Huvudupphovsmän: | , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
John Wiley & Sons, Ltd
2009
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| Länkar: | 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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