MENERI, MEGI
MENERI, MEGI
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
Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease
2024 A. Hidalgo-Gutierrez, J. Shintaku, J. Ramon, E. Barriocanal-Casado, A. Pesini, R.P. Saneto, G. Garrabou, J.C. Milisenda, A. Matas-Garcia, L. Gort, O. Ugarteburu, Y. Gu, L. Koganti, T. Wang, S. Tadesse, M. Meneri, M. Sciacco, S. Wang, K. Tanji, M.S. Horwitz, M.O. Dorschner, M. Mansukhani, G.P. Comi, D. Ronchi, R. Marti, A. Ribes, F. Tort, M. Hirano
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
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients
2023 G. Ricci, F. Torri, A. Govoni, R. Chiappini, L. Manca, G. Vadi, S. Roccella, F. Magri, M. Meneri, F. Fassini, V. Vacchiano, S. Tomassini, N. Gironella, M. Coccia, G. Comi, R. Liguori, G. Siciliano
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
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
Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study
2023 A. Vicino, L. Bello, S. Bonanno, A. Govoni, F. Cerri, M. Ferraro, G. Capece, G. Gadaleta, M. Meneri, V. Vacchiano, G. Ricci, E. D'Errico, I. Tramacere, P. Banfi, S. Bortolani, R. Zanin, M.A. Maioli, M. Silvestrini, S.C. Previtali, A. Berardinelli, M. Turri, M. Coccia, R. Mantegazza, R. Liguori, M. Filosto, G. Siciliano, I.L. Simone, T. Mongini, G. Comi, E. Pegoraro, L. Maggi
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
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
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies
2023 G. Costamagna, S. Bonato, S. Corti, M. Meneri
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
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
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
NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients
2023 A. Manini, D. Gagliardi, M. Meneri, S. Antognozzi, R. Del Bo, G.P. Comi, S. Corti, D. Ronchi
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
Biallelic Variants in ENDOG Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions
2022 A. Nasca, A. Legati, M. Meneri, M.E. Ermert, C. Frascarelli, N. Zanetti, M. Garbellini, G.P. Comi, A. Catania, C. Lamperti, D. Ronchi, D. Ghezzi
Stathmins and Motor Neuron Diseases: Pathophysiology and Therapeutic Targets
2022 D. Gagliardi, E. Pagliari, M. Meneri, V. Melzi, F. Rizzo, G.P. Comi, S.P. Corti, M.M. Taiana, M. Nizzardo
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
2022 A. Manini, L. Caporali, M. Meneri, S. Zanotti, D. Piga, I.G. Arena, S. Corti, A. Toscano, G.P. Comi, O. Musumeci, V. Carelli, D. Ronchi
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis
2022 A. Manini, D. Gagliardi, M. Meneri, S. Antognozzi, R. Del Bo, C. Scaglione, G.P. Comi, S. Corti, D. Ronchi
Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression
2022 A. Manini, M. Meneri, C. Rodolico, S. Corti, A. Toscano, G.P. Comi, O. Musumeci, D. Ronchi