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1. Variations in antenatal management and outcomes in haemolytic disease of the fetus and newborn: an international, retrospective, observational cohort study

2. Genetic variants, thrombocytopenia, and clinical phenotype of type 2B von Willebrand disease: a median 16-year follow-up study

5. Type 1 VWD classification revisited: novel insights from combined analysis of the LoVIC and WiN studies

9. Patients’ and health care providers’ perspectives on quality of hemophilia care in the Netherlands: a questionnaire and interview study

10. Colorectal cancer screening in patients with inherited bleeding disorders: high cancer detection rate in hemophilia patients

12. Postnatal treatment for children with fetal and neonatal alloimmune thrombocytopenia: a multicentre, retrospective, cohort study

13. Desmopressin response depends on the presence and type of genetic variants in patients with type 1 and type 2 von Willebrand disease

14. SYMPHONY consortium: Orchestrating personalized treatment for patients with bleeding disorders

16. Patient‐reported data on the severity of Von Willebrand disease.

18. Efficacy and Safety Analyses of Recombinant Factor VIIa in Severe Post-Partum Hemorrhage

20. Hepatitis C virus in hemophilia: Health‐related quality of life after successful treatment in the sixth Hemophilia in the Netherlands study

21. Treatment‐related risk factors for inhibitor development in non‐severe hemophilia A after 50 cumulative exposure days: A case‐control study

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

23. Patient‐relevant health outcomes for hemophilia care: Development of an international standard outcomes set

25. Mortality, life expectancy, and causes of death of persons with hemophilia in the Netherlands 2001–2018

28. The factor VIII treatment history of non‐severe hemophilia A

29. ADAMTS‐13 and bleeding phenotype in von Willebrand disease

31. Laboratory approach for vaccine‐induced thrombotic thrombocytopenia diagnosis in the Netherlands

32. Challenging the dogma: Red blood cell‐directed autoimmunity as risk factor for red blood cell alloimmunisation after blood transfusion

34. Type 1 VWD classification revisited - novel insights from combined analysis of the LoVIC and WiN studies

35. Challenging the dogma: Red blood cell-directed autoimmunity as risk factor for red blood cell alloimmunisation after blood transfusion

36. Transfusion of ever-pregnant donor red blood cells and mortality of male patients

37. The spectrum of neutralizing and non-neutralizing anti-FVIII antibodies in a nationwide cohort of 788 persons with hemophilia A

38. Description of mitochondrial oxygen tension and its variability in healthy volunteers

39. Donor pregnancies and transfusion recipient mortality: A role for red blood cell storage?

44. Type 1 VWD classification revisited - novel insights from combined analysis of the LoVIC and WiN studies

47. Hemostatic efficacy of pathogen-inactivated vs untreated platelets: a randomized controlled trial

48. Transition readiness among adolescents and young adults with haemophilia in the Netherlands: Nationwide questionnaire study

49. The spectrum of neutralizing and non-neutralizing anti-FVIII antibodies in a nationwide cohort of 788 persons with hemophilia A.

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