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(61 - 80 of 87)

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Clinical features of venous insufficiency and the risk of venous thrombosis in older people
Coagulation activation during air travel is not initiated via the extrinsic pathway
Outcome of aplastic anaemia in children. A study by the severe aplastic anaemia and paediatric disease working parties of the European group blood and bone marrow transplant
Factors associated with persistence of red blood cell antibodies in woman after pregnancies complicated by fetal alloimmune haemolytic disease treated with intrauterine transfusions
Genetic polymorphisms influencing total and gamma ' fibrinogen levels and fibrin clot properties in Africans
Optimization of the diagnostic management of clinically suspected pulmonary embolism in hospitalized patients
Storage and secretion of naturally occurring von Willebrand factor A domain variants
Low anti-RhD IgG-Fc-fucosylation in pregnancy: a new variable predicting severity in haemolytic disease of the fetus and newborn
Effect of von Willebrand factor on inhibitor eradication in patients with severe haemophilia A: a systematic review
The risk of venous thrombosis after air travel: contribution of clinical risk factors
Smoking, postmenopausal hormone therapy and the risk of venous thrombosis: a population-based, case-control study
Multiple infusions of mesenchymal stromal cells induce sustained remission in children with steroid-refractory, grade III-IV acute graft-versus-host disease
Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis
Inhibitor incidence after intensive FVIII replacement for surgery in mild and moderate haemophilia A: a prospective national study in the Netherlands
Thrombocytopenia with Absent Radii (TAR) syndrome is cause by compound inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A
Clot lysis time and the risk of myocardial infarction and ischaemic stroke in young women; results from the RATIO case-control study
Risk of cardiovascular disease in double heterozygous carriers and homozygous carriers of F5 R506Q (factor V Leiden) and F2 (prothrombin) G20210A: a retrospective family cohort study
Rapid identification of IDH1 and IDH2 mutations in acute myeloid leukaemia using high resolution melting curve analysis
The impact of bleeding history, von Willebrand factor and PFA-100 (R) on the diagnosis of type 1 von Willebrand disease: results from the European study MCMDM-1VWD

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