HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

platelet type Von Willebrand disease

An autosomal dominant bleeding disorder characterized by abnormally enhanced binding of VON WILLEBRAND FACTOR by the PLATELET GLYCOPROTEIN GPIB-IX COMPLEX. Mutations in the GP1BA gene have been identified. OMIM: 177820
Also Known As:
Von Willebrand disease, platelet type; Platelet-type Von Willebrand disease; Pseudo-Von Willebrand disease; Von Willebrand Disease, Platelet-Type
Networked: 37 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Related Diseases

1. Hemorrhage
2. Thrombocytopenia (Thrombopenia)
3. Type 2 von Willebrand Disease
4. Bernard-Soulier Syndrome (Giant Platelet Syndrome)
5. Vascular System Injuries

Experts

1. Gresele, Paolo: 3 articles (12/2022 - 06/2010)
2. Auton, Matthew: 2 articles (12/2022 - 12/2019)
3. Bury, Loredana: 2 articles (12/2022 - 01/2019)
4. Mezzasoma, Anna Maria: 2 articles (12/2022 - 06/2010)
5. Moon-Tasson, Laurie: 2 articles (12/2022 - 12/2019)
6. Tischer, Alexander: 2 articles (12/2022 - 12/2019)
7. Russell, Susan: 2 articles (12/2009 - 02/2008)
8. Ware, Jerry: 2 articles (12/2009 - 02/2008)
9. Cruz, Miguel A: 2 articles (06/2005 - 12/2003)
10. López, José A: 2 articles (06/2005 - 12/2003)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to platelet type Von Willebrand disease:
1. asialo-von Willebrand FactorIBA
2. von Willebrand FactorIBA
3. Platelet Membrane GlycoproteinsIBA
4. RistocetinIBA
5. Platelet Glycoprotein GPIb-IX Complex (Glycoprotein Ib)IBA
6. Glycoproteins (Glycoprotein)IBA
7. Factor VIII (Coagulation Factor VIII)IBA
8. Monoclonal AntibodiesIBA
9. IntegrinsIBA
10. ThrombinFDA Link

Therapies and Procedures

1. Transjugular Intrahepatic Portasystemic Shunt
2. Therapeutics