Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands study

Authors: Sterre P.E. Willems, Annet Simons, Joline L. Saes, Marjan Weiss, Sanna Rijpma, Selene Schoormans, Karina Meijer, Marjon H. Cnossen, Roger E.G. Schutgens, Nick van Es, Laurens Nieuwenhuizen, Paul L. den Exter, Ilmar C. Kruis, Nicole M.A. Blijlevens, Waander L. van Heerde, Saskia E.M. Schols

Source: Research and Practice in Thrombosis and Haemostasis, Vol 8, Iss 4, Pp 102477- (2024)

Subject Terms: blood coagulation disorders, exome sequencing, fibrinolysis, hemostasis, inherited, Diseases of the blood and blood-forming organs, RC633-647.5

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2475037924001663; https://doaj.org/toc/2475-0379

Access URL: https://doaj.org/article/571f2849b8c4407587ce0c60df94305f

Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases

Authors: Lars L. F. G. Valke, Sanna Rijpma, Danielle Meijer, Saskia E. M. Schols, Waander L. van Heerde

Source: Frontiers in Cardiovascular Medicine, Vol 9 (2022)

Subject Terms: bleeding, personalized medicine, thrombin generation, thrombosis, hemophilia, Diseases of the circulatory (Cardiovascular) system, RC666-701

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fcvm.2022.1033416/full; https://doaj.org/toc/2297-055X

Access URL: https://doaj.org/article/47eb3527adca44ef9835111ed1264125