Sfoglia per Autore
Severe cardiomyopathy in a young patient with complete deficiency of adipose triglyceride lipase due to a novel mutation in PNPLA2 gene
2016 M.B. Pasanisi, S. Missaglia, D. Cassandrini, F. Salerno, S. Farina, D. Andreini, P. Agostoni, L. Morandi, M. Mora, D. Tavian
Interpreting Genetic Variants in Titin in Patients With Muscle Disorders
2018 M. Savarese, L. Maggi, A. Vihola, P.H. Jonson, G. Tasca, L. Ruggiero, L. Bello, F. Magri, T. Giugliano, A. Torella, A. Evila, G. Di Fruscio, O. Vanakker, S. Gibertini, L. Vercelli, A. Ruggieri, C. Antozzi, H. Luque, S. Janssens, M.B. Pasanisi, C. Fiorillo, M. Raimondi, M. Ergoli, L. Politano, C. Bruno, A. Rubegni, M. Pane, F.M. Santorelli, C. Minetti, C. Angelini, J. De Bleecker, M. Moggio, T. Mongini, G.P. Comi, L. Santoro, E. Mercuri, E. Pegoraro, M. Mora, P. Hackman, B. Udd, V. Nigro
Exercise training alone or in combination with high-protein diet in patients with late onset Pompe disease : Results of a cross over study
2020 A. Sechi, L. Zuccarelli, B. Grassi, R. Frangiamore, R. De Amicis, M. Marzorati, S. Porcelli, A. Tullio, A. Bacco, S. Bertoli, A. Dardis, L. Biasutti, M.B. Pasanisi, G. Devigili, B. Bembi
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| Severe cardiomyopathy in a young patient with complete deficiency of adipose triglyceride lipase due to a novel mutation in PNPLA2 gene | 2016 | M.B. PasanisiS. FarinaD. AndreiniP. Agostoni + | Article (author) | - | |
| Interpreting Genetic Variants in Titin in Patients With Muscle Disorders | 2018 | F. MagriM. B. PasanisiG. P. Comi + | Article (author) | - | |
| Exercise training alone or in combination with high-protein diet in patients with late onset Pompe disease : Results of a cross over study | 2020 | Grassi B.Frangiamore R.De Amicis R.Porcelli S.Bertoli S.Pasanisi M. B. + | Article (author) | - |
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