| Diagnosis, treatment and follow-up of the carpal tunnel syndrome: a review C Alfonso, S Jann, R Massa, A Torreggiani Neurological Sciences 31, 243-252, 2010 | 336 | 2010 |
| SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis A Orlacchio, C Babalini, A Borreca, C Patrono, R Massa, S Basaran, ... Brain 133 (2), 591-598, 2010 | 313 | 2010 |
| Loss and renewal of thick myofilaments in glucocorticoid‐treated rat soleus after denervation and reinnervation R Massa, S Carpenter, P Holland, G Karpati Muscle & Nerve: Official Journal of the American Association of …, 1992 | 131 | 1992 |
| Recommendations for anesthesia and perioperative management of patients with neuromuscular disorders F Racca, T Mongini, A Wolfler, A Vianello, R Cutrera, L Del Sorbo, ... Minerva Anestesiol 79 (4), 419-33, 2013 | 114 | 2013 |
| Differential features of muscle fiber atrophy in osteoporosis and osteoarthritis C Terracciano, M Celi, D Lecce, J Baldi, E Rastelli, E Lena, R Massa, ... Osteoporosis International 24, 1095-1100, 2013 | 109 | 2013 |
| ALS5/SPG11/ KIAA1840 mutations cause autosomal recessive axonal Charcot–Marie–Tooth disease C Montecchiani, L Pedace, T Lo Giudice, A Casella, M Mearini, ... Brain 139 (1), 73-85, 2016 | 105 | 2016 |
| MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients C Fiorillo, G Astrea, M Savarese, D Cassandrini, G Brisca, F Trucco, ... Orphanet journal of rare diseases 11, 1-14, 2016 | 92 | 2016 |
| LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population O Musumeci, G la Marca, M Spada, S Mondello, C Danesino, GP Comi, ... Journal of Neurology, Neurosurgery & Psychiatry 87 (1), 5-11, 2016 | 82 | 2016 |
| Sleep disorders in adult‐onset myotonic dystrophy type 1: a controlled polysomnographic study A Romigi, F Izzi, V Pisani, F Placidi, LR Pisani, MG Marciani, F Corte, ... European Journal of Neurology 18 (9), 1139-1145, 2011 | 81 | 2011 |
| Long-term outcome of thoracoscopic extended thymectomy for nonthymomatous myasthenia gravis E Pompeo, F Tacconi, R Massa, D Mineo, S Nahmias, TC Mineo European journal of cardio-thoracic surgery 36 (1), 164-169, 2009 | 80 | 2009 |
| Familial inclusion body myositis among Kurdish-Iranian Jews R Massa, B Weller, G Karpati, E Shoubridge, S Carpenter Archives of neurology 48 (5), 519-522, 1991 | 80 | 1991 |
| Screening of ARHSP‐TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion PS Denora, D Schlesinger, C Casali, F Kok, A Tessa, A Boukhris, ... Human mutation 30 (3), E500-E519, 2009 | 75 | 2009 |
| Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases VA Sansone, M Panzeri, M Montanari, G Apolone, S Gandossini, ... European Journal of Neurology 17 (9), 1178-1187, 2010 | 67 | 2010 |
| Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2 V Pisani, MB Panico, C Terracciano, E Bonifazi, G Meola, G Novelli, ... Muscle & Nerve: Official Journal of the American Association of …, 2008 | 67 | 2008 |
| Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1 A Perfetti, S Greco, R Cardani, B Fossati, G Cuomo, R Valaperta, ... Scientific reports 6 (1), 38174, 2016 | 65 | 2016 |
| Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients LB Salehi, E Bonifazi, ED Stasio, M Gennarelli, A Botta, L Vallo, R Iraci, ... Genetic testing 11 (1), 84-90, 2007 | 65 | 2007 |
| Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients EM Pennisi, M Arca, E Bertini, C Bruno, D Cassandrini, A D’amico, ... Orphanet journal of rare diseases 12, 1-10, 2017 | 60 | 2017 |
| Effect of the [CCTG] n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) A Botta, S Caldarola, L Vallo, E Bonifazi, D Fruci, F Gullotta, R Massa, ... Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1762 (3), 329-334, 2006 | 58 | 2006 |
| Italian recommendations for the diagnosis and treatment of myasthenia gravis A Evoli, G Antonini, C Antozzi, A DiMuzio, F Habetswallner, C Iani, ... Neurological Sciences 40, 1111-1124, 2019 | 53 | 2019 |
| Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy A Ruggieri, F Brancati, S Zanotti, L Maggi, MB Pasanisi, S Saredi, ... Acta neuropathologica communications 3, 1-14, 2015 | 53 | 2015 |
