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Cerebrovascular Diseases (Basel, Switzerland)|March 14, 2015
Cerebral lesions on 7 tesla MRI in patients with sickle cell anemiaVeronica van der Land, Jaco J M Zwanenburg, Karin Fijnvandraat, et al.Journal of Thrombosis and Haemostasis : JTH|February 16, 2022
Joint status of patients with nonsevere hemophilia AAnne-Fleur Zwagemaker, Fabienne R Kloosterman, Robert Hemke, et al.Journal of Thrombosis and Haemostasis : JTH|February 5, 2026
The MAPTO survey: Worldwide Approaches on Unmasking Factor VIII Inhibitors in Children with Emicizumab Treatment: Communication from the ISTH SSC Subcommittee on Factor VIII, Factor IX and Rare Coagulation DisordersLilianne Esmée van Stam, Bridget Jane Daisy Horstman, Pantep Angchaisuksiri, et al.Haematologica|March 2, 2019
Dynamic prediction of bleeding risk in thrombocytopenic preterm neonatesSusanna F Fustolo-Gunnink, Karin Fijnvandraat, Hein Putter, et al.Stroke|January 20, 2009
Cerebral blood flow measurement in children with sickle cell disease using continuous arterial spin labeling at 3.0-Tesla MRIXandra W van den Tweel, Aart J Nederveen, Charles B L M Majoie, et al.Nederlands Tijdschrift Voor Geneeskunde|May 8, 2014
[Von Willebrand disease in the Netherlands: the WiN study]Yvonne V Sanders, Eva M de Wee, Karina Meijer, et al.American Journal of Hematology|September 17, 2015
Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric-specific bleedingYvonne V Sanders, Karin Fijnvandraat, Johan Boender, et al.British Journal of Haematology|October 23, 2015
Risk factor analysis of cerebral white matter hyperintensities in children with sickle cell diseaseVeronica van der Land, Henri J M M Mutsaerts, Marc Engelen, et al.Thrombosis and Haemostasis|January 6, 2018
Circulating Angiogenic Mediators in Patients with Moderate and Severe von Willebrand Disease: A Multicentre Cross-Sectional StudyDafna J Groeneveld, Yvonne V Sanders, Jelle Adelmeijer, et al.Journal of Thrombosis and Haemostasis : JTH|July 23, 2024
International Society on Thrombosis and Haemostasis clinical practice guideline for treatment of congenital hemophilia A and B based on the Grading of Recommendations Assessment, Development, and Evaluation methodologySuely M Rezende, Ignacio Neumann, Pantep Angchaisuksiri, et al.Pageof 16