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Amyotrophic lateral sclerosis and the clinical potential of dexpramipexole
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that leads to progressive weakness from loss of motor neurons and death on average in less than 3 years after symptom onset. No clear causes have been found and just one medication, riluzole, extends survival. Researchers have ident...
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Dove Medical Press
2012
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| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3431958/ https://ncbi.nlm.nih.gov/pubmed/22956874 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TCRM.S21981 |
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