NIZZARDO, MONICA
NIZZARDO, MONICA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
CSF transplantation of a specific iPSC-derived neural stem cell subpopulation ameliorates the disease phenotype in a mouse model of spinal muscular atrophy with respiratory distress type 1
2019-11-01 G. Forotti, M. Nizzardo, M. Bucchia, A. Ramirez, E. Trombetta, S. Gatti, N. Bresolin, G.P. Comi, S. Corti
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1)
2020-01-01 M.G.L. Perego, N. Galli, M. Nizzardo, A. Govoni, M. Taiana, N. Bresolin, G.P. Comi, S. Corti
Downregulation of glutamic acid decarboxylase in Drosophila TDP- 43-null brains provokes paralysis by affecting the organization of the neuromuscular synapses
2018-01-01 G. Romano, N. Holodkov, R. Klima, F. Grilli, C. Guarnaccia, M. Nizzardo, F. Rizzo, R. Garcia, F. Feiguin
Effect of combined systemic and local morpholino treatment on the spinal muscular atrophy δ7 mouse model phenotype
2014-01-01 M. Nizzardo, C. Simone, S. Salani, M. Ruepp, F. Rizzo, M. Ruggieri, C. Zanetta, S. Brajkovic, H.M. Moulton, O. Müehlemann, N. Bresolin, G.P. Comi, S. Corti
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model
2015-01-01 M. Nizzardo, C. Simone, F. Rizzo, S. Salani, P. Rinchetti, R. Del Bo, S. Dametti, K. Foust, B. Kaspar, N. Bresolin, G. Comi, S. Corti
Genetic correction of spinal muscular atrophy-induced pluripotent stem cells and motoneurons as a disease model and cell source for transplantation
2012-01-01 G. Riboldi, M. Nizzardo, M. Nardini, C. Simone, M. Falcone, D. Ronchi, C. Donadoni, S. Salani, F. Magri, F. Rizzo, M. Ranieri, A. Govoni, I. Faravelli, C. Zanetta, N. Bresolin, G.P. Comi, S. Corti
Genome-wide RNA-seq and proteomic analysis of motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease, partially rescued by riboflavin
2017-04-01 F. Rizzo, A. Ramirez, C. Compagnucci, S. Salani, V. Melzi, A. Bordoni, F. Fortunato, N. Bresolin, G.P. Comi, E. Bertini, M. Nizzardo, S. Corti
The mitochondrial disulfide relay system protein GFER is mutated in autosomal recessive myopathy with congenital cataract and COX deficiency.
2009-06-01 A. Di Fonzo, D. Ronchi, T. Lodi, E. Fassone, M. Tigano, C. Lamperti, S. Corti, A. Bordoni, F. Fortunato, M. Nizzardo, L. Napoli, C. Donadoni, S. Salani, M. Moggio, N. Bresolin, I. Ferrero, G.P. Comi
Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired
2022-01-27 M. Taiana, A. Govoni, S. Salani, N. Kleinschmidt, N. Galli, M. Saladini, S.B. Ghezzi, V. Melzi, M. Bersani, R. Del Bo, O. Muehlemann, E. Bertini, V. Sansone, E. Albamonte, S. Messina, F. Mari, E. Cesaroni, L. Porfiri, F.D. Tiziano, G.L. Vita, M. Sframeli, C. Bonanno, N. Bresolin, G. Comi, S. Corti, M. Nizzardo
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)
2014-01-01 C. Zanetta, G. Riboldi, M. Nizzardo, C. Simone, I. Faravelli, N. Bresolin, G.P. Comi, S. Corti
Motoneuron Transplantation Rescues the Phenotype of SMARD1 (Spinal Muscular Atrophy with Respiratory Distress Type 1)
2009-09-23 S. Corti, M. Nizzardo, M. Nardini, C. Donadoni, S. Salani, R. Del Bo, D. Papadimitriou, F. Locatelli, N. Mezzina, F. Gianni, N. Bresolin, G.P. Comi
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches
2015-01-01 M. Nizzardo, C. Simone, S. Dametti, S. Salani, G. Ulzi, S. Pagliarani, F. Rizzo, E. Frattini, F. Pagani, N. Bresolin, G. Comi, S. Corti
Therapeutic applications of the cell-penetrating HIV-1 Tat peptide
2015-01-01 M. Rizzuti, M. Nizzardo, C. Zanetta, A. Ramirez, S. Corti