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- W2318065996 abstract "Von Willebrand disease (vWD) is the most common inherited bleeding disorder which results from quantitative or qualitative defect of plasma glycoprotein, von Willebrand factor (vWF). The diagnosis is diffi cult and multistep because of its clinical and molecular heterogeneity. The interpretation of laboratory results, especially in type 1 vWD, may be challenging due to pathophysiological variability of vWF." @default.
- W2318065996 created "2016-06-24" @default.
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- W2318065996 date "2013-01-01" @default.
- W2318065996 modified "2023-09-23" @default.
- W2318065996 title "Klasyfi kacja i diagnostyka choroby von Willebranda Classifi cation and diagnosis of von Willebrand disease" @default.
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