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Autor:
Marco Milanese, Francesco Giribaldi, Marcello Melone, Tiziana Bonifacino, Ilaria Musante, Enrico Carminati, Pia I.A. Rossi, Laura Vergani, Adriana Voci, Fiorenzo Conti, Aldamaria Puliti, Giambattista Bonanno
Publikováno v:
Neurobiology of Disease, Vol 64, Iss , Pp 48-59 (2014)
Amyotrophic lateral sclerosis (ALS) is a late-onset fatal neurodegenerative disease reflecting degeneration of upper and lower motoneurons (MNs). The cause of ALS and the mechanisms of neuronal death are still largely obscure, thus impairing the esta
Externí odkaz:
https://doaj.org/article/09434e11a0ec4c4c8b31a83a803c68ef