BORDONI, ANDREINA
BORDONI, ANDREINA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
CPPs-conjugated antisense nucleotides : a new therapeutic strategy for Spinal Muscular Atrophy symptomatic patients
2020 E. Pagliari, M. Bersani, M. Rizzuti, A. Bordoni, D. Saccomanno, N. Bresolin, G. Comi, S. Corti, M. Nizzardo
Cell Penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical model
2020 E. Pagliari, M. Bersani, M. Rizzuti, A. Bordoni, D. Saccomanno, H.M. Moulton, N. Bresolin, G.P. Comi, S. Corti, M. Nizzardo
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency
2020 D. Ronchi, E. Monfrini, S. Bonato, V. Mancinelli, C. Cinnante, S. Salani, A. Bordoni, P. Ciscato, F. Fortunato, M. Villa, A. Di Fonzo, S. Corti, N. Bresolin, G.P. Comi
CPPs-conjugated antisense nucleotides : a new therapeutic strategy for Spinal Muscular Atrophy symptomatic patients
2019 E. Pagliari, M. Bersani, M. Rizzuti, A. Bordoni, G. Comi, S. Corti, M. Nizzardo
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome
2019 G. Bitetto, D. Ronchi, S. Bonato, A. Pittaro, G.M. Compagnoni, A. Bordoni, S. Salani, E. Frattini, G. Lopez, F.M. Cribiù, S. Corti, G.P. Comi, N. Bresolin, A. Di Fonzo
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy
2019 E. Monfrini, L. Straniero, S. Bonato, G. Monzio Compagnoni, A. Bordoni, R. Dilena, P. Rinchetti, R. Silipigni, D. Ronchi, S. Corti, G.P. Comi, N. Bresolin, S. Duga, A. Di Fonzo
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons
2019 F. Rizzo, M. Nizzardo, S. Vashisht, E. Molteni, V. Melzi, M. Taiana, S. Salani, P. Santonicola, E. Di Schiavi, M. Bucchia, A. Bordoni, I. Faravelli, N. Bresolin, G.P. Comi, U. Pozzoli, S. Corti
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III mice
2018 S. Pagliarani, S. Lucchiari, G. Ulzi, M. Ripolone, R. Violano, F. Fortunato, A. Bordoni, S. Corti, M. Moggio, N. Bresolin, G.P. Comi
Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy
2018 G. Monzio Compagnoni, G. Kleiner, A. Bordoni, F. Fortunato, D. Ronchi, S. Salani, M. Guida, C. Corti, I. Pichler, C. Bergamini, R. Fato, M.T. Pellecchia, A. Vallelunga, F. Del Sorbo, A. Elia, C. Reale, B. Garavaglia, G. Mora, A. Albanese, F. Cogiamanian, G. Ardolino, N. Bresolin, S. Corti, G.P. Comi, C.M. Quinzii, A. Di Fonzo
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD)
2017 M. Ripolone, R. Violano, D. Ronchi, S. Mondello, A. Nascimbeni, I. Colombo, G. Fagiolari, A. Bordoni, F. Fortunato, V. Lucchini, S. Simona, M. Filosto, O. Musumeci, P. Tonin, T. Mongini, S. Previtali, L. Morandi, C. Angelini, M. Mora, M. Sandri, M. Sciacco, A. Toscano, G.P. Comi, M. Moggio
Genome-wide RNA-seq and proteomic analysis of motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease, partially rescued by riboflavin
2017 F. Rizzo, A. Ramirez, C. Compagnucci, S. Salani, V. Melzi, A. Bordoni, F. Fortunato, N. Bresolin, G.P. Comi, E. Bertini, M. Nizzardo, S. Corti
A de novo C19orf12 heterozygous mutation in a patient with MPAN
2017 E. Monfrini, V. Melzi, G. Buongarzone, G. Franco, D. Ronchi, R. Dilena, E. Scola, P. Vizziello, A. Bordoni, N. Bresolin, G.P. Comi, S. Corti, A. Di Fonzo
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype
2016 M. Nizzardo, C. Simone, F. Rizzo, G. Ulzi, A. Ramirez, M. Rizzuti, A. Bordoni, M. Bucchia, S. Gatti, N. Bresolin, G.P. Comi, S. Corti
Changes in whole-body oxygen consumption and skeletal muscle mitochondria during linezolid-induced lactic acidosis
2016 A. Protti, D. Ronchi, G. Bassi, F. Fortunato, A. Bordoni, T. Rizzuti, R. Fumagalli
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons
2016 F. Rizzo, D. Ronchi, S. Salani, M. Nizzardo, F. Fortunato, A. Bordoni, G. Stuppia, R. Del Bo, D. Piga, R. Fato, N. Bresolin, G.P. Comi, S. Corti
Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation
2016 I. Colombo, S. Pagliarani, S. Testolin, C.M. Cinnante, G. Fagiolari, P. Ciscato, A. Bordoni, F. Fortunato, F. Magri, S.C. Previtali, D. Velardo, M. Sciacco, G.P. Comi, M. Moggio
Morpholino antisense oligomer against SOD1 for amyotrophic lateral sclerosis therapy
2015 C. Simone, M. Nizzardo, F. Rizzo, G. Ulzi, A. Ramirez, M. Bucchia, A. Bordoni, G. Comi, S. Corti
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family
2015 I. Colombo, S. Pagliarani, S. Testolin, E. Salsano, L.M. Napoli, A. Bordoni, S. Salani, E. D'Adda, L. Morandi, L. Farina, F. Magri, M. Riva, A. Prelle, M. Sciacco, G.P. Comi, M. Moggio
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy
2015 M. Ripolone, D. Ronchi, R. Violano, D. Vallejo, G. Fagiolari, E. Barca, V. Lucchini, I. Colombo, L. Villa, A. Berardinelli, U. Balottin, L. Morandi, M. Mora, A. Bordoni, F. Fortunato, S. Corti, D. Parisi, A. Toscano, M. Sciacco, S. Di Mauro, G.P. Comi, M. Moggio
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature
2014 G. Remiche, D. Ronchi, F. Magri, C. Lamperti, A. Bordoni, M. Moggio, N. Bresolin, G.P. Comi