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- W2398829893 endingPage "1516" @default.
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- W2398829893 abstract "Mild inherited bleeding disorders are relatively common in the general population. Despite recent advances in diagnostic approaches, mild inherited bleeding disorders still pose a significant diagnostic challenge. Hemorrhagic diathesis can be caused by disorders in primary hemostasis (von Willebrand disease, inherited platelet function disorders), secondary hemostasis (hemophilia A and B, other (rare) coagulant factor deficiencies) and fibrinolysis, and in connective tissue or vascular formation. This review summarizes the currently available diagnostic methods for mild bleeding disorders and their pitfalls, from structured patient history to highly specialized laboratory diagnosis. A comprehensive framework for a diagnostic approach to mild inherited bleeding disorders is proposed." @default.
- W2398829893 created "2016-06-24" @default.
- W2398829893 creator A5002870795 @default.
- W2398829893 creator A5019591784 @default.
- W2398829893 creator A5090296015 @default.
- W2398829893 date "2016-08-01" @default.
- W2398829893 modified "2023-10-16" @default.
- W2398829893 title "A diagnostic approach to mild bleeding disorders" @default.
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- W2398829893 doi "https://doi.org/10.1111/jth.13368" @default.
- W2398829893 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27208505" @default.
- W2398829893 hasPublicationYear "2016" @default.
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