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1. A Blended Physiotherapy Intervention for Persons With Hemophilic Arthropathy: Development Study

2. A bispecific antibody approach for the potential prophylactic treatment of inherited bleeding disorders

3. Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database

6. Efficacy of a 1:1 ratio VWF/FVIII concentrate in patients with von Willebrand disease.

8. Apixaban versus no anticoagulation after anticoagulation-associated intracerebral haemorrhage in patients with atrial fibrillation in the Netherlands (APACHE-AF): a randomised, open-label, phase 2 trial

9. Perioperative pharmacokinetic-guided factor VIII concentrate dosing in haemophilia (OPTI-CLOT trial): an open-label, multicentre, randomised, controlled trial

11. Limited value of testing for factor XIII and α2‐antiplasmin deficiency in patients with a bleeding disorder of unknown cause.

12. Metabolic blood profile and response to treatment with the pyruvate kinase activator mitapivat in patients with sickle cell disease.

13. Towards Personalized Treatment in Haemophilia: The Role of Genetic Factors in Iron and Heme Control to Identify Patients at Risk for Haemophilic Arthropathy.

14. Subclinical synovial proliferation in patients with severe haemophilia A: The value of ultrasound screening and biochemical markers

16. Clotting factor activity levels and bleeding risk in people with haemophilia playing sports

17. Structural changes after ankle joint distraction in haemophilic arthropathy: an explorative study investigating biochemical markers and 3D joint space width

19. The efficacy of the entire-vial dosing of emicizumab: Real-world evidence on plasma concentrations, bleeds, and drug waste

20. One-year safety and efficacy of mitapivat in sickle cell disease: follow-up results of a phase 2, open-label study

21. Toward responsible clinical n-of-1 strategies for rare diseases

22. No immunological changes after factor VIII product switch: An in depth analysis in haemophilia A patients

23. Structural changes after ankle joint distraction in haemophilic arthropathy: an explorative study investigating biochemical markers and 3D joint space width

24. Functional decline in persons with haemophilia and factors associated with deterioration

25. Blood coagulation and beyond: Position paper from the Fourth Maastricht Consensus Conference on Thrombosis

26. Magnetic resonance imaging evidence for subclinical joint bleeding in a Dutch population of people with severe hemophilia on prophylaxis

27. MarioHeart: Novel In-Vitro Flow Model for Testing Heart Valve Prostheses and Anticoagulant Therapies

28. Proof of concept and feasibility of a blended physiotherapy intervention for persons with haemophilic arthropathy

31. Lupus anticoagulant associates with thrombosis in patients with COVID-19 admitted to intensive care units

34. Ankle joint distraction is a promising alternative treatment for patients with severe haemophilic ankle arthropathy

37. Enhanced hepatic clearance of hyposialylated platelets explains thrombocytopenia in GNE-related macrothrombocytopenia

40. Design of a Prospective Study on Pharmacokinetic-Guided Dosing of Prophylactic Factor Replacement in Hemophilia A and B (OPTI-CLOT TARGET Study)

41. Lupus anticoagulant associates with thrombosis in patients with COVID-19 admitted to intensive care units:A retrospective cohort study

42. Design of a Prospective Study on Pharmacokinetic-Guided Dosing of Prophylactic Factor Replacement in Hemophilia A and B (OPTI-CLOT TARGET Study)

43. Gene Therapy for Hemophilia A: How Long Will It Last?

44. Menstrual problems in chronic immune thrombocytopenia: A monthly challenge - a cohort study and review

45. Safety and efficacy of mitapivat, an oral pyruvate kinase activator, in sickle cell disease: a phase 2, open-label study

46. Predicting Individual Changes in Terminal Half-Life After Switching to Extended Half-Life Concentrates in Patients With Severe Hemophilia

47. Reduced cardiovascular morbidity in patients with hemophilia: results of a 5-year multinational prospective study

48. Relapse of immune thrombocytopenia after COVID-19 vaccination

49. Prevalence, burden and treatment effects of vaginal bleeding in women with (suspected) congenital platelet disorders throughout life: a cross-sectional study

50. Emicizumab Dosing in Children and Adults with Hemophilia A: Simulating a User-Friendly and Cost-Efficient Regimen

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