Browsing by Subject Muscles -- Diseases
Showing results 1 to 4 of 4
Issue Date | Title | Author(s) |
2016 | A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release | D'Adamo, Maria Cristina; Sforna, Luigi; Visentin, Sergio; Grottesi, Alessandro; Servettini, Ilenio; Guglielmi, Luca; Macchioni, Lara; Saredi, Simona; Curcio, Maurizio; Nuccio, Chiara de; Hasan, Sonia M.; Corazzi, L.; Franciolini, Fabio; Mora, Marina; Catacuzzeno, Luigi; Pessia, Mauro |
2009 | Is general practice the optimal setting for the recognition of statin-induced myotoxicity? | Sciberras, David; Robinson, Victor; Calleja, Neville |
2019-03 | Pharmacogenetic testing for personalisation of statin therapy | Cerdá Iñesta, Judith; Wirth, Francesca; Mifsud Buhagiar, Luana; Zahra, Graziella; Xuereb, Robert G.; Barbara, Christopher; Serracino-Inglott, Anthony |
2018-09 | SLCO1B1 genetic polymorphisms in cardiac patients on simvastatin | Cerdá Iñesta, Judith; Wirth, Francesca; Zahra, Graziella; Xuereb, Robert G.; Barbara, Christopher; Serracino-Inglott, Anthony |