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New England Journal of Medicine, ISSN 0028-4793, 02/2017, Volume 376, Issue 7, pp. 701 - 702
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
Blood, ISSN 0006-4971, 02/2016, Volume 127, Issue 5, pp. 538 - 545
Human α2-antiplasmin (α2AP, also called α2-plasmin inhibitor) is the main physiological inhibitor of the fibrinolytic enzyme plasmin. α2AP inhibits plasmin on... 
Amino Acid Sequence | Sequence Alignment | Humans | alpha-2-Antiplasmin - chemistry | Models, Molecular | Molecular Sequence Data | Protein Conformation | Protein Processing, Post-Translational | alpha-2-Antiplasmin - genetics | alpha-2-Antiplasmin - metabolism
Journal Article
Thrombosis Research, ISSN 0049-3848, 04/2012, Volume 129, Issue 1, pp. S88 - S92
Patients diagnosed with multiple myeloma have an increased risk of venous thrombosis. This may be due to various risk factors, including disease specific... 
Arterial thrombosis | Anticoagulants | LMWH | Aspirin | Warfarin | Multiple myeloma | Venous thrombosis | Anticoagulants (Medicine) | Thrombosis | Risk factors | Blood clot
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 274 - 274
Abstract Background: Patients with multiple myeloma (MM) are at a 9-fold increased risk of venous thromboembolism (VTE). Mechanisms underlying the increased... 
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 3789 - 3789
Abstract Background Recurrent joint bleeds are the main cause of joint deterioration (hemophilic arthropathy) in patients with hemophilia. To what extent... 
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 2638 - 2638
Abstract Background Platelet concentrates (PCs) are stored at room temperature to preserve their biological activity. To minimize the risk of bacterial... 
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 04/2017, Volume 64, Issue 4, p. e26276
Journal Article
Molecular Therapy - Methods & Clinical Development, ISSN 2329-0501, 12/2019, Volume 15, pp. 170 - 178
As gene transfer with adeno-associated virus (AAV) vectors is starting to enter clinical practice, this review examines the impact of vector capsid choice in... 
Journal Article
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 3510 - 3510
Abstract Background Hemophilia A (HA) is caused by a clotting factor VIII (FVIII) deficiency, resulting in spontaneous bleeding and bleeding after minor trauma... 
Journal Article
Blood, ISSN 0006-4971, 11/2017, Volume 130, Issue 21, pp. 2241 - 2242
In this issue of Blood, Lavin et al report their study of 126 patients who presented at the Irish Reference Center for Bleeding Disorders with bleeding... 
PHENOTYPE | DIAGNOSIS | MANAGEMENT | TYPE-1 | HEMATOLOGY | VON-WILLEBRAND-DISEASE | von Willebrand Diseases | von Willebrand Factor | Hemorrhage | Hemorrhagic Disorders | Humans
Journal Article
Blood, ISSN 0006-4971, 03/2018, Volume 131, Issue 9, pp. 1022 - 1031
Gene therapy for hemophilia B aims to ameliorate bleeding risk and provide endogenous factor IX (FIX) activity/synthesis through a single treatment,... 
CLINICAL-TRIAL | EFFICACY | REFERENCE-STANDARD MATERIAL | SAFETY | LIVER | PADUA | HEMATOLOGY | TYPE-2 | Thrombosis and Hemostasis
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 11/2016, Volume 375, Issue 21, pp. 2067 - 2080
Von Willebrand's disease is the most common inherited bleeding disorder and is generally transmitted as an autosomal dominant trait. It is mainly associated... 
Von Willebrand's disease | Genetic disorders | Hematology | Mucosa | Surgery | Mutation | Blood diseases | Trauma | Bleeding
Journal Article