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hemophilia A
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factor VIII
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Bom, J.G. van der
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Desmopressin in nonsevere hemophilia A
Patients' and health care providers' perspectives on quality of hemophilia care in the Netherlands
A factor IX variant that functions independently of factor VIII mitigates the hemophilia
A factor IX variant that functions independently of factor VIII mitigates the hemophilia
Little discrepancy between one-stage and chromogenic factor VIII (FVIII)/IX assays in a large international cohort of persons with nonsevere hemophilia A and B
In patients with hemophilia, a decreased thrombin generation profile is associated with a severe bleeding phenotype
Time between inhibitor detection and start of immune tolerance induction: Association with outcome in the BrazIT study
Desmopressin for bleeding in non-severe hemophilia A
Socioeconomic participation of persons with hemophilia
Hepatitis C virus in hemophilia
Validation of PROMIS Profile-29 in adults with hemophilia in the Netherlands
Treatment-related risk factors for inhibitor development in non-severe hemophilia A after 50 cumulative exposure days
Patient-relevant health outcomes for hemophilia care
The factor VIII treatment history of non-severe hemophilia A
von Willebrand factor and factor VIII clearance in perioperative hemophilia a patients
Hemophilia management
Factor VIII products and inhibitor development in previously treated patients with severe or moderately severe hemophilia A: a systematic review
Prediction of factor VIII inhibitor development in the SIPPET cohort by mutational analysis and factor VIII antigen measurement
Timing and severity of inhibitor development in recombinant versus plasma-derived factor VIII concentrates: a SIPPET analysis
Intensity of factor VIII treatment and the development of inhibitors in non-severe hemophilia A patients: results of the INSIGHT case-control study
Mortality caused by intracranial bleeding in non-severe hemophilia A patients
Enhanced uptake of blood coagulation factor VIII containing immune complexes by antigen presenting cells
Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations
Perioperative treatment of hemophilia A patients: blood group O patients are at risk of bleeding complications
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