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Seminars in Thrombosis and Hemostasis|February 14, 2018
Inhibitors in Nonsevere Hemophilia A: What Is Known and Searching for the UnknownAmal Abdi, Silvia Linari, Lisa Pieri, et al.Pediatric Blood & Cancer|April 12, 2012
Micronutrients and sickle cell disease, effects on growth, infection and vaso-occlusive crisis: a systematic reviewLouise H Dekker, Karin Fijnvandraat, Bernard J Brabin, et al.Seminars in Thrombosis and Hemostasis|July 26, 2018
Preventing or Eradicating Factor VIII Antibody Formation in Patients with Hemophilia A: What Can We Learn from Other Disorders?Shermarke Hassan, Karin Fijnvandraat, Johanna G van der Bom, et al.Journal of Thrombosis and Haemostasis : JTH|January 12, 2025
Tolerance to factor VIII in the era of nonfactor therapies: immunologic perspectives and a systematic review of the literatureLilianne Esmée van Stam, Sébastien Lacroix-Desmazes, Karin Fijnvandraat, et al.Research and Practice in Thrombosis and Haemostasis|March 27, 2020
Hemophilia management: Huge impact of a tiny differenceFabienne Kloosterman, Anne-Fleur Zwagemaker, Amal Abdi, et al.British Journal of Haematology|May 20, 2014
Effect of von Willebrand factor on inhibitor eradication in patients with severe haemophilia A: a systematic reviewAlice S van Velzen, Marjolein Peters, Johanna G van der Bom, et al.Health and Quality of Life Outcomes|October 28, 2010
Double disadvantage: a case control study on health-related quality of life in children with sickle cell diseaseChanna T Hijmans, Karin Fijnvandraat, Jaap Oosterlaan, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|June 30, 2021
Adoption of emicizumab (Hemlibra®) for hemophilia A in Europe: Data from the 2020 European Association for Haemophilia and Allied Disorders surveyEvelien Krumb, Karin Fijnvandraat, Michael Makris, et al.Pediatric Blood & Cancer|June 15, 2011
Neurocognitive deficits in children with sickle cell disease are associated with the severity of anemiaChanna T Hijmans, Martha A Grootenhuis, Jaap Oosterlaan, et al.American Journal of Hematology|November 24, 2016
Daily pain in adults with sickle cell disease-a different perspectiveCharlotte F J van Tuijn, Joep W R Sins, Karin Fijnvandraat, et al.Pageof 16