A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding
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[1] D. Grobbee,et al. The Utility of the Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Assay in Detecting Abnormalities in Lipid Metabolism and Cardiovascular Risk in an HIV-Infected South African Cohort , 2019, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.
[2] Y. Kanai,et al. A paradoxical thrombogenic mutation in factor II at the target site of arthropod bleeding toxin. , 2019, European journal of medical genetics.
[3] S. Ferrari,et al. The Dysprothrombinemias due to Arg596 Mutations: A Conundrum With No Bleeding Tendency and Venous Thrombosis due to Antithrombin Resistance , 2019, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.
[4] A. Takagi,et al. Familial pulmonary thromboembolism with a prothrombin mutation and antithrombin resistance. , 2018, Journal of cardiology cases.
[5] S. Ferrari,et al. Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study , 2017, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[6] D. Radojkovic,et al. Clinical and biochemical characterization of the prothrombin Belgrade mutation in a large Serbian pedigree: new insights into the antithrombin resistance mechanism , 2017, Journal of thrombosis and haemostasis : JTH.
[7] P. Simioni,et al. New Prothrombin Mutation (Arg596Trp, Prothrombin Padua 2) Associated With Venous Thromboembolism , 2016, Arteriosclerosis, thrombosis, and vascular biology.
[8] H. Kiyoi,et al. The first case of antithrombin-resistant prothrombin Belgrade mutation in Japanese , 2016, Annals of Hematology.
[9] 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.
[10] R. De Cristofaro,et al. Congenital Prothrombin Deficiency: An Update , 2013, Seminars in Thrombosis & Hemostasis.
[11] S. Nair,et al. Molecular defect of 'Prothrombin Amrita': substitution of arginine by glutamine (Arg553 to Gln) near the Na(+) binding loop of prothrombin. , 2013, Blood cells, molecules & diseases.
[12] T. Naoe,et al. Thrombosis from a prothrombin mutation conveying antithrombin resistance. , 2012, The New England journal of medicine.
[13] A. Bertomoro,et al. Congenital deficiencies and abnormalities of prothrombin. , 1998, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[14] A. O'marcaigh,et al. Genetic analysis and functional characterization of prothrombins Corpus Christi (Arg382-Cys), Dhahran (Arg271-His), and hypoprothrombinemia. , 1996, Blood.
[15] S. J. Degen,et al. Prothrombin Frankfurt: A Dysfunctional Prothrombin Characterized by Substitution of Glu-466 by Ala , 1995, Thrombosis and Haemostasis.
[16] H. Asakura,et al. Prothrombin Himi: a compound heterozygote for two dysfunctional prothrombin molecules (Met-337-->Thr and Arg-388-->His). , 1992, Blood.
[17] S. Iwanaga,et al. Prothrombin Salakta: substitution of glutamic acid-466 by alanine reduces the fibrinogen clotting activity and the esterase activity. , 1992, Biochemistry.
[18] A. Quick. CONGENITAL HYPOPROTHROMBINÆMIA AND PSEUDO-HYPOPROTHROMBINÆMIA , 1947 .
[19] A. Quick. Congenital hypoprothrombinaemia and pseudo-hypoprothrombinaemia. , 1947, Lancet.