References
- 1. Gercheva-Kyuchukova L. [Chronic myeloproliferative neoplasms]. 1st ed. Pleven: Peychinski. 2016. Bulgarian.
- 2. Lutzkanova E, Marinova I, Pavlova D, Todorov V, Tzvetkov N. [Hematology]. In: Internal diseases part II – medical student book. 1st ed. Pleven: Medical University; 2012, p. 320-34. Bulgarian.
- 3. Aftab A, Naghmi A, Hassan K. Portal vein thrombosis in a case of chronic myeloid leukemia – a rare association. JIMDC.2013;2(4):87-9.
- 4. Jain A, Gupta N, Singh T, Agarwal S. A study of haemostatic parameters in patients of chronic myeloid leukaemia. J Clin Diagn Res. 2016;10(7):0C19-0C23.
- 5. Sora F, Iurlo A, Sica S, Latagliata R, Annunziata M, Galimberti S, et al. Chronic myeloid leukaemia with extreme thrombocytosis at presentation: incidence, clinical findings and outcome. Br J Haematol. 2018;181(2):267-70.
- 6. Lad DP, Jain A, Varma S. Complications and management of coagulation disorders in leukemia patients. Dovepress. 2017;7:61-72.
- 7. Elliott MA, Tefferi A. Thrombosis and hemorrhage in polycythaemia vera and essential thrombocythaemia. Br J Haematol. 2004;128(3):275-90.
- 8. Sykes TC, Fegan C, Mosquera D. Thrombophilia, polymorphisms, and vascular disease. Mol Pathol. 2000;53(6):300-6.
- 9. Stefano V, Rossi E, Paciaroni K, Leone G. Screening for inherited thrombophilia: indications and therapeutic implications. Haematologica. 2002;87(10):1095-108.
- 10. Foy P, Moll S. Thrombophilia: 2009 update. Curr Treat Options Cardiovasc Med. 2009;11(2):114-28.
- 11. Kottke-Marchant K. Genetic polymorphisms associated with venous and arterial thrombosis. Arch Pathol Lab Med. 2002;126(3):295-304.
- 12. Antonov A, Kovacheva K, Ivanov P, Tsvetkov N, Komsa-Penkova R, Slavcheva V, et al. Genetic thrombophilic defects and risk of thrombotic complications in patients with essential thrombocythemia and polycythemia vera Part II. Contribution of the genetic thrombophilic defects to the thrombotic risk [Internet] [cited 2019 Jun 24]. Available at: https://www.researchgate.net/publication/290579253
- 13. Baglin T, Gray E, Greaves M, Hunt BJ, Keeling D, Machin S, et al. Clinical guidelines for testing for heritable thrombophilia. Br J Haematol. 2010;149(2):209-20.
- 14. Maidstone and Tunbridge Wells NHS. Guidelines for thrombophilia testing. [Internet]. [cited 2019 Jun 20]. Available from: https://www.mtw.nhs.uk/wp-content/uploads/2015/09/Guidelines-for-Thrombophilia-Testing1.pdf
- 15. Stevens SM, Woller SC, Bauer KA, Kasthuri R, Cushman M, Michael Streiff, et al. Guidance for the evaluation and treatment of hereditary and acquired thrombophilia. J Thromb Thrombolysis. 2016;41(1):154-64.
- 16. Voelkerding KV, Wu L, Williams EC, Hoffman SM, Sabatini LM, Borcherding WR, et al. Factor V R506Q gene mutation analysis by PCR-RFLP – optimization, comparison with functional testing for resistance to activated protein C, and establishment of cell line controls. Am J Clin Pathol. 1996;106(1):100-6.
- 17. Jebeleanu G, Procopciuc L. G20210A prothrombin gene mutation identified in patients with venous leg ulcers. J Cell Mol Med. 2001;5(4):397-401.
- 18. Potapov EV, Ignatenko S, Nasseri BA, Loebe M, Harke C, Bettmann M, et al. Clinical significance of PlA polymorphism of platelet GP IIb/IIIa receptors during long-term VAD support. Ann Thorac Surg. 2004;77(3):869-74.
- 19. Samani NJ, Lodwick D. Glycoprotein IIIa polymorphism and risk of myocardial infarction. Cardiovasc Res. 1997;33(3):693-7.
- 20. Khan S. Dickerman JA. Hereditary thrombophilia. Thromb J. 2006;4(15):1-17.
- 21. Bertina RM. Factor V Leiden and other coagulation risk factor mutations affecting thrombotic risk. Clin Chem. 1997;43(9):1678-83.
- 22. Zoeller B, Andreas H, García de Frutos P, Dahlback B. Thrombophilia as a multigenic disease. Haematologica. 1999;84(1):59-70.
- 23. Hoerl HD, Tabares A, Kottke-Marchant K. The diagnosis and clinical manifestations of activated protein C resistance: a case report and review of the literature. Vasc Med. 1996. 1(4):275-80.
- 24. Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet. 1995;346(8983):1133-4.
- 25. Bertina RM, Koeleman BP, Koster T, Rosendaal FR, Dirven RJ, de Ronde H. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature. 1994;369(6475):64-7.
- 26. Jensen MK, de Nully Brown P, Thorsen S, Hasselbalch HC. Frequent occurrence of anticardiolipin antibodies, Factor V Leiden mutation, and perturbed endothelial function in chronic myeloproliferative disorders. Am J Hematol. 2002;69(3):185-91.
- 27. Trifa AP, Cucuianu A, Popp RA, Coada CA, Costache RM, Militaru MS, et al. Therelationship between factor V Leiden, prothrombin G20210A, and MTHFR mutations and the first major thrombotic episode in polycythemia vera and essential thrombocythemia. Ann Hematol. 2014;93(2):203-9
- 28. Ruggeri M, Gisslinger H, Tosetto A, Rintelen C, Mannhalter C, Pabinger I, et al. Factor V Leiden mutation carriership and venous thromboembolism in polycythemia vera and essential thrombocythemia. Am J Hematol. 2002;71(1):1-6.
- 29. Afshar-Kharghan V, López JA, Gray LA, Padilla A, Borthakur G, Roberts SC, et al. Hemostatic gene polymorphisms and the prevalence of thrombotic complications in polycythemia vera and essential thrombocythemia. Blood Coagul Fibrinolysis. 2004;15(1):21-4.
- 30. Rosendaal FR, Doggen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS, et al. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost. 1998;79(4):706-8.
- 31. Leroyer C, Mercier B, Oger E, Chenu E, Abgrall JF, Férec C, et al. Prevalence of the 20210A allele of the prothrombin gene in venous thromboembolism patients. Thromb Haemost. 1998;80(1):49-51.
- 32. Rosendaal FR. Venous thrombosis: the role of genes, environment, and behavior. Hematology Am Soc Hematol Educ Program. 2005, 1-12.
- 33. Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood. 1996;88(10):3698-703.
- 34. Gisslinger H, Müllner M, Pabinger I, Heis-Vahidi-Fard N, Gisslinger B, Brichta A, et al. Mutation of the prothrombin gene and thrombotic events in patients with polycythemia vera or essential thrombocythemia: a cohort study. Haematologica. 2005;90(3):408-10.
- 35. Bray PF. Integrin polymorphisms as risk factors for thrombosis. Thromb Haemost. 1999. 82(2):337-44.
- 36. Burr D, Doss H, Cooke GE, Goldschmidt-Clermont PJ. A meta-analysis of studies on the association of the platelet PlA polymorphism of glycoprotein IIIa and risk of coronary heart disease. Stat Med. 2003;22(10):1741-60.