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Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 08/2019, Volume 17, Issue 8, pp. 1405 - 1406
Journal Article
New England Journal of Medicine, ISSN 0028-4793, 06/2016, Volume 374, Issue 25, pp. 2497 - 2498
Journal Article
Blood Transfusion, ISSN 1723-2007, 7/2018, Volume 16, Issue 4, pp. 326 - 328
Journal Article
Thrombosis research, ISSN 0049-3848, 07/2019
von Willebrand disease (VWD) is a common autosomally inherited hemorrhagic disorder mainly associated with mucocutaneous bleeding. VWD is due to quantitative... 
Journal Article
Haemophilia, ISSN 1351-8216, 09/2019, Volume 25, Issue 5, pp. 738 - 746
Gene therapy is rapidly becoming a new therapeutic strategy for haemophilia A and B treatment. In the 1990s, studies in animal models showed that... 
haemophilia | factor IX | adeno‐associated virus | gene therapy | clinical trials | factor VIII | Hemophilia A - therapy | Humans | Genetic Therapy - methods | Coagulation factors | Animal models | Toxicity | Liver | Hemophilia | Clinical trials | Serotypes | Gene therapy | Patients | Expression vectors
Journal Article
Blood Transfusion, ISSN 1723-2007, 07/2018, Volume 16, Issue 4, pp. 326 - 328
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2016, Volume 374, Issue 6, pp. 511 - 522
Journal Article
Hematology. American Society of Hematology. Education Program, ISSN 1520-4391, 12/2016, Volume 2016, Issue 1, pp. 663 - 669
Rare bleeding disorders (RBDs) are a heterogeneous group of coagulation disorders characterized by fibrinogen, prothrombin, factors V, VII, X, XI, or XIII (FV,... 
Blood Component Transfusion | Plasma | Coagulation Protein Disorders - drug therapy | Humans | Blood Coagulation Factors - therapeutic use | Fibrinogen - therapeutic use | Rare Diseases | Coagulation Protein Disorders - diagnosis | Factor VIII - therapeutic use | Treatment of Congenital Bleeding Disorders
Journal Article
Haemophilia, ISSN 1351-8216, 05/2012, Volume 18, pp. 1 - 1
Journal Article
Haemophilia, ISSN 1351-8216, 05/2012, Volume 18, Issue 2, pp. 1 - 1
Journal Article
Haemophilia, ISSN 1351-8216, 05/2012, Volume 18, pp. 1 - 1
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 2501 - 2501
Abstract Introduction: Individuals with congenital afibrinogenemia can experience frequent and/or severe bleeding episodes (BE). Human fibrinogen concentrate... 
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 2502 - 2502
Abstract Introduction: Congenital afibrinogenemia is a rare inherited disorder characterized by an absence of plasma fibrinogen. Affected individuals have a... 
Journal Article
Blood, ISSN 0006-4971, 01/2019, Volume 133, Issue 5, pp. 415 - 424
The deficiency of fibrinogen, prothrombin, factor V (FV), FVII, FVIII, FIX, FX, FXI, and FXIII, called rare coagulation disorders (RCDs), may result in... 
FXIII DEFICIENCY | FACTOR-X CONCENTRATE | RECOMBINANT FACTOR-XIII | INHERITED BLEEDING DISORDERS | TRANEXAMIC-ACID | COAGULATION DISORDERS | FACTOR-VII DEFICIENCY | HEMATOLOGY | FRESH-FROZEN PLASMA | INTRACRANIAL HEMORRHAGE | ACTIVATED FACTOR-VII
Journal Article
Clinical Chemistry, ISSN 0009-9147, 02/2019, Volume 65, Issue 2, pp. 254 - 262
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 05/2016, Volume 374, Issue 21, pp. 2054 - 2064
Journal Article