COMI, GIACOMO PIETRO
COMI, GIACOMO PIETRO
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
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
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
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
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies
2023 C. Dosi, A. Rubegni, J. Baldacci, D. Galatolo, S. Doccini, G. Astrea, A. Berardinelli, C. Bruno, G. Bruno, G.P. Comi, M.A. Donati, M.T. Dotti, M. Filosto, C. Fiorillo, F. Giannini, G.L. Gigli, M. Grandis, D. Lopergolo, F. Magri, M.A. Maioli, A. Malandrini, R. Massa, S. Matà, F. Melani, S. Messina, A. Mignarri, M. Moggio, E.M. Pennisi, E. Pegoraro, G. Ricci, M. Sacchini, A. Schenone, S. Sampaolo, M. Sciacco, G. Siciliano, G. Tasca, P. Tonin, R. Tupler, M. Valente, N. Volpi, D. Cassandrini, F.M. Santorelli
Tremulous spastic ataxia in a patient with a homozygous truncating SYNE1 variant
2023 F. Spagnolo, E. Monfrini, V. Pinto, G. Di Maggio, P. De Marco, G.P. Comi, A. Rini, A. Di Fonzo
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization
2023 M. Ripolone, S. Zanotti, L. Napoli, D. Ronchi, P. Ciscato, G.P. Comi, M. Moggio, 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
Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis
2023 G. Schwarz, S. Bonato, S. Lanfranconi, M. Matusevicius, I. Ghione, G. Valcamonica, G. Tsivgoulis, A. Paiva Nunes, M. Mancuso, A. Zini, P. Candelaresi, V. Rand, G.P. Comi, M.V. Mazya, N. Ahmed
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
Givinostat for Becker muscular dystrophy: A randomized, placebo-controlled, double-blind study
2023 G.P. Comi, E.H. Niks, K. Vandenborne, C.M. Cinnante, H.E. Kan, R.J. Willcocks, D. Velardo, F. Magri, M. Ripolone, J.J. van Benthem, N.M. van de Velde, S. Nava, L. Ambrosoli, S. Cazzaniga, P.U. Bettica
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
NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia
2023 F. Invernizzi, R. Izzo, I. Colangelo, A. Legati, N. Zanetti, B. Garavaglia, E. Lamantea, L. Peverelli, A. Ardissone, I. Moroni, L. Maggi, S. Bonanno, L. Fiori, D. Velardo, F. Magri, G.P. Comi, D. Ronchi, D. Ghezzi, C. Lamperti
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
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
Safety and efficacy of propranolol for treatment of familial cerebral cavernous malformations (Treat_CCM): a randomised, open-label, blinded-endpoint, phase 2 pilot trial
2023 S. Lanfranconi, E. Scola, J.M.T.A. Meessen, R. Pallini, G.A. Bertani, R. Al-Shahi Salman, E. Dejana, R. Latini, Giorgia Abete Fornara, M.A. Nicolò, A. Albanese, I. Awad, R. Bagnati, G. Balconi, E. Ballabio, E. Beghi, R. Bernasconi, A.B. Giulio, S. Besana, A. Blanda, C. Bossi, N. Bresolin, G.B. Maria, R. Calabrese, R.C. Maria, M. Castori, F.C. Elisa, R. Ciurleo, G.P. Comi, V. Contarino, G. Conte, L. D'Agruma, Q.D. Giorgio, Ugo de Grazia, Rina Di Bonaventura, P. D'Orio, G. Farago', A. Foresta, C. Fusco, C. Gaudino, G.L. Maria, A. Lanno, F. Lazzaroni, C. Lee, M. Locatelli, P.M. Aldo, P. Magnusson, M. Malinverno, M. Mangiavacchi, A. Mangraviti, S. Marino, S. Mazzola, B.N. Enrico, D. Novelli, L.O.F. Maria, A. Petracca, F. Pignotti, S. Pogliani, M. Poloni, A. Prelle, P. Raggi, F. Raucci, C. Regna-Gladin, D. Ronchi, E. Scelzo, S. Seyfried, A. Simeone, L.S. Carmelo, L. Tassi, M. Tettamanti, V. Torri, E. Tournier-Lasserve, R. Treglia, M.T. Fabio, C. Ungaro, E. Ursi, G. Valcamonica, A. Vasami', B. Zarino
Unraveling the Neurological Complexity of Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, and Skin Changes Syndrome: A Report of a Challenging Case of a Young Woman and Cutting-Edge Advancements in the Field
2023 G. Furciniti, G. Casalino, F.M. Lo Russo, N. Bolli, M. Meneri, G.P. Comi, S.P. Corti, D. Velardo
Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency
2023 E. Monfrini, A. Pesini, F. Biella, C.F.R. Sobreira, V. Emmanuele, G. Brescia, L.C. Lopez, S. Tadesse, M. Hirano, G.P. Comi, C.M. Quinzii, A. Di Fonzo
Verbal Learning Impairment in Parkinson's Disease: Role of the Frontostriatal System in Working and Strategic Memory
2023 A. Cocuzza, T. Difonzo, E.N. Aiello, L.P.E. Sbrissa, S. Zago, C. Gendarini, M.A. Sirtori, B. Poletti, N. Ticozzi, G. Franco, A. Di Fonzo, G.P. Comi, M.C. Saetti