Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/10727
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dc.contributor.authorA. Klukowskaen_US
dc.contributor.authorA. Skotnickien_US
dc.contributor.authorT. Lissitchkoven_US
dc.contributor.authorV. Mamonoven_US
dc.contributor.authorE. Buevichen_US
dc.contributor.authorK. Kuliczkowskien_US
dc.contributor.authorS. Goranoven_US
dc.contributor.authorJ. Kolczkoen_US
dc.contributor.authorS. Stankovicen_US
dc.contributor.authorW. Seiferten_US
dc.date.accessioned2021-03-08T18:38:41Z-
dc.date.available2021-03-08T18:38:41Z-
dc.date.issued2014-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/10727-
dc.language.isoenen_US
dc.relation.ispartofHaemophiliaen_US
dc.subjecthemophilia Aen_US
dc.subjectplasma-derived concentrateen_US
dc.subjectSWIFT-HA studyen_US
dc.titleEfficasy, safety, and pharmacokinetics results of a phase II/III, multicentre, double-blinded, randomized, cross-over study with a plasma-derived von Wilebrand Factor (WVF)/factor VIII (FVIII) concentrate (Voncento) in subjects with hemophilia A (the SWIFT-HA Study)en_US
dc.typeProceeding articleen_US
dc.relation.conferenceWorld Federation of Hemophilia (WFH) World Congress 2014, Melbourne, Australiaen_US
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Conference papers
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