Physical activity in individuals with haemophilia and experience with recombinant factor VIII Fc fusion protein and recombinant factor IX Fc fusion protein for the treatment of active patients : a literature review and case reports
Bromelain has paradoxical effects on blood coagulability : a study using thromboelastography
Use of recombinant activated factor VII for acute bleeding episodes in acquired hemophilia : final analysis from the Hemostasis and Thrombosis Research Society Registry acquired hemophilia study
Assessment of acquired hemophilia patient demographics in the United States : the Hemostasis and Thrombosis Research Society Registry
Efficacy and toxicity of Samen-ista emulsion on treatment of cutaneous and mucosal bleeding
Autumn season birth is associated with a lower frequency of diagnosis of unprovoked deep vein thrombosis in the emergency department
Enoxaparin chains stored during chronic treatment are mobilized by a bolus of unfractionated heparin : insights from the STACKENOX study
Plasma factor XIII level variations during menstrual cycle
Association of TNF-α −308G>A and TNF-β +252A>G genes polymorphisms with primary immune thrombocytopenia : a North Indian study
Moderate-intensity exercise improves the thromboelastography coagulation index in children with severe hemophilia A
Thromboelastographic predictors of venous thromboembolic events in critically ill patients : are we missing something?
Surgery in patients with von Willebrand disease
Activation of the tissue factor-dependent extrinsic pathway and its relation to JAK2 V617F mutation status in patients with essential thrombocythemia
Acquired factor inhibitor in a patient with monoclonal gammopathy of undetermined significance responding to rituximab
Successful use of eltrombopag in a child with refractory immune thrombocytopenia : case study and literature review
Nonactivated thromboelastometry able to detect fibrinolysis in contrast to activated methods (EXTEM, INTEM) in a bleeding patient
Pulmonary embolism, deep vein thrombosis and recurrent bone cysts in a patient with hypereosinophilic syndrome
Von Willebrand disease in sub-Saharan Africa : a first severe case reported in Cameroon
A protein C and plasminogen compound heterozygous mutation and a compound heterozygote of protein C in two related Chinese families