MENERI, MEGI
MENERI, MEGI
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Single Nucleotide SMN1 Variants in a Cohort of Individuals With Spinal Muscular Atrophy
2025 M. Rimoldi, F. Magri, M. Meneri, D. Gagliardi, V. Ada Sansone, E. Albamonte, L. Ottoboni, G.P. Comi, E. Mercuri, F.D. Tiziano, D. Ronchi, S. Corti
Qualitative assessment of thrombus permeability: Patients’, histopathological, radiological characteristics and outcomes
2024 M. Meneri, L. Caschera, G. Lopez, G. Platania, C. Luisa Bianchi, S. Bonato, G. Costamagna
Investigating the prevalence of MFN2 mutations in amyotrophic lateral sclerosis: insights from an Italian cohort
2024 E. Abati, D. Gagliardi, A. Manini, R. Del Bo, D. Ronchi, M. Meneri, F. Beretta, A. Sarno, F. Rizzo, E. Monfrini, A. Di Fonzo, M.T. Pellecchia, A. Brusati, V. Silani, G.P. Comi, A. Ratti, F. Verde, N. Ticozzi, S. Corti
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
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
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
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
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
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
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
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
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
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
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
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
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies
2023 G. Costamagna, S. Bonato, S. Corti, M. Meneri
Homozygous SOD1 Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian Family
2022 D. Gagliardi, M. Ahmadinejad, R. Del Bo, M. Meneri, G.P. Comi, S. Corti, D. Ronchi
Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes
2022 M. Rizzuti, V. Melzi, D. Gagliardi, D. Resnati, M. Meneri, L. Dioni, P. Masrori, N. Hersmus, K. Poesen, M. Locatelli, F. Biella, R. Silipigni, V. Bollati, N. Bresolin, G.P. Comi, P. Van Damme, M. Nizzardo, S. Corti