ZANOLINI, ALICE
ZANOLINI, ALICE
Universita' degli Studi di MILANO
Patients on treatment with risdiplam in Italy: challenges in the interpretation of the real-world data
2025 E. Albamonte, A. Lizio, G. Coratti, L. Maggi, E. Pegoraro, M. Pane, S. Messina, R. Masson, A. D'Amico, E. Bertini, A. Pini, F. Ricci, T. Mongini, C. Bruno, K. Patanella, M. Sframeli, C. Dosi, S. Bonanno, G. Scarpini, N. Brolatti, A. Zanolini, C. Bravetti, M. Carmela Pera, E. Maria Mercuri, V.A.M. Sansone, Itasmac
Balance impairment in myotonic dystrophy type 1: Dynamic posturography suggests the coexistence of a proprioceptive and vestibular deficit
2022 S. Scarano, V.A. Sansone, C.R. Ferrari Aggradi, E. Carraro, L. Tesio, M. Amadei, V. Rota, A. Zanolini, A. Caronni
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy
2015 A. Reyes, L. Melchionda, A. Nasca, F. Carrara, E. Lamantea, A. Zanolini, C. Lamperti, M. Fang, J. Zhang, D. Ronchi, S. Bonato, G. Fagiolari, M. Moggio, D. Ghezzi, M. Zeviani
Redefining clinical phenotype in a large color of Italian non-dystrophic myotonic patients.
2009 V.A. Sansone, S. Lucchiari, A. Zanolini, S. Pagliarani, B. Fossati, M. Panzeri, S. Corti, F. Magri, N. Bresolin, G.P. Comi, G. Meola
Long-term follow-up free of ventricular fibrillation recurrence after resuscitated cardiac arrest in a myotonic dystrophy type 1 patient
2009 V. Sansone, G. De Ambroggi, A. Zanolini, M. Panzeri, F. Sardanelli, R. Cappato, G. Meola, L. De Ambroggi
Myotonia permanens with neonatal onset associated with a p.Gly1306Glu mutation in the SCN4A gene.
2009 V. Sansone, S. Pagliarani, S. Lucchiari, A. Zanolini, B. Fossati, M.C. Panzeri, G.P. Comi, G. Meola