RINCHETTI, PAOLA
RINCHETTI, PAOLA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Brain Calcifications: Genetic, Molecular, and Clinical Aspects
2023 E. Monfrini, F. Arienti, P. Rinchetti, F. Lotti, G.M. Riboldi
Sumoylation regulates the assembly and activity of the SMN complex
2021 G.M. Riboldi, I. Faravelli, T. Kuwajima, N. Delestree, G. Dermentzaki, M. De Planell-Saguer, P. Rinchetti, L.T. Hao, C.C. Beattie, S. Corti, S. Przedborski, G.Z. Mentis, F. Lotti
DEVELOPMENT OF 3D IN VITRO MODEL TO STUDY MOLECULAR MECHANISMS OF SPINAL MUSCULAR ATROPHY
2020 P. Rinchetti
Optimization of AAV9 gene therapy for Spinal Muscular Atrophy with respiratory distress Type 1 using in vivo disease models
2020 E. Pagliari, P. Rinchetti, N. Galli, S. Ghezzi, M. Taiana, G. Comi, S. Corti, M. Nizzardo
Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow
2020 V. Mishra, D.B. Re, V. Le Verche, M.J. Alvarez, A. Vasciaveo, A. Jacquier, P. Doulias, T.M. Greco, M. Nizzardo, D. Papadimitriou, T. Nagata, P. Rinchetti, E.J. Perez-Torres, K.A. Politi, B. Ikiz, K. Clare, M.E. Than, S. Corti, H. Ischiropoulos, F. Lotti, A. Califano, S. Przedborski
SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation
2020 P. Richard, S. Feng, Y.-. Tsai, W. Li, P. Rinchetti, U. Muhith, J. Irizarry-Cole, K. Stolz, L.A. Sanz, S. Hartono, M. Hoque, S. Tadesse, H. Seitz, F. Lotti, M. Hirano, F. Chedin, B. Tian, J.L. Manley
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
MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis
2017 P. Rinchetti, M. Rizzuti, I. Faravelli, S. Corti
Peptide-conjugated Morpholino Oligomers for treatment of Spinal Muscular Atrophy
2016 A. Ramirez, M. Rizzuti, F. Rizzo, P. Rinchetti, M. Bucchia, N. Bresolin, G.P. Comi, S. Corti, M. Nizzardo
Is spinal muscular atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications?
2016 C. Simone, A. Ramirez, M. Bucchia, P. Rinchetti, H. Rideout, D. Papadimitriou, D.B. Re, S. Corti
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model
2015 M. Nizzardo, C. Simone, F. Rizzo, S. Salani, P. Rinchetti, R. Del Bo, S. Dametti, K. Foust, B. Kaspar, N. Bresolin, G. Comi, S. Corti
Clinical and molecular features and therapeutic perspectives of spinal muscular atrophy with respiratory distress type 1
2015 F. Vanoli, P. Rinchetti, F. Porro, V. Parente, S. Corti
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model
2015 M. Nizzardo, C. Simone, F. Rizzo, S. Salani, S. Dametti, P. Rinchetti, R. Del Bo, K. Foust, B.K. Kaspar, N. Bresolin, G.P. Comi, S. Corti
Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives
2014 I. Faravelli, M. Bucchia, P. Rinchetti, M. Nizzardo, C. Simone, E. Frattini, S. Corti
The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review
2014 F. Porro, P. Rinchetti, F. Magri, G. Riboldi, M. Nizzardo, C. Simone, C. Zanetta, I. Faravelli, S. Corti