CORTI, STEFANIA PAOLA
CORTI, STEFANIA PAOLA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Unleashing the potential of mRNA therapeutics for inherited neurological diseases
2024 E. Monfrini, G. Baso, D. Ronchi, M. Meneri, D. Gagliardi, L. Quetti, F. Verde, N. Ticozzi, A. Ratti, A. Di Fonzo, G.P. Comi, L. Ottoboni, S. Corti
Shaping the Neurovascular Unit Exploiting Human Brain Organoids
2024 M. Rizzuti, V. Melzi, L. Brambilla, L. Quetti, L. Sali, L. Ottoboni, M. Meneri, A. Ratti, F. Verde, N. Ticozzi, G.P. Comi, S. Corti, E. Abati
Case report: Clinical and molecular characterization of two siblings affected by Brody myopathy
2023 D. Velardo, S. Antognozzi, M. Rimoldi, S. Pagliarani, F. Cogiamanian, S. Barbieri, S. Corti, G.P. Comi, D. Ronchi
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy
2023 D. Ronchi, M. Garbellini, F. Magri, F. Menni, M. Meneri, M.F. Bedeschi, R. Dilena, V. Cecchetti, I. Picciolli, F. Furlan, V. Polimeni, S. Salani, L. Pezzoli, F. Fortunato, M. Bellini, D. Piga, M. Ripolone, S. Zanotti, L. Napoli, P. Ciscato, M. Sciacco, G. Mangili, F. Mosca, S. Corti, M. Iascone, G.P. Comi
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene
2023 S. Zanotti, M. Ripolone, L. Napoli, D. Velardo, S. Salani, P. Ciscato, S. Priori, D. Kukavica, A. Mazzanti, L. Diamanti, E. Vegezzi, M. Moggio, S. Corti, G. Comi, M. Sciacco
Genomic and transcriptomic advances in amyotrophic lateral sclerosis
2023 M. Rizzuti, L. Sali, V. Melzi, S. Scarcella, G. Costamagna, L. Ottoboni, L. Quetti, L. Brambilla, D. Papadimitriou, F. Verde, A. Ratti, N. Ticozzi, G.P. Comi, S. Corti, D. Gagliardi
Clinical and molecular features of patients with amyotrophic lateral sclerosis and SOD1 mutations: a monocentric study
2023 D. Gagliardi, P. Ripellino, M. Meneri, R. Del Bo, S. Antognozzi, G.P. Comi, C. Gobbi, A. Ratti, N. Ticozzi, V. Silani, D. Ronchi, S. Corti
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study
2023 I. Faravelli, D. Gagliardi, E. Abati, M. Meneri, J. Ongaro, F. Magri, V. Parente, L. Petrozzi, G. Ricci, F. Farè, G. Garrone, M. Fontana, D. Caruso, G. Siciliano, G.P. Comi, A. Govoni, S. Corti, L. Ottoboni
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2A
2023 F. Rizzo, S. Bono, M.D. Ruepp, S. Salani, L. Ottoboni, E. Abati, V. Melzi, C. Cordiglieri, S. Pagliarani, R. De Gioia, A. Anastasia, M. Taiana, M. Garbellini, S. Lodato, P. Kunderfranco, D. Cazzato, D. Cartelli, C. Lonati, N. Bresolin, G. Comi, M. Nizzardo, S. Corti
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies
2023 G. Costamagna, S. Bonato, S. Corti, M. Meneri
Lafora Disease: A Case Report and Evolving Treatment Advancements
2023 C.R. Ferrari Aggradi, M. Rimoldi, G. Romagnoli, D. Velardo, M. Meneri, D. Iacobucci, M. Ripolone, L. Napoli, P. Ciscato, M. Moggio, G.P. Comi, D. Ronchi, S. Corti, E. Abati
Identification of Novel Biomarkers of Spinal Muscular Atrophy and Therapeutic Response by Proteomic and Metabolomic Profiling of Human Biological Fluid Samples
2023 M. Meneri, E. Abati, D. Gagliardi, I. Faravelli, V. Parente, A. Ratti, F. Verde, N. Ticozzi, G.P. Comi, L. Ottoboni, S. Corti
Cognitive abnormalities in Becker muscular dystrophy: a mysterious link between dystrophin deficiency and executive functions
2023 L. Pezzoni, R. Brusa, T. Difonzo, F. Magri, D. Velardo, S. Corti, G.P. Comi, M.C. Saetti
The impact of upper motor neuron involvement on clinical features, disease progression and prognosis in amyotrophic lateral sclerosis
2023 E. Colombo, F. Gentile, A. Maranzano, A. Doretti, F. Verde, M. Olivero, D. Gagliardi, M. Faré, M. Meneri, B. Poletti, L. Maderna, S. Corti, M. Corbo, C. Morelli, V. Silani, N. Ticozzi
Regional spreading pattern is associated with clinical phenotype in amyotrophic lateral sclerosis
2023 A. Maranzano, F. Verde, E. Colombo, B. Poletti, A. Doretti, R. Bonetti, D. Gagliardi, M. Meneri, L. Maderna, S. Messina, S. Corti, C. Morelli, V. Silani, N. Ticozzi
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant
2023 M. Rimoldi, F. Magri, S. Antognozzi, M. Ripolone, S. Salani, D. Piga, L. Bertolasi, S. Zanotti, P. Ciscato, F. Fortunato, M. Moggio, S. Corti, G.P. Comi, D. Ronchi
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?
2023 M. Ricci, G. Cicala, A. Capasso, G. Coratti, S. Fiori, C. Cutrona, A. D'Amico, V.A. Sansone, C. Bruno, S. Messina, T. Mongini, M. Coccia, G. Siciliano, E. Pegoraro, R. Masson, M. Filosto, G.P. Comi, S. Corti, D. Ronchi, L. Maggi, M.G. D'Angelo, V. Vacchiano, C. Ticci, L. Ruggiero, L. Verriello, F.S. Ricci, A.L. Berardinelli, M.A. Maioli, M. Garibaldi, V. Nigro, S.C. Previtali, M.C. Pera, E. Tizzano, M. Pane, F.D. Tiziano, E. Mercuri
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls
2023 F. Magri, L. Napoli, M. Ripolone, P. Ciscato, M. Moggio, S. Corti, G.P. Comi, M. Sciacco, S. Zanotti
Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis
2023 E. Colombo, A. Doretti, F. Scheveger, A. Maranzano, G. Pata, D. Gagliardi, M. Meneri, S. Messina, F. Verde, C. Morelli, S. Corti, L. Maderna, V. Silani, N. Ticozzi
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes
2023 S. Zanotti, F. Magri, S. Salani, L. Napoli, M. Ripolone, D. Ronchi, F. Fortunato, P. Ciscato, D. Velardo, M.G. D'Angelo, F. Gualandi, V. Nigro, M. Sciacco, S. Corti, G.P. Comi, D. Piga