BELLO, LUCA
BELLO, LUCA
Dipartimento di Neuroscienze - DNS
226thENMC International Workshop:. Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20-22 January 2017, Heemskerk, The Netherlands
2017 Aartsma-Rus, Annemieke; Ferlini, Alessandra; Mcnally, Elizabeth M.; Spitali, Pietro; Sweeney, H. Lee; Al-Khalili Szigyarto, Christina; Bello, Luca; Bronson, Abby; Brown, Kristy; Buccella, Filippo; Chadwick, Jessica; Frank, Diane; Hoffman, Eric; Larkindale, Jane; Mcclorey, G.; Munschauer, Rick; Muntoni, Francesco; Owens, Jane; Schara, Ulrike; Spitali, Pietro; Straub, Volker; Tinsley, Jon; Versnel, Jenny; Vroom, Elizabeth; Welch, Ellen
24 month longitudinal data in ambulant boys with duchenne muscular dystrophy.
2013 Mazzone, Es; Pane, M; Sormani, Mp; Scalise, R; Berardinelli, A; Messina, S; Torrente, Y; D'Amico, A; Doglio, L; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, Luca; Bonfiglio, S; De Sanctis, R; Rolle, E; Bianco, F; Magri, F; Rossi, F; Vasco, G; Vita, G; Motta, Mc; Donati, Ma; Sacchini, M; Mongini, T; Pini, A; Battini, R; Pegoraro, Elena; Previtali, S; Napolitano, S; Bruno, C; Politano, L; Comi, Gp; Bertini, E; Mercuri, E.
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes.
2014 Pane, M; Mazzone, Es; Sormani, Mp; Messina, S; Vita, Gl; Fanelli, L; Berardinelli, A; Torrente, Y; D'Amico, A; Lanzillotta, V; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, Luca; Bonfiglio, S; Scalise, R; De Sanctis, R; Rolle, E; Bianco, F; Van der Haawue, M; Magri, F; Palermo, C; Rossi, F; Donati, Ma; Alfonsi, C; Sacchini, M; Arnoldi, Mt; Baranello, G; Mongini, T; Pini, A; Battini, R; Pegoraro, Elena; Previtali, Sc; Napolitano, S; Bruno, C; Politano, L; Comi, Gp; Bertini, E; Morandi, L; Gualandi, F; Ferlini, A; Goemans, N; Mercuri, E.
A Mutation in the CASQ1 Gene Causes a Vacuolar Myopathy with Accumulation of Sarcoplasmic Reticulum Protein Aggregates.
2014 Rossi, D; Vezzani, B; Galli, L; Paolini, C; Toniolo, Luana; Pierantozzi, E; Spinozzi, S; Barone, V; Pegoraro, Elena; Bello, Luca; Cenacchi, G; Vattemi, G; Tomelleri, G; Ricci, G; Siciliano, G; Protasi, F; Reggiani, Carlo; Sorrentino, V.
Ablation of collagen VI leads to the release of platelets with altered function
2021 Abbonante, V.; Gruppi, C.; Battiston, M.; Zulian, A.; Di Buduo, C. A.; Chrisam, M.; Sereni, L.; Laurent, P. -A.; Semplicini, C.; Lombardi, E.; Mazzucato, M.; Moccia, F.; Petronilli, V.; Villa, A.; Bello, L.; Pegoraro, E.; Bernardi, P.; Braghetta, P.; De Marco, L.; Bonaldo, P.; Balduini, A.
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy
2022 Coratti, Giorgia; Lenkowicz, Jacopo; Norcia, Giulia; Lucibello, Simona; Ferraroli, Elisabetta; D'Amico, Adele; Bello, Luca; Pegoraro, Elena; Messina, Sonia; Ricci, Federica; Mongini, Tiziana; Berardinelli, Angela; Masson, Riccardo; Previtali, Stefano C; D'Angelo, Grazia; Magri, Francesca; Comi, Giacomo P; Politano, Luisa; Passamano, Luigia; Vita, Gianluca; Sansone, Valeria A; Albamonte, Emilio; Panicucci, Chiara; Bruno, Claudio; Pini, Antonella; Bertini, Enrico; Patarnello, Stefano; Pane, Marika; Mercuri, Eugenio
Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale
2021 Jacobs, M. B.; James, M. K.; Lowes, L. P.; Alfano, L. N.; Eagle, M.; Muni Lofra, R.; Moore, U.; Feng, J.; Rufibach, L. E.; Rose, K.; Duong, T.; Bello, L.; Pedrosa-Hernandez, I.; Holsten, S.; Sakamoto, C.; Canal, A.; Sanchez-Aguilera Praxedes, N.; Thiele, S.; Siener, C.; Vandevelde, B.; Dewolf, B.; Maron, E.; Guglieri, M.; Hogrel, J. -Y.; Blamire, A. M.; Carlier, P. G.; Spuler, S.; Day, J. W.; Jones, K. J.; Bharucha-Goebel, D. X.; Salort-Campana, E.; Pestronk, A.; Walter, M. C.; Paradas, C.; Stojkovic, T.; Mori-Yoshimura, M.; Bravver, E.; Diaz-Manera, J.; Pegoraro, E.; Mendell, J. R.; Mayhew, A. G.; Straub, V.
Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach
2022 Mayhew, A. G.; James, M. K.; Moore, U.; Sutherland, H.; Jacobs, M.; Feng, J.; Lowes, L. P.; Alfano, L. N.; Muni Lofra, R.; Rufibach, L. E.; Rose, K.; Duong, T.; Bello, L.; Pedrosa-Hernandez, I.; Holsten, S.; Sakamoto, C.; Canal, A.; Sanchez-Aguilera Praxedes, N.; Thiele, S.; Siener, C.; Vandevelde, B.; Dewolf, B.; Maron, E.; Gordish-Dressman, H.; Hilsden, H.; Guglieri, M.; Hogrel, J. -Y.; Blamire, A. M.; Carlier, P. G.; Spuler, S.; Day, J. W.; Jones, K. J.; Bharucha-Goebel, D. X.; Salort-Campana, E.; Pestronk, A.; Walter, M. C.; Paradas, C.; Stojkovic, T.; Mori-Yoshimura, M.; Bravver, E.; Diaz-Manera, J.; Pegoraro, E.; Mendell, J. R.; Jain COS, Consortium; Straub, V.
Assessment of disease progression in dysferlinopathy: A 1-year cohort study
2019 Moore, U.; Jacobs, M.; James, M. K.; Mayhew, A. G.; Fernandez-Torron, R.; Feng, J.; Cnaan, A.; Eagle, M.; Bettinson, K.; Rufibach, L. E.; Lofra, R. M.; Blamire, A. M.; Carlier, P. G.; Mittal, P.; Lowes, L. P.; Alfano, L.; Rose, K.; Duong, T.; Berry, K. M.; Montiel-Morillo, E.; Pedrosa-Hernandez, I.; Holsten, S.; Sanjak, M.; Ashida, A.; Sakamoto, C.; Tateishi, T.; Yajima, H.; Canal, A.; Ollivier, G.; Decostre, V.; Mendez, J. B.; Praxedes, N. S. -A.; Thiele, S.; Siener, C.; Shierbecker, J.; Florence, J. M.; Vandevelde, B.; Dewolf, B.; Hutchence, M.; Gee, R.; Prugel, J.; Maron, E.; Hilsden, H.; Lochmuller, H.; Grieben, U.; Spuler, S.; Rocha, C. T.; Day, J. W.; Jones, K. J.; Bharucha-Goebel, D. X.; Salort-Campana, E.; Harms, M.; Pestronk, A.; Krause, S.; Schreiber-Katz, O.; Walter, M. C.; Paradas, C.; Hogrel, J. -Y.; Stojkovic, T.; Takeda, S.; Mori-Yoshimura, M.; Bravver, E.; Sparks, S.; Diaz-Manera, J.; Bello, L.; Semplicini, C.; Pegoraro, E.; Mendell, J. R.; Bushby, K.; Straub, V.
Assessment of patients with idiopathic inflammatory myopathies and isolated creatin-kinase elevation
2014 Iaccarino, Luca; Pegoraro, Elena; Bello, Luca; S., Bettio; E., Borella; L., Nalotto; Semplicini, Claudio; Soraru', Gianni; Ghirardello, Anna; Doria, Andrea
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy
2016 Bello, Luca; Flanigan, Kevin M; Weiss, Robert B; Spitali, Pietro; Aartsma Rus, Annemieke; Muntoni, Francesco; Zaharieva, Irina; Ferlini, Alessandra; Mercuri, Eugenio; Tuffery Giraud, Sylvie; Claustres, Mireille; Straub, Volker; Lochmüller, Hanns; Barp, Andrea; Vianello, Sara; Pegoraro, Elena; Punetha, Jaya; Gordish Dressman, Heather; Giri, Mamta; Mcdonald, Craig M; Hoffman, Eric P.
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript
2016 Todeschini, Alice; Gualandi, Francesca; Trabanelli, Cecilia; Armaroli, Annarita; Ravani, Anna; Fanin, Marina; Rota, Silvia; Bello, Luca; Ferlini, Alessandra; Pegoraro, Elena; Padovani, Alessandro; Filosto, Massimiliano
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test
2015 Pane, Marika; Fanelli, Lavinia; Mazzone, Elena Stacy; Olivieri, Giorgia; D'Amico, Adele; Messina, Sonia; Scutifero, Marianna; Battini, Roberta; Petillo, Roberta; Frosini, Silvia; Sivo, Serena; Vita, Gian Luca; Bruno, Claudio; Mongini, Tiziana; Pegoraro, Elena; De Sanctis, Roberto; Gardani, Alice; Berardinelli, Angela; Lanzillotta, Valentina; Carlesi, Adelina; Viggiano, Emanuela; Cavallaro, Filippo; Sframeli, Maria; Bello, Luca; Barp, Andrea; Bianco, Flaviana; Bonfiglio, Serena; Rolle, Enrica; Palermo, Concetta; D'Angelo, Grazia; Pini, Antonella; Iotti, Elena; Gorni, Ksenija; Baranello, Giovanni; Bertini, Enrico; Politano, Luisa; Sormani, Maria Pia; Mercuri, Eugenio
Burden, professional support, and social network in families of children and young adults with muscular dystrophies
2014 L., Magliano; M., Patalano; A., Sagliocchi; M., Scutifero; A., Zaccaro; M. G., D'Angelo; F., Civati; E., Brighina; G., Vita; G. L., Vita; Messina, S; Sframeli, M; Pane, M; Lombardo, Me; Scalise, R; D'Amico, A; Colia, G; Catteruccia, M; Balottin, U; Berardinelli, A; Motta, Mc; Angelini, Corrado; Gaiani, Alessandra; Semplicini, Claudio; Bello, Luca; Battini, R; Astrea, G; Politano, L.
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy.
2012 Bello, Luca; Melacini, P; Pezzani, R; D'Amico, A; Piva, L; Leonardi, E; Torella, A; Soraru', Gianni; Palmieri, Arianna; Smaniotto, G; Gavassini, Bf; Vianello, A; Nigro, V; Bertini, E; Angelini, C; Tosatto, Silvio; Pegoraro, Elena
Cardiorespiratory management of Duchenne muscular dystrophy: emerging therapies, neuromuscular genetics, and new clinical challenges
2022 Birnkrant, D. J.; Bello, L.; Butterfield, R. J.; Carter, J. C.; Cripe, L. H.; Cripe, T. P.; Mckim, D. A.; Nandi, D.; Pegoraro, E.
Caregiver psychological profile and perceived quality of life in children affected by Duchenne Muscular Dystrophy
2013 Barp, Andrea; Marcato, Sonia; Palmieri, Arianna; Calvo, Vincenzo; Kleinbub, JOHANN ROLAND; Bello, Luca; Pegoraro, Elena
Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular Dystrophy
2017 Nghiem, Peter P; Bello, Luca; Stoughton, William B; López, Sara Mata; Vidal, Alexander H; Hernandez, Briana V; Hulbert, Katherine N; Gourley, Taylor R; Bettis, Amanda K; Balog-Alvarez, Cynthia J; Heath-Barnett, Heather; Kornegay, Joe N
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E
2015 Semplicini, Claudio; Vissing, John; Dahlqvist, Julia R.; Stojkovic, Tanya; Bello, Luca; Witting, Nanna; Duno, Morten; Leturcq, France; Bertolin, Cinzia; D'Ambrosio, Paola; Eymard, Bruno; Angelini, Corrado; Politano, Luisa; Laforêt, Pascal; Pegoraro, Elena
Clinical and molecular characterization of limb girdle muscular dystrophy due to LAMA2 mutations.
2011 Gavassini, Bf; Carboni, N; Nielsen, Je; Danielsen, Er; Thomsen, C; Svenstrup, K; Bello, Luca; Maioli, Ma; Marrosu, G; Ticca, Af; Mura, M; Marrosu, Mg; Soraru', Gianni; Angelini, C; Vissing, J; Pegoraro, Elena