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Pharmacological Research|February 7, 2012
Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patientsMaria Grazia D'Angelo, Sandra Gandossini, Filippo Martinelli Boneschi, et al.
Journal of Alzheimer'S Disease : JAD|April 24, 2010
VEGF haplotypes are associated with increased risk to progressive supranuclear palsy and corticobasal syndromeBarbara Borroni, Roberto Del Bo, Stefano Goldwurm, et al.
Plos One|January 19, 2012
A functional variant in ERAP1 predisposes to multiple sclerosisFranca Rosa Guerini, Rachele Cagliani, Diego Forni, et al.
Brain : a Journal of Neurology|September 14, 2013
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Chiara Vantaggiato, Claudia Crimella, Giovanni Airoldi, et al.
Human Molecular Genetics|October 11, 2019
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove SyndromeGiacomo Bitetto, Dario Ronchi, Sara Bonato, et al.
Neurogenetics|July 14, 2009
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxinGiovanni Airoldi, Andrea Guidarelli, Orazio Cantoni, et al.
Muscle & Nerve|July 23, 2021
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, ItalyDelia Gagliardi, Gianluca Costamagna, Elena Abati, et al.
Neuroscience Letters|December 8, 2009
Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypesMilena De Riz, Daniela Galimberti, Chiara Fenoglio, et al.
Neurobiology of Aging|November 23, 2006
Absence of angiogenic genes modification in Italian ALS patientsRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
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