An SP1-binding site polymorphism in the COLIAI gene and osteoporosis in Egyptian patients with thalassemia major
Risk of recurrent venous thromboembolism according to malignancy characteristics in patients with cancer-associated thrombosis: a systematic review of observational and intervention studies
Interindividual variation in platelets and the cardiovascular response to haemorrhage in the pig
Platelet function alterations and their relation to P-selectin (CD62P) expression in children with iron deficiency anemia
Recurrent mutations and genotype–phenotype correlations in hereditary factor VII deficiency in Korea
An assessment of the utility of unselected coagulation screening in general hospital practice
Evidence for age-related differences in human fibrinogen
Genetic analysis of a pedigree with combined factor XII and factor XI deficiency
Low molecular weight heparin versus no treatment in women with previous severe pregnancy complications and placental findings without thrombophilia
Changes in von Willebrand factor and ADAMTS13 during IVF
Aurintricarboxylic acid inhibits the nuclear factor-κB-dependent expression of intercellular cell adhesion molecule-1 and endothelial cell selectin on activated human endothelial cells
Acquired protein C deficiency in a child with acute myelogenous leukemia, splenic, renal, and intestinal infarction
Diagnosis and therapeutic management in a patient with type 2B-like acquired von Willebrand syndrome
A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family
Analytic variability due to change of deficient plasma vials: application to one-stage clotting factor VIII assay