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Journal Article
British Journal of Haematology, ISSN 0007-1048, 04/2018, Volume 181, Issue 2, pp. 173 - 182
Summary Glanzmann thrombasthenia (GT) is caused by inherited defects of the αIIbβ3 platelet glycoprotein. This bleeding disorder can be treated with platelet... 
platelet antibody | αIIbβ3 | Glanzmann thrombasthenia | rFVIIa | immunization | Immunization | Immunoglobulins | Transfusion | Complications | Glycoprotein | Antibodies | Environmental factors | Risk analysis | Patients | Risk factors | Bleeding | Literature reviews | Thermal resistance | Blood platelets | Histocompatibility antigen HLA | Platelets
Journal Article
Journal Article
British Journal of Haematology, ISSN 0007-1048, 04/2018, Volume 181, Issue 2, p. 173
Journal Article
MEDICINE, ISSN 0025-7974, 03/2016, Volume 95, Issue 11, p. e3038
von Willebrand disease (VWD) is a genetic bleeding disease due to a defect of von Willebrand factor (VWF), a glycoprotein crucial for platelet adhesion to the... 
MOLECULAR CHARACTERIZATION | DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | VWF PROPEPTIDE | MANAGEMENT | ASSAY | MCMDM-1VWD | CLINICAL MARKERS | COLLAGEN-BINDING | CLASSIFICATION | COHORT | Life Sciences | Human health and pathology
Journal Article
Haemophilia, ISSN 1351-8216, 11/2019, Volume 25, Issue 6, pp. 969 - 978
Background Acquired haemophilia (AH) is a rare bleeding disorder with significant morbidity and mortality. Most patients initially present to physicians... 
expert consensus | coagulation | Acquired haemophilia | rare bleeding disorders | Delphi methodology | diagnosis and management
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 21, pp. 2202 - 2202
Abstract Abstract 2202 Background. Glanzmann's thrombasthenia (GT) is a severe autosomal recessive bleeding disorder with defective platelet surface αIIb-β3... 
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 21, pp. 3341 - 3341
Abstract Abstract 3341 Background. Glanzmann's thrombasthenia (GT) is a severe inherited bleeding disorder with defective platelet membrane αIIbβ3. Until now... 
Journal Article