| North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy E Mazzone, D Martinelli, A Berardinelli, S Messina, A D’Amico, G Vasco, ... Neuromuscular Disorders 20 (11), 712-716, 2010 | 255 | 2010 |
| SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy E Pegoraro, EP Hoffman, L Piva, BF Gavassini, S Cagnin, M Ermani, ... Neurology 76 (3), 219-226, 2011 | 251 | 2011 |
| Reliability of the North Star Ambulatory Assessment in a multicentric setting ES Mazzone, S Messina, G Vasco, M Main, M Eagle, A D’Amico, L Doglio, ... Neuromuscular Disorders 19 (7), 458-461, 2009 | 248 | 2009 |
| Functional changes in Duchenne muscular dystrophy A 12-month longitudinal cohort study E Mazzone, G Vasco, MP Sormani, Y Torrente, A Berardinelli, S Messina, ... Neurology 77 (3), 250-256, 2011 | 236 | 2011 |
| Prednisone/prednisolone and deflazacort regimens in the CINRG Duchenne Natural History Study L Bello, H Gordish-Dressman, LP Morgenroth, EK Henricson, T Duong, ... Neurology 85 (12), 1048-1055, 2015 | 216 | 2015 |
| Diagnostic and Prognostic Biomarkers in Amyotrophic Lateral Sclerosis: Neurofilament Light Chain Levels in Definite Subtypes of Disease A Gaiani, I Martinelli, L Bello, G Querin, M Puthenparampil, S Ruggero, ... JAMA neurology, 2017 | 198 | 2017 |
| DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study L Bello, LP Morgenroth, H Gordish-Dressman, EP Hoffman, ... Neurology 87 (4), 401-409, 2016 | 164 | 2016 |
| 24 Month Longitudinal Data in Ambulant Boys with Duchenne Muscular Dystrophy ES Mazzone, M Pane, MP Sormani, R Scalise, A Berardinelli, S Messina, ... PLOS ONE 8 (1), e52512, 2013 | 151 | 2013 |
| Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patients Y Hathout, RL Marathi, S Rayavarapu, A Zhang, KJ Brown, H Seol, ... Human molecular genetics 23 (24), 6458-6469, 2014 | 135 | 2014 |
| Genetic modifiers of ambulation in the cooperative international Neuromuscular research group Duchenne natural history study L Bello, A Kesari, H Gordish‐Dressman, A Cnaan, LP Morgenroth, ... Annals of neurology 77 (4), 684-696, 2015 | 132 | 2015 |
| Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophy M Pane, ES Mazzone, L Fanelli, R De Sanctis, F Bianco, S Sivo, ... Neuromuscular Disorders 24 (3), 201-206, 2014 | 125 | 2014 |
| Redefining phenotypes associated with mitochondrial DNA single deletion M Mancuso, D Orsucci, C Angelini, E Bertini, V Carelli, GP Comi, ... Journal of neurology 262 (5), 1301-1309, 2015 | 106 | 2015 |
| Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials J Diaz-Manera, R Fernandez-Torron, J LLauger, MK James, A Mayhew, ... J Neurol Neurosurg Psychiatry, jnnp-2017-317488, 2018 | 104 | 2018 |
| 6 minute walk test in Duchenne MD patients with different mutations: 12 month changes M Pane, ES Mazzone, MP Sormani, S Messina, GL Vita, L Fanelli, ... PloS one 9 (1), e83400, 2014 | 102 | 2014 |
| Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy L Bello, L Piva, A Barp, A Taglia, E Picillo, G Vasco, M Pane, SC Previtali, ... Neurology 79 (2), 159-162, 2012 | 98 | 2012 |
| Interpreting genetic variants in titin in patients with muscle disorders M Savarese, L Maggi, A Vihola, PH Jonson, G Tasca, L Ruggiero, L Bello, ... JAMA neurology, 2018 | 93 | 2018 |
| 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), 1, 2016 | 92 | 2016 |
| TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular Dystrophy AA Fiorillo, CR Heier, JS Novak, CB Tully, KJ Brown, K Uaesoontrachoon, ... Cell reports 12 (10), 1678-1690, 2015 | 89 | 2015 |
| The “Usual Suspects”: Genes for Inflammation, Fibrosis, Regeneration, and Muscle Strength Modify Duchenne Muscular Dystrophy L Bello, E Pegoraro Journal of clinical medicine 8 (5), 649, 2019 | 87 | 2019 |
| Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients G Querin, C Bertolin, E Da Re, M Volpe, G Zara, E Pegoraro, N Caretta, ... J Neurol Neurosurg Psychiatry, jnnp-2015-311305, 2015 | 82 | 2015 |
