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British journal of haematology, ISSN 0007-1048, 09/2019
Von Willebrand disease (VWD) is the most common inherited bleeding disorder. Most patients with mild and moderate VWD can be treated effectively with... 
Journal Article
Blood, ISSN 0006-4971, 01/2019, Volume 133, Issue 4, pp. 288 - 289
In this issue of Blood, Schneppenheim et al report the first gain-of-function (GOF) variant located in the C4 domain of von Willebrand factor (VWF) associated... 
HEMATOLOGY
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 10/2018, Volume 118, Issue 10, pp. 1690 - 1700
Abstract Long-term outcome after joint bleeds in von Willebrand disease (VWD) (von Willebrand factor activity ≤ 30 IU/dL) could differ from moderate or severe... 
Coagulation and Fibrinolysis | HAL | arthropathy | haemophilia A | Pettersson | joint bleed | von Willebrand disease | HJHS | ADULT PATIENTS | MANAGEMENT | RELIABILITY | HEALTH SCORE | MODERATE HEMOPHILIA | PERIPHERAL VASCULAR DISEASE | QUALITY-OF-LIFE | PROPHYLAXIS NETWORK | HEMATOLOGY | ASSOCIATION | ACTIVITIES LIST
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 10/2019, Volume 19, Issue 10, pp. 1624 - 1631
Abstract Background  Many proteins bind to fibrin during clot formation in plasma. We previously identified by mass spectrometry the most abundant proteins... 
Coagulation and Fibrinolysis
Journal Article
Haemophilia, ISSN 1351-8216, 01/2019, Volume 25, Issue 1, pp. 162 - 169
Background Both one‐stage (OSA) and chromogenic substrate assays (CSA) are used to measure factor VIII (FVIII) activity. Factors explaining analytical... 
factor VIII | haemophilia A | FVIII measurements | DIAGNOSIS | APTT | MANAGEMENT | GUIDELINES | SENSITIVITY | PARTIAL THROMBOPLASTIN TIME | HEMATOLOGY | Coagulation factors | Variation | Standardization | Hemophilia | Quality control
Journal Article
New England Journal of Medicine, ISSN 0028-4793, 02/2017, Volume 376, Issue 7, pp. 701 - 701
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 04/2017, Volume 64, Issue 4, p. n/a
Journal Article
International Journal of Clinical Pharmacy, ISSN 2210-7703, 6/2019, Volume 41, Issue 3, pp. 691 - 699
Background Anticoagulant therapy is associated with a high risk of complications. Adherence to anticoagulant therapy protocols may lower this risk but... 
Adherence | The Netherlands | Medicine & Public Health | Pharmacy | Internal Medicine | Complex intervention | Anticoagulant therapy | Antithrombotic stewardship | Medical personnel | Intervention | Drugs | Dosing | Anticoagulants | Therapy | Statistical analysis | Complications | Physicians | Regression analysis | Patients | Adhesion | Guidelines | Confidence intervals | Heparins
Journal Article
Haemophilia : the official journal of the World Federation of Hemophilia, ISSN 1351-8216, 09/2019
In patients with haemophilia A (HA) perioperative dosing of factor VIII (FVIII) concentrate is based on body weight, historical FVIII level, in vivo recovery... 
Journal Article
Atherosclerosis, ISSN 0021-9150, 02/2018, Volume 269, pp. 144 - 150
It is as yet unknown whether antithrombin levels are associated with arterial thromboembolism (ATE) at a young age. To investigate the association between... 
CARDIAC & CARDIOVASCULAR SYSTEMS | THROMBOSIS | PROGNOSIS | THROMBOPHILIA | ACUTE MYOCARDIAL-INFARCTION | ITALIAN PROJECT | ADULTS | ATHEROSCLEROSIS | PERIPHERAL VASCULAR DISEASE | CORONARY-HEART-DISEASE | ISCHEMIC-STROKE | DEFICIENCY
Journal Article
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 08/2015, Volume 114, Issue 3, pp. 639 - 644
Haemophilia A is an X-linked inherited, rare bleeding disorder, caused by a deficiency of coagulation factor VIII (FVIII). Previous studies in prophylactic... 
Haemophilia therapy | Factor concentrates | Pharmaco-kinetics | Bayesian analysis | Factor VIII
Journal Article