FARAVELLI, IRENE
FARAVELLI, IRENE
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
SPINAL MUSCULAR ATROPHY ORGANOIDS REVEAL DEVELOPMENTAL DEFECTS RESCUED BY ANTISENSE OLIGONUCLEOTIDES TREATMENT
2023 I. Faravelli
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
Autophagy in lupus nephritis: A delicate balance between regulation and disease
2022 M.A. Podesta, I. Faravelli, C. Ponticelli
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
Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional study
2021 D. Gagliardi, I. Faravelli, M. Meneri, D. Saccomanno, A. Govoni, F. Magri, G. Ricci, G. Siciliano, G. Pietro Comi, S. Corti
Immunosuppression-related neurological disorders in kidney transplantation
2021 I. Faravelli, D. Velardo, M.A. Podestà, C. Ponticelli
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort Study
2021 D. Gagliardi, I. Faravelli, M.A. Podesta, R. Brusa, E. Mauri, D. Saccomanno, A. Di Fonzo, S. Bonato, E. Scarpini, N. Bresolin, G.P. Comi, S. Corti
Pediatric anti-HMGCR necrotizing myopathy: diagnostic challenges and literature review
2020 D. Velardo, I. Faravelli, C. Cinnante, M. Moggio, G.P. Comi
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature
2020 G. Costamagna, M. Meneri, E. Abati, R. Brusa, D. Velardo, D. Gagliardi, E. Mauri, C. Cinnante, N. Bresolin, G. Comi, S. Corti, I. Faravelli
Back to the origins : human brain organoids to investigate neurodegeneration
2020 I. Faravelli, G. Costamagna, S. Tamanini, S. Corti
Nusinersen treatment and cerebrospinal fluid neurofilaments : An explorative study on Spinal Muscular Atrophy type 3 patients
2020 I. Faravelli, M. Meneri, D. Saccomanno, D. Velardo, E. Abati, D. Gagliardi, V. Parente, L. Petrozzi, D. Ronchi, N. Stocchetti, E. Calderini, G. D'Angelo, G. Chidini, E. Prandi, G. Ricci, G. Siciliano, N. Bresolin, G.P. Comi, S. Corti, F. Magri, A. Govoni
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene
2020 R. Brusa, E. Mauri, L. Dell'Arti, F. Magri, D. Ronchi, V. Minorini, C. Mainetti, D. Gagliardi, I. Faravelli, M. Meneri, N. Bresolin, F. Viola, S. Corti, G.P. Comi
Spinal muscular atrophy — challenges in the therapeutic era
2020 I. Faravelli, S. Corti
iPSCs-Based Neural 3D Systems: A Multidimensional Approach for Disease Modeling and Drug Discovery
2019 G. Costamagna, L. Andreoli, S. Corti, I. Faravelli
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature
2019 D. Gagliardi, E. Mauri, F. Magri, D. Velardo, M. Meneri, E. Abati, R. Brusa, I. Faravelli, D. Piga, D. Ronchi, F. Triulzi, L. Peverelli, M. Sciacco, N. Bresolin, G.P. Comi, S. Corti, A. Govoni
Ophthalmoplegia due to Miller Fisher syndrome in a patient with myasthenia gravis
2019 R. Brusa, I. Faravelli, D. Gagliardi, F. Magri, F. Cogiamanian, D. Saccomanno, C. Cinnante, E. Mauri, E. Abati, N. Bresolin, S. Corti, G.P. Comi
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
Central nervous system involvement in common variable immunodeficiency: A case of acute unilateral optic neuritis in a 26 -year-old Italian Patient
2018 E. Abati, I. Faravelli, F. Magri, A. Govoni, D. Velardo, D. Gagliardi, E. Mauri, R. Brusa, N. Bresolin, G. Fabio, G.P. Comi, M.D.R. Carrabba, S. Corti
Exertional rhabdomyolysis leading to acute kidney injury: when genetic defects are diagnosed in adult life
2018 D. Cucchiari, I. Colombo, O. Amato, M.A. Podestà, F. Reggiani, R. Valentino, I. Faravelli, S. Testolin, M. Moggio, S. Badalamenti
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature
2018 D. Gagliardi, I. Faravelli, L. Villa, G. Pero, C. Cinnante, R. Brusa, E. Mauri, L. Tresoldi, F. Magri, A. Govoni, N. Bresolin, G.P. Comi, S. Corti