Study of the fibrinolytic process in a patient with antiphospholipid syndrome
Contribution of platelets indices in the development of contrast-induced nephropathy
Does saline resuscitation affect mechanisms of coagulopathy in critically ill trauma patients? An exploratory analysis
Comprehensive study on laboratory biomarkers for prediction and diagnosis of deep venous thrombosis
Frequency of vascular and pregnancy morbidity in patients with low vs. moderate-to-high titers of antiphospholipid antibodies
Effects of anticoagulant therapy on pregnancy outcomes in patients with thrombophilia and previous poor obstetric history
Roles of the red cell distribution width and neutrophil/lymphocyte ratio in predicting thrombolysis failure in patients with an ST-segment elevation myocardial infarction
Arthroscopic debridement for ankle haemophilic arthropathy
Mean platelet volume in euthyroid patients with Hashimoto's thyroiditis
Vitamin D levels in children with severe hemophilia A
Experimental model of hyperfibrinolysis designed for rotational thromboelastometry in children with congenital heart disease
The level of red cell distribution width cannot identify deep vein thrombosis in patients undergoing total joint arthroplasty
Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndrome
Impact of thrombophilic genes mutations on thrombosis risk in Egyptian nonmetastatic cancer patients
Estriol-induced fibrinolysis due to the activation of plasminogen to plasmin by nitric oxide synthesis in platelets
Prevention of bleeding and hemorrhagic complications in surgical patients with inherited factor VII deficiency
Acquired factor VII deficiency associated with acute myeloid leukemia
Effective treatment with para-aminomethylbenzoic acid for chronic disseminated intravascular coagulation associated with aortic dissection
Congenital amegakaryocytic thrombocytopenia
Cerebral venous thrombosis in young adult with familial protein S deficiency
Antithrombotic therapy in a patient with mild haemophilia A and atrial fibrillation
Prenatal diagnosis in a family with purfura fulminans
Plasminogen activator inhibitor type 1 deficiency revealed by severe bleeding after prostatectomy in a 76-year-old male
Achilles’ heel of Aristotle
Factor X deficiency associated with compound heterozygosity involving a novel missense mutation at codon 38 from Val (GTC) to Leu (CTC) in exon 2
A case of congenital afibrinogenemia complicated with thromboembolic events that required repeated amputations