Long-term outcomes with agalsidase alfa enzyme replacement therapy : analysis using deconstructed composite events
dc.contributor.author | Beck, Michael | pt_BR |
dc.contributor.author | Hughes, Derralynn A. | pt_BR |
dc.contributor.author | Kampmann, Christoph | pt_BR |
dc.contributor.author | Pintos-Morell, G. | pt_BR |
dc.contributor.author | Ramaswami, Uma | pt_BR |
dc.contributor.author | West, Michael L. | pt_BR |
dc.contributor.author | Giugliani, Roberto | pt_BR |
dc.date.accessioned | 2019-06-22T02:35:01Z | pt_BR |
dc.date.issued | 2017 | pt_BR |
dc.identifier.issn | 2214-4269 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/10183/196083 | pt_BR |
dc.description.abstract | This is a retrospective analysis of Fabry Outcome Survey data from children/adults (n =677) receiving agalsidase alfa enzyme replacement therapy for a median of 3 years, examining cerebrovascular, cardiac, and renal morbidity endpoints separately. Cardiac events occurred at younger ages than cerebrovascular or renal events, cerebrovascular events were more frequent in females than males, and males were more likely to experience cardiac and renal events at a younger age than females. | en |
dc.format.mimetype | application/pdf | pt_BR |
dc.language.iso | eng | pt_BR |
dc.relation.ispartof | Molecular genetics and metabolism reports. Amsterdam. vol. 14 (Mar. 2018), p. 31-35 | pt_BR |
dc.rights | Open Access | en |
dc.subject | Terapia de reposição de enzimas | pt_BR |
dc.subject | Fabry disease | en |
dc.subject | Doença de Fabry | pt_BR |
dc.subject | Enzyme replacement therapy | en |
dc.subject | Agalsidase alfa | en |
dc.subject | Long-term effectiveness | en |
dc.title | Long-term outcomes with agalsidase alfa enzyme replacement therapy : analysis using deconstructed composite events | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dc.identifier.nrb | 001089836 | pt_BR |
dc.type.origin | Estrangeiro | pt_BR |
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