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Research and Practice in Thrombosis and Haemostasis|July 30, 2024
Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands studySterre P E Willems, Annet Simons, Joline L Saes, et al.Hemasphere|June 24, 2022
Importance of Genotyping in von Willebrand Disease to Elucidate Pathogenic Mechanisms and Variability in PhenotypeFerdows Atiq, Johan Boender, Waander L van Heerde, et al.Journal of Thrombosis and Haemostasis : JTH|March 8, 2025
Bleeding symptoms in persons with rare bleeding disorders and a heterozygous genotype: data from the Rare Bleeding Disorders in the Netherlands studySterre P E Willems, Marjon H Cnossen, Nick van Es, 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.BMC Neurology|September 22, 2011
Risk factors and prognosis of young stroke. The FUTURE study: a prospective cohort study. Study rationale and protocolLoes C A Rutten-Jacobs, Noortje A M Maaijwee, Renate M Arntz, et al.Frontiers in Immunology|March 8, 2024
The spectrum of neutralizing and non-neutralizing anti-FVIII antibodies in a nationwide cohort of 788 persons with hemophilia AIlja Oomen, Marieke Verhagen, Mariarosaria Miranda, et al.Blood|April 25, 2025
Clinical phenotype and pathophysiological mechanisms underlying qualitative Low VWFFerdows Atiq, Robin Blok, Calvin van Kwawegen, et al.Blood|August 9, 2013
Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia ACorien L Eckhardt, Alice S van Velzen, Marjolein Peters, et al.Pageof 6