Zobrazeno 1 - 10
of 855
pro vyhledávání: '"Santorelli, Fm."'
Autor:
Mauri, E, Abati, E, Musumeci, O, Rodolico, C, D'Angelo, Mg, Mirabella, M, Lucchini, M, Bello, L, Pegoraro, E, Maggi, L, Manneschi, L, Gemelli, C, Grandis, M, Zuppa, A, Massucco, S, Benedetti, L, Caponnetto, C, Schenone, A, Prelle, A, Previtali, Sc, Scarlato, M, D'Amico, A, Bertini, E, Pennisi, Em, De Giglio, L, Pane, M, Mercuri, E, Mongini, T, Ricci, F, Berardinelli, A, Astrea, G, Lenzi, S, Battini, R, Ricci, G, Torri, F, Siciliano, G, Santorelli, Fm, Ariatti, A, Filosto, M, Passamano, L, Politano, L, Scutifero, M, Tonin, P, Fossati, B, Panicucci, C, Bruno, C, Ravaglia, S, Monforte, M, Tasca, G, Ricci, E, Petrucci, A, Santoro, L, Ruggiero, L, Barp, A, Albamonte, E, Sansone, V, Gagliardi, D, Costamagna, G, Govoni, A, Magri, F, Brusa, R, Velardo, D, Meneri, M, Sciacco, M, Corti, S, Bresolin, N, Moroni, I, Messina, S, Di Muzio, A, Nigro, V, Liguori, R, Antonini, G, Toscano, A, Minetti, C, Comi, Gp, Italian Association of, Myology.
Publikováno v:
Acta Myologica
Introduction. Since February 2020, the outbreak of COVID-19 in Italy has forced the health care system to undergo profound rearrangements in its services and facilities, especially in the worst-hit areas in Northern Italy. In this setting, inpatient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3e93c196887c46b4509bfc054f8059d7
http://hdl.handle.net/11562/1024694
http://hdl.handle.net/11562/1024694
Autor:
Astrea G, Pecini C, Gasperini F, Brisca G, Scutifero M, Bruno C, Santorelli FM, Cioni G, Chilosi AM, Battini R., POLITANO, Luisa
Below-average reading performances have been reported in individuals with Duchenne muscular dystrophy (DMD), but literacy problems in these subjects have yet to be characterized. In this study, the presence and characteristics of literacy deficits in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::c4df20d45600f1dd58a0a0b2f15eb676
http://hdl.handle.net/11591/181740
http://hdl.handle.net/11591/181740
The dystroglycanopathies, which are caused by reduced glycosylation of alpha-dystroglycan, are a heterogeneous group of neurodegenerative disorders characterized by variable brain and skeletal muscle involvement. Recently, mutations in TMEM5 have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::10a2516bac6a897c50b41d42937f96d2
http://hdl.handle.net/11591/368479
http://hdl.handle.net/11591/368479
Autor:
Mancuso, M, Orsucci, D, Angelini, C, Bertini, E, Catteruccia, M, Pegoraro, E, Carelli, V, Valentino, Ml, Comi, Gp, Minetti, C, Bruno, C, Moggio, M, Ienco, Ec, Mongini, T, Vercelli, L, Primiano, Guido Alessandro, Servidei, Serenella, Tonin, P, Scarpelli, M, Toscano, A, Musumeci, O, Moroni, I, Uziel, G, Santorelli, Fm, Nesti, C, Filosto, M, Lamperti, C, Zeviani, M, Siciliano, G.
Myoclonus is a possible manifestation of mitochondrial disorders, and its presence is considered, in association with epilepsy and the ragged red fibers, pivotal for the syndromic diagnosis of MERRF (myoclonic epilepsy with ragged red fibers). Howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0f114a996606433a37f54d784a13fae8
http://hdl.handle.net/11577/2806259
http://hdl.handle.net/11577/2806259
Autor:
Fiorillo, C, Moro, F, Yi, J, Weil, S, Brisca, G, Astrea, G, Severino, M, Romano, A, Battini, R, Rossi, A, Minetti, C, Bruno, C, Santorelli, Fm, Vallee, R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7284dd019bc52ccfc23a2aeb2b74cb8a
http://hdl.handle.net/11567/820420
http://hdl.handle.net/11567/820420