Luca Bello
Luca Bello
Department of Neurosciences DNS, University of Padova
Email verificata su
Citata da
Citata da
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E
C Semplicini, J Vissing, JR Dahlqvist, T Stojkovic, L Bello, N Witting, ...
Neurology 84 (17), 1772-1781, 2015
A Mutation in the CASQ1 Gene Causes a Vacuolar Myopathy with Accumulation of Sarcoplasmic Reticulum Protein Aggregates
D Rossi, B Vezzani, L Galli, C Paolini, L Toniolo, E Pierantozzi, S Spinozzi, ...
Human mutation 35 (10), 1163-1170, 2014
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
Articoli 1–20