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
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
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
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
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
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
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
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
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
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
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies
2023 G. Costamagna, S. Bonato, S. Corti, M. Meneri
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
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
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
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
New Insights into Cerebral Vessel Disease Landscapes at Single-Cell Resolution: Pathogenetic and Therapeutic Perspectives
2022 M. Meneri, S. Bonato, D. Gagliardi, G.P. Comi, S. Corti
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects
2022 A. Brusati, A. Ratti, V. Pensato, S. Peverelli, D. Gentilini, E. Dalla Bella, M.N. Sorce, M. Meneri, D. Gagliardi, S. Corti, C. Gellera, G. Lauria Pinter, N. Ticozzi, V. Silani
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort
2022 V. Montano, P. Lopriore, F. Gruosso, V. Carelli, G.P. Comi, M. Filosto, C. Lamperti, T. Mongini, O. Musumeci, S. Servidei, P. Tonin, A. Toscano, G. Primiano, M.L. Valentino, S. Bortolani, S. Marchet, G. Ricci, A. Modenese, S. Cotti Piccinelli, B. Risi, M. Meneri, I.G. Arena, G. Siciliano, M. Mancuso
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