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Human Molecular Genetics|February 25, 2016
ALS mouse model SOD1G93A displays early pathology of sensory small fibers associated to accumulation of a neurotoxic splice variant of peripherinJenny Sassone, Michela Taiana, Raffaella Lombardi, et al.
Journal of Materials Science. Materials in Medicine|December 31, 2022
Silk fibroin microgels as a platform for cell microencapsulationNina Bono, Giulio Saroglia, Stefania Marcuzzo, et al.
Journal of Cell Science|February 13, 2019
VAPB depletion alters neuritogenesis and phosphoinositide balance in motoneuron-like cells: relevance to VAPB-linked amyotrophic lateral sclerosisPaola Genevini, Maria Nicol Colombo, Rossella Venditti, et al.
Scientific Reports|November 13, 2025
Metabolic reprogramming in amyotrophic lateral sclerosis ependymal stem cells by FM19G11 nanotherapyMarco Cattaneo, Marcella Bonanomi, Cristina Chirizzi, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 6, 2024
FM19G11-loaded nanoparticles modulate energetic status and production of reactive oxygen species in myoblasts from ALS miceClaudia Malacarne, Eleonora Giagnorio, Cristina Chirizzi, et al.
International Journal of Molecular Sciences|March 11, 2023
MiR-146a in ALS: Contribution to Early Peripheral Nerve Degeneration and Relevance as Disease BiomarkerEleonora Giagnorio, Claudia Malacarne, Paola Cavalcante, et al.
Ebiomedicine|November 8, 2020
CXCL13/CXCR5 signalling is pivotal to preserve motor neurons in amyotrophic lateral sclerosisMaria Chiara Trolese, Alessandro Mariani, Mineko Terao, et al.
Frontiers in Neuroscience|February 9, 2026
MicroRNA profiling in post-mortem spinal cord of C9ORF72-related ALS patients reveals molecular pathways involved in motor neuron degenerationGiorgia Farinazzo, Eleonora Giagnorio, Matteo Marcuzzo, et al.
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