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A multicenter, double‐blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophy MD Bonifati, G Ruzza, P Bonometto, A Berardinelli, K Gorni, S Orcesi, ... Muscle & nerve 23 (9), 1344-1347, 2000 | 262 | 2000 |
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 | 242 | 2010 |
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 | 234 | 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 | 229 | 2011 |
Effects of different ventilator settings on sleep and inspiratory effort in patients with neuromuscular disease F Fanfulla, M Delmastro, A Berardinelli, NDA Lupo, S Nava American journal of respiratory and critical care medicine 172 (5), 619-624, 2005 | 203 | 2005 |
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy E Mercuri, E Bertini, S Messina, A Solari, A D'amico, C Angelozzi, ... Neurology 68 (1), 51-55, 2007 | 202 | 2007 |
Autoantibodies to nodal isoforms of neurofascin in chronic inflammatory demyelinating polyneuropathy E Delmont, C Manso, L Querol, A Cortese, A Berardinelli, A Lozza, ... Brain 140 (7), 1851-1858, 2017 | 200 | 2017 |
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study E Mercuri, S Messina, C Bruno, M Mora, E Pegoraro, GP Comi, A D'Amico, ... Neurology 72 (21), 1802-1809, 2009 | 191 | 2009 |
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations P Melacini, M Fanin, DJ Duggan, MP Freda, A Berardinelli, GA Danieli, ... Muscle & Nerve: Official Journal of the American Association of …, 1999 | 176 | 1999 |
Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlation M Pane, ME Lombardo, P Alfieri, A D'Amico, F Bianco, G Vasco, G Piccini, ... The Journal of pediatrics 161 (4), 705-709. e1, 2012 | 172 | 2012 |
Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine E Mercuri, E Clements, A Offiah, A Pichiecchio, G Vasco, F Bianco, ... Annals of Neurology: Official Journal of the American Neurological …, 2010 | 163 | 2010 |
Phenotypic clustering of lamin A/C mutations in neuromuscular patients S Benedetti, I Menditto, M Degano, C Rodolico, L Merlini, A D’Amico, ... Neurology 69 (12), 1285-1292, 2007 | 163 | 2007 |
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Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA) E Fernandez-Vizarra, A Berardinelli, L Valente, V Tiranti, M Zeviani Journal of medical genetics 44 (3), 173-180, 2007 | 152 | 2007 |
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 | 144 | 2013 |
Antibodies to neurofascin, contactin-1, and contactin-associated protein 1 in CIDP: clinical relevance of IgG isotype A Cortese, R Lombardi, C Briani, I Callegari, L Benedetti, F Manganelli, ... Neurology: Neuroimmunology & Neuroinflammation 7 (1), e639, 2019 | 142 | 2019 |
Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36-month changes M Pane, ES Mazzone, S Sivo, MP Sormani, S Messina, A D′ Amico, ... PLoS One 9 (10), e108205, 2014 | 133 | 2014 |
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy M Ripolone, D Ronchi, R Violano, D Vallejo, G Fagiolari, E Barca, ... JAMA neurology 72 (6), 666-675, 2015 | 131 | 2015 |
Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy I Scionti, F Greco, G Ricci, M Govi, P Arashiro, L Vercelli, A Berardinelli, ... The American Journal of Human Genetics 90 (4), 628-635, 2012 | 124 | 2012 |