MAURI, ELEONORA
MAURI, ELEONORA
Universita' degli Studi di MILANO
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
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy
2021 D. Gagliardi, G. Costamagna, E. Abati, E. Mauri, R. Brusa, L. Scudeller, L. Andreoli, G. Citterio, E. Piccin, F. Magri, M. Meneri, D. Velardo, M. Sciacco, N. Bresolin, S. Corti, G.P. Comi
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies
2021 E. Mauri, D. Piga, A. Govoni, R. Brusa, S. Pagliarani, M. Ripolone, R. Dilena, C. Cinnante, M. Sciacco, D. Cassandrini, V. Nigro, N. Bresolin, S. Corti, G.P. Comi, F. Magri
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy
2021 E. Mauri, D. Piga, S. Pagliarani, F. Magri, A. Manini, M. Sciacco, M. Ripolone, L. Napoli, L. Borellini, C. Cinnante, D. Cassandrini, S. Corti, N. Bresolin, G.P. Comi, A. Govoni
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions
2021 M. Johari, J. Sarparanta, A. Vihola, P.H. Jonson, M. Savarese, M. Jokela, A. Torella, G. Piluso, E. Said, N. Vella, M. Cauchi, A. Magot, F. Magri, E. Mauri, C. Kornblum, J. Reimann, T. Stojkovic, N.B. Romero, H. Luque, S. Huovinen, P. Lahermo, K. Donner, G.P. Comi, V. Nigro, P. Hackman, B. Udd
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there?
2021 A.M. Pietroboni, S. Lanfranconi, A. Novella, T. Carandini, A. Arighi, E. Abati, R. Brusa, G. Costamagna, G. Lazzeri, E. Mauri, M. Pozzato, L. Sacchi, G. Valcamonica, D. Villa, S. Bonato, G.P. Comi, N. Bresolin, D. Galimberti, E. Scarpini, A. Nobili
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase
2020 E. Mauri, E. Abati, O. Musumeci, C. Rodolico, M.G. D'Angelo, M. Mirabella, M. Lucchini, L. Bello, E. Pegoraro, L. Maggi, L. Manneschi, C. Gemelli, M. Grandis, A. Zuppa, S. Massucco, L. Benedetti, C. Caponnetto, A. Schenone, A. Prelle, S.C. Previtali, M. Scarlato, A. D'Amico, E. Bertini, E.M. Pennisi, L. de Giglio, M. Pane, E. Mercuri, T. Mongini, F. Ricci, A. Berardinelli, G. Astrea, S. Lenzi, R. Battini, G. Ricci, F. Torri, G. Siciliano, F.M. Santorelli, A. Ariatti, M. Filosto, L. Passamano, L. Politano, M. Scutifero, P. Tonin, B. Fossati, C. Panicucci, C. Bruno, S. Ravaglia, M. Monforte, G. Tasca, E. Ricci, A. Petrucci, L. Santoro, L. Ruggiero, A. Barp, E. Albamonte, V. Sansone, D. Gagliardi, G. Costamagna, A. Govoni, F. Magri, R. Brusa, D. Velardo, M. Meneri, M. Sciacco, S. Corti, N. Bresolin, I. Moroni, S. Messina, A.D. Muzio, V. Nigro, R. Liguori, G. Antonini, A. Toscano, C. Minetti, 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
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
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
Acute flaccid paralysis due to Echovirus 30 in an immunosuppressed transplant recipient
2019 E. Mauri, A. Mastrangelo, S. Testa, L. Pellegrinelli, E. Pariani, S. Binda, F. Triulzi, S. Barbieri, C. Bana, G. Montini, R. Dilena
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies
2019 D. Piga, S. Salani, F. Magri, R. Brusa, E. Mauri, G.P. Comi, N. Bresolin, S. Corti
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
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: More than meets the eye
2018 E. Mauri, R. Dilena, A. Boccazzi, D. Ronchi, D. Piga, F. Triulzi, D. Gagliardi, R. Brusa, I. Faravelli, N. Bresolin, F. Magri, S. Corti, G.P. Comi
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
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