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3. The Nijmegen ultra-sensitive Bethesda Assay detects very low-titer factor VIII inhibitors in patients with congenital and acquired hemophilia A

4. Anti-drug antibodies against the PEG moiety inhibit the procoagulant activity of therapeutic PEGylated FVIII

5. FVIII concentrate half-life heterogeneity in patients with haemophilia A is due to variability in endogenous VWF clearance.

7. Clinical use of thrombin generation assays

9. Recombinant ADAMTS13 reduces abnormally up-regulated von Willebrand factor in plasma from patients with severe COVID-19

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