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Plasma Neurofilament Heavy Chain Levels Correlate to Markers of Late Stage Disease Progression and Treatment Response in SOD1(G93A) Mice that Model ALS

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disorder characterised by progressive degeneration of motor neurons leading to death, typically within 3–5 years of symptom onset. The diagnosis of ALS is largely reliant on clinical assessment and electrophysiological...

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Detalhes bibliográficos
Main Authors: Lu, Ching-Hua, Petzold, Axel, Kalmar, Bernadett, Dick, James, Malaspina, Andrea, Greensmith, Linda
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3397981/
https://ncbi.nlm.nih.gov/pubmed/22815892
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0040998
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