Plasma levels of plasminogen activator inhibitor-1 and bleeding phenotype in patients with von Willebrand disease

Autor: Abdul, S., Boender, J., Malfliet, J.J.M.C., Eikenboom, J., Draat, K.F. van, Mauser-Bunschoten, E.P., Meijer, K., Meris, J. de, Laros-van Gorkom, B.A.P., Bom, J.G. van der, Leebeek, F.W.G., Rijken, D.C., Willige, S.U. de, Study Grp

Publikováno v: Haemophilia, 23(3), 437-443. Wiley-Blackwell
Haemophilia, 23, 3, pp. 437-443
Haemophilia
Haemophilia, 23, 437-443
Haemophilia, 23(3), 437-443. Wiley
Haemophilia, 23(3), 437-443
Haemophilia, 23(3), 437-443. Wiley-Blackwell Publishing Ltd

Item does not contain fulltext INTRODUCTION: von Willebrand disease (VWD) is the most common inherited bleeding disorder. In VWD patients, large variations in bleeding tendency are observed, which cannot be completely explained by the variation in vo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b5cd048ab49321bce588745bcef5b6d
https://hdl.handle.net/1765/98946

Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen gamma ' levels

Autor: Willige, S.U. de, Visser, M.C.H. de, Houwing-Duistermaat, J.J., Rosendaal, F.R., Vos, H.L., Bertina, R.M.

Publikováno v: Blood, 106(13), 4176-4183. The American Society of Hematology

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bf90dabea64f41786027aa5427286f47
http://hdl.handle.net/1887/5029