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Treatment for familial amyotrophic lateral sclerosis/motor neuron disease
BACKGROUND: Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND), is a rare neurodegenerative disease. Approximately 5% to 7% of ALS/MND patients report a family history of a similarly affected relative. Superoxide dismutase‐1 gene mutations are the cause in about 20% of fam...
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| Publicat a: | Cochrane Database Syst Rev |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley & Sons, Ltd
2009
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7388919/ https://ncbi.nlm.nih.gov/pubmed/19160266 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD006153.pub2 |
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