Zobrazeno 1 - 10 of 173 pro vyhledávání: '"D'Angelo, MG"'
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Akademický článek
Assessment and management of respiratory function in patients with Duchenne muscular dystrophy: current and emerging options
Autor: LoMauro A, D’Angelo MG, Aliverti A
Publikováno v: Therapeutics and Clinical Risk Management, Vol 2015, Iss default, Pp 1475-1488 (2015)
Antonella LoMauro,1 Maria Grazia D’Angelo,2 Andrea Aliverti1 1Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, 2IRCCS Eugenio Medea, Bosisio Parini, Italy Abstract: Duchenne muscular dystrophy (DMD) is an X-l
Externí odkaz: https://doaj.org/article/9d9a6642af994ff4baa795c4ea82f79c
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2
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase
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
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3
Efficacy of idebenone on respiratory function in patients with Duchenne muscular dystrophy not using glucocorticoids (DELOS): a double-blind randomised placebo-controlled phase 3 trial
Autor: Buyse GM, Voit T, Schara U, Straathof CS, D'Angelo MG, Bernert G, Cuisset JM, Finkel RS, Goemans N, McDonald CM, Rummey C, Meier T, DELOS Study Group, POLITANO, Luisa
Publikováno v: Lancet, 385(9979), 1748-1757
SummaryBackgroundCardiorespiratory failure is the leading cause of death in Duchenne muscular dystrophy. Based on preclinical and phase 2 evidence, we assessed the efficacy and safety of idebenone in young patients with Duchenne muscular dystrophy wh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc0ab1c2b9f7f7345e6b42729886c820
https://doi.org/10.1016/s0140-6736(15)60025-3
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6
Infantile-onset Hereditary spastic paraplegia associated with SPAST mutations (SPG4): clinical and follow-up studies
Autor: Casali C, Piccolo F, Marcotulli C, Santorelli F, Tessa A, Di Fabio R, D’Angelo MG, Serrao M, Pierelli F, MELONE, Mariarosa Anna Beatrice
Introduction: Hereditary spastic paraplegia (HSP) associated with SPAST mutations (SPG4) is the most frequent form of autosomal dominant HSP accounting approximately for 40% of reported cases. The phenotype associated with HSP due to mutation in the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3977::fef28bb14990d7fae089d1f1d8f63d01
http://hdl.handle.net/11591/222742
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