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The New England Journal of Medicine, ISSN 0028-4793, 08/2018, Volume 379, Issue 9, pp. 880 - 882
Hemophilia A is an X-linked disorder caused by defective factor VIII, which until now has involved factor VIII replacement to treat and prevent bleeding in... 
MEDICINE, GENERAL & INTERNAL | BISPECIFIC ANTIBODY | EMICIZUMAB | HEMOPHILIA-A MODEL | BLEEDS | Clinical trials | Treatment outcome | Drug therapy | Analysis | Hemophilia | Coagulation factors | Intravenous administration | Pain | Cytokines | Hemostasis | Muscles | FDA approval | Thrombosis | Patients | Mimicry
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 2469 - 2469
Abstract Background: Von Willebrand disease (VWD) is the single most common congenital bleeding disorder, affecting 1% of the population and characterized by... 
Journal Article
Blood, ISSN 0006-4971, 03/2016, Volume 127, Issue 10, pp. 1222 - 1224
In this issue of Blood, Chen et al demonstrate that platelets expressing factor VIII (FVIII) shield FVIII from immune detection. In the naive FVIIInull... 
HALF-LIFE | THERAPY | INHIBITOR | HEMATOLOGY | HEMOPHILIA-A | Factor VIII - immunology | Autoantibodies - immunology | Animals | Blood Platelets - immunology | Platelet Transfusion | Hemophilia A - immunology | Blood Coagulation Factor Inhibitors - immunology
Journal Article
Hematology, ISSN 1520-4391, 12/2017, Volume 2017, Issue 1, pp. 605 - 609
Inhibitor formation is among the most severe complications of hemophilia treatment. With a cumulative lincidence of 30% in those with severe hemophilia A and... 
FACTOR XA | BISPECIFIC ANTIBODY | (SUPER)FACTOR VA | VARIANTS | HEMOPHILIA-A | COAGULATION | TFPI | BLOCKING | HEMATOLOGY | FACTOR-FACTOR VIIA | EDUCATION, SCIENTIFIC DISCIPLINES | ACE910
Journal Article
Haemophilia, ISSN 1351-8216, 05/2019, Volume 25, Issue 3, pp. e199 - e203
Journal Article
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 760 - 760
Background: Orthotopic liver transplant (OLTx) is increasingly being performed in hemophilia patients with cirrhosis or hepatocellular carcinoma (HCC).... 
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 2584 - 2584
Introduction: Little is known about aging in von Willebrand disease (VWD). While it has been well established that von Willebrand factor (VWF) levels increase... 
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 1179 - 1179
Abstract Background:Von Willebrand disease (VWD) is a common congenital bleeding disorder, caused by defective or deficient von Willebrand factor (VWF), and... 
Journal Article
Hematology. American Society of Hematology. Education Program, ISSN 1520-4391, 12/2017, Volume 2017, Issue 1, pp. 605 - 609
Inhibitor formation is among the most severe complications of hemophilia treatment. With a cumulative incidence of ∼30% in those with severe hemophilia A and... 
The Changing Landscape of Hemophilia Therapy
Journal Article
The Lancet Haematology, ISSN 2352-3026, 06/2019, Volume 6, Issue 6, pp. e286 - e287
Journal Article
2016, ISBN 9783319303505
This book, in Q&A format, addresses a wide range of clinically relevant topics and issues in Nonmalignant Hematology, or “Benign Hematology,” with a view to... 
Medicine | Pediatrics | Nursing | Hematology | Oncology
Web Resource
2016, ISBN 9783319303505
This book, in Q&A format, addresses a wide range of clinically relevant topics and issues in Nonmalignant Hematology, or “Benign Hematology,” with a view to... 
Medicine | Pediatrics | Nursing | Hematology | Oncology
Web Resource
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 3531 - 3531
Abstract Introduction: Inhibitor formation affects approximately 30% of individuals with severe hemophilia A. The eradication of inhibitors using immune... 
Journal Article
Blood, ISSN 0006-4971, 07/2017, Volume 130, Issue 3, pp. 240 - 241
In this issue of Blood, Hudecova and colleagues describe a simple, noninvasive assay for prenatal detection of hemophilia by droplet digital polymerase chain... 
HEMATOLOGY | CARRIERS | HEMOPHILIA-A | LIFE
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2015, Volume 373, Issue 4, pp. 389 - 391
Journal Article
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 3512 - 3512
Abstract Background: Inhibitor formation is among the most serious complications of hemophilia A. These alloantibodies are directed against foreign infused... 
Journal Article
Blood, ISSN 0006-4971, 12/2014, Volume 124, Issue 21, pp. 2825 - 2825
Abstract Background: While epistaxis and menorrhagia represent the most common symptoms in those with von Willebrand disease (VWD), postoperative and... 
Journal Article
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