CAO, MICHELANGELO
CAO, MICHELANGELO
Università di Padova
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations
2016 Cao, Michelangelo; Dona', Marta; Valentino, Lucia; Semplicini, Claudio; Maresca, Alessandra; Cassina, Matteo; Torraco, Alessandra; Galletta, Eva; Manfioli, Valeria; Soraru', Gianni; Carelli, Valerio; Stramare, Roberto; Bertini, Enrico; Carozzo, Rosalba; Salviati, Leonardo; Pegoraro, Elena
Facio-scapulo-humeral dystrophy: clinical follow-up and role of chromosome X inactivation in female patients - SHP2: a novel therapeutic target in MuSK-myasthenia
2018 Cao, Michelangelo
FSHD1 and FSHD2 form a disease continuum
2019 Sacconi, Sabrina; Briand-Suleau, Audrey; Gros, Marilyn; Baudoin, Christian; Lemmers, Richard J L F; Rondeau, Sophie; Lagha, Nadira; Nigumann, Pilvi; Cambieri, Chiara; Puma, Angela; Chapon, Françoise; Stojkovic, Tanya; Vial, Christophe; Bouhour, Françoise; Cao, Michelangelo; Pegoraro, Elena; Petiot, Philippe; Behin, Anthony; Marc, Bras; Eymard, Bruno; Echaniz-Laguna, Andoni; Laforet, Pascal; Salviati, Leonardo; Jeanpierre, Marc; Cristofari, Gaël; van der Maarel, Silvère M
No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype
2016 Bertolin, Cinzia; Querin, Giorgia; Da Re, E.; Sagnelli, A.; Bello, Luca; Cao, Michelangelo; Muscas, M.; Pennuto, M.; Ermani, Mario; Pegoraro, Elena; Mariotti, C.; Gellera, C.; Hanna, M. G.; Pareyson, D.; Fratta, P.; Soraru', Gianni; Pennuto, Maria