BRUSA, ROBERTA
BRUSA, ROBERTA
Universita' degli Studi di MILANO
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature
2018 R. Brusa, F. Magri, D. Papadimitriou, A. Govoni, R. Del Bo, P. Ciscato, M. Savarese, C. Cinnante, M.C. Walter, A. Abicht, S. Bulst, S. Corti, M. Moggio, N. Bresolin, V. Nigro, 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
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
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
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
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
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
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
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
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
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
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases
2015 F. Magri, I. Colombo, R. Del Bo, S. Previtali, R. Brusa, P. Ciscato, M. Scarlato, D. Ronchi, M.G. D'Angelo, S. Corti, M. Moggio, N. Bresolin, G.P. Comi
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis
2020 F. Magri, R. Brusa, L. Bello, L. Peverelli, R.D. Bo, A. Govoni, C. Cinnante, I. Colombo, F. Fortunato, R. Tironi, S. Corti, N. Grimoldi, M. Sciacco, N. Bresolin, E. Pegoraro, M. Moggio, G.P. Comi
MicroRNAs as serum biomarkers in Becker muscular dystrophy
2022 D. Gagliardi, M. Rizzuti, R. Brusa, M. Ripolone, S. Zanotti, E. Minuti, V. Parente, L. Dioni, S. Cazzaniga, P. Bettica, N. Bresolin, G.P. Comi, S. Corti, F. Magri, D. Velardo
Noncoding RNAs in Duchenne and Becker muscular dystrophies: role in pathogenesis and future prognostic and therapeutic perspectives
2020 R. Brusa, F. Magri, N. Bresolin, G.P. Comi, S. Corti
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
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
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
The expanding spectrum of LAMA2 gene mutations : from congenital muscular dystrophy 1A to limb girdle muscular dystrophy 2R
2013 F. Magri, R. Del Bo, F. Fortunato, M. D’Angelo, A. Govoni, R. Brusa, S. Brajkovic, S. Corti, N. Bresolin, M. Moggio, G. Comi
The Italian limb girdle muscular dystrophy registry : relative frequency, clinical features, and differential diagnosis
2017 F. Magri, V. Nigro, C. Angelini, T. Mongini, M. Mora, I. Moroni, A. Toscano, M.G. D'Angelo, G. Tomelleri, G. Siciliano, G. Ricci, C. Bruno, S. Corti, O. Musumeci, G. Tasca, E. Ricci, M. Monforte, M. Sciacco, C. Fiorillo, S. Gandossini, C. Minetti, L. Morandi, M. Savarese, G. Di Fruscio, C. Semplicini, E. Pegoraro, A. Govoni, R. Brusa, R. Del Bo, D. Ronchi, M. Moggio, N. Bresolin, G.P. Comi