Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions
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[1] Wenman Wu,et al. Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation , 2016, Thrombosis and Haemostasis.
[2] A. Lombardi,et al. Pulmonary embolism in congenital bleeding disorders: intriguing discrepancies among different clotting factors deficiencies , 2016, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[3] P. Simioni,et al. New Prothrombin Mutation (Arg596Trp, Prothrombin Padua 2) Associated With Venous Thromboembolism , 2016, Arteriosclerosis, thrombosis, and vascular biology.
[4] H. Kiyoi,et al. The first case of antithrombin-resistant prothrombin Belgrade mutation in Japanese , 2016, Annals of Hematology.
[5] D. Radojkovic,et al. A novel prothrombin mutation in two families with prominent thrombophilia – the first cases of antithrombin resistance in a Caucasian population , 2013, Journal of thrombosis and haemostasis : JTH.
[6] Y. Miyawaki. Thrombosis from a prothrombin mutation conveying antithrombin resistance , 2013 .
[7] A. Girolami,et al. Congenital FVII deficiency and thrombotic events after replacement therapy , 2011, Journal of Thrombosis and Thrombolysis.
[8] A. Girolami,et al. Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature , 2009, Journal of Thrombosis and Thrombolysis.
[9] S. Schulte,et al. Biochemical comparison of seven commercially available prothrombin complex concentrates , 2008, International journal of clinical practice.
[10] C. Samama. Prothrombin complex concentrates: a brief review , 2008, European journal of anaesthesiology.
[11] P. Mannucci,et al. Molecular and functional characterization of a natural homozygous Arg67His mutation in the prothrombin gene of a patient with a severe procoagulant defect contrasting with a mild hemorrhagic phenotype. , 2002, Blood.
[12] A. O'marcaigh,et al. Genetic analysis and functional characterization of prothrombins Corpus Christi (Arg382-Cys), Dhahran (Arg271-His), and hypoprothrombinemia. , 1996, Blood.
[13] J. Lusher,et al. Thrombogenicity associated with factor IX complex concentrates. , 1991, Seminars in hematology.
[14] K. Mann,et al. Identification of a congenital dysthrombin, thrombin Quick. , 1980, The Journal of clinical investigation.