Rationale for individualizing haemophilia care
Plasma factor XI and XII activity in patients with slow coronary flow
How medical treatment affects mean platelet volume as a cardiovascular risk marker in polycystic ovary syndrome?
Maternal low-level somatic mosaicism of Cys155Tyr of F9 in severe hemophilia B
Association study of methylenetetrahydrofolate reductase C677T mutation with cerebral venous thrombosis in an Iranian population
Influence of P2Y12 polymorphisms on platelet activity but not ex-vivo antiplatelet effect of ticagrelor in healthy Chinese male subjects
Novel fibrinogen mutations (Aα17Gly→Cys and Aα381Ser→Phe) occurring with a 312Thr→Ala polymorphism
Effects of febuxostat on platelet-derived microparticles and adiponectin in patients with hyperuricema
Factor XII full and partial null in rat confers robust antithrombotic efficacy with no bleeding
Clinical characteristics of in-situ pulmonary artery thrombosis in Korea
First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran
Nonacog alfa
Thrombomodulin gene proximal promoter polymorphisms in premature acute coronary syndrome patients in Bahrain
Rivaroxaban and apixaban in orthopaedics
Meta-analysis on efficacy and safety of new oral anticoagulants for venous thromboembolism prophylaxis in elderly elective postarthroplasty patients
Challenges of the management of severe hemophilia A with inhibitors
A rare combination
Acute myocardial infarction as a finding of acute promyelocytic leukemia–related coagulation disorder
Extreme warfarin hypersensitivity after oophorectomy
Factor VII Tokushima
Intracardiac echocardiography for immediate detection of intracardiac thrombus formation
Correction of factor XI deficiency by liver transplantation
Exsanguinating bleeding following tooth extraction in a 12-year-old girl
Acquired factor VIII inhibitor and subsequent development of non-Hodgkin's lymphoma
Is the time in therapeutic range using the ratio of tests equivalent to the Rosendaal method?
Severe female hemophilia A patient caused by a nonsense mutation (p.Gln1686X) of F8 gene combined with skewed X-chromosome inactivation
Yes or no for secondary prophylaxis in afibrinogenemia?