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British Journal of Haematology|May 17, 2018
Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand diseaseFerdows Atiq, Karina Meijer, Jeroen Eikenboom, et al.
British Journal of Haematology|September 27, 2022
Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patientsMaurice Swinkels, Ferdows Atiq, Petra E Bürgisser, et al.
Blood|July 18, 2025
The interleukin-33 receptor (ST2) is a novel therapeutic target to attenuate the progression of hemophilic arthropathyHeike C Hawerkamp, Aoife Yeow, Ciara Byrne, et al.
Research and Practice in Thrombosis and Haemostasis|April 14, 2025
Sexuality and bleeding in von Willebrand diseaseCalvin B van Kwawegen, Hester Pastoor, Jeroen Eikenboom, et al.
Blood Advances|April 21, 2022
Desmopressin response depends on the presence and type of genetic variants in patients with type 1 and type 2 von Willebrand diseaseFerdows Atiq, Jessica Heijdra, Fleur Snijders, et al.
Blood|December 24, 2023
Type 1 VWD classification revisited: novel insights from combined analysis of the LoVIC and WiN studiesFerdows Atiq, Robin Blok, Calvin B van Kwawegen, et al.
Blood|April 25, 2025
Clinical phenotype and pathophysiological mechanisms underlying qualitative Low VWFFerdows Atiq, Robin Blok, Calvin van Kwawegen, et al.
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