Author Affiliations1National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
2National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
3National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
4National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
5National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
6National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
7National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
8National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
9National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
10National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
11National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
12National Research Center for Hematology of Minzdrav of Russia 125167, Moscow, Novyy Zykovsky dr., 4
Ar M.C., Baykara O., Buyru A. N., Baslar Z. The impact of prothrombotic mutations on factor consumption in adult patients with severe hemophilia // Clin. Appl. Thromb. Hemost. 2009. 15. (6). 660–665.
Arbini A.A., Mannucci P.M., Bauer K.A. Low prevalence of the factor V Leiden mutation among “severe” hemophiliacs with a “milder” bleeding diathesis // Thromb. Haemost. 1995. 74. 1255-1258.
Barkagan Z.S. Introduction to clinical hemostasiology. Moscow: Nyudiamed-AO, 1998. 56 p. [In Russian].
Dolan G. The challenge of an ageing hemophilic population // Haemophilia. 2010. 16. 11–16.
Escuriola E.C., Halimeh S., Kurnik K., et al. Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors // Thromb. Haemost. 2001. 85. 218-220.
Fetisova I.N., Dobrolyubov A.S., Lipin M.A., Polyakov A.V. The polymorphism of folate metabolism gene and human diseases. Vestnik novykh meditsinskikh tekhnologiy = Journal of New Medical Technologies. 2007. 10. (1). 91–96. [In Russian].
Fevraleva I.S., Risinskaya N.V., Sudarikov A.B. Identification of the main markers of thrombophilia in the donor/recipient pair in bone marrow transplantation. Vestnik gematologii = Bulletin of hematology. 2018. 14. (2). 49-50. [In Russian].
Galstyan G.M., Polevodova O.A., Gavrish A.Yu., Polyanskaya T.Yu., Zorenko V.Yu., Sampiev M.S., Biryukova L.S., Model S.V., Gorgidze L.A., Savchenko V.G. Thrombotic events in patients with hemophilia. Terapevticheskiy arkhiv = Therapeutic archive. 2017. (7). 76-84 [In Russian].
Hermans C. Venous thromboembolic disease in patients with haemophilia // Thromb. Res. 2012. 130. (Suppl. 1). S50-S52.
Kashyap R., Sharma L.M., Gupta S., Saxena R., Srivastava D.N. Deep vein thrombosis in a patient with severe haemophilia A // Haemophilia. 2006. 12. 87–89.
Kopylov A.N., Elykomov V.A., Gridchina A.V. Polymorphisms of hemostatic system genes in patients with hemophilia. Yevraziyskiy soyuz uchenykh = Eurasian union of scientists. 2015. (4-7). 122-124. [In Russian].
Lee D.H., Walker I.R., Teitel J., Poon M.C., Ritchie B., Akabutu J., Sinclair G.D., Pai M., Wu J.W., Reddy S., Carter C., Growe G., Lillicrap D., Lam M., Blajchman M.A. Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A // Thromb. Haemost. 2000. 83. 387-391.
Molho P., Rolland N., Lebrun T., Dirat G., Courpied J.P., Croughs T., Duprat I., Sultan Y. Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France // Haemophilia. 2000. 6. 23-32.
Momot A.P., Roitman E.V., Elykomov V.A., Svirin P.V., Ol'khovskii I.A., Zharkov P.A., Tsyvkina L.P., Kuznetsov N.N., Serdyuk G.V., Fedorov A.V., Filipenko M.L., Boyarskikh U.A., Plyushkin V.A., Shkryabunova V.V., Lobanov Y.F. Proceedings of all-russian register «Genetic factors of thrombosis risk among people living in Russian Federation, clinical phenotyping and thrombo-prevention of thromboembolic complications in ontogenesis». Tromboz, gemostaz i reologiya = Thrombosis, hemostasis and rheology. 2010. (3). 30-78 [In Russian]
Nichols W.C., Amano K., Cacheris P.M., Figueiredo M.S., Michaelides K., Schwaab R., Hoyer L., Kaufman R.J., Ginsburg D. Moderation of hemophilia A phenotype by the factor V R506Q mutation // Blood. 1996. 88. 1183-1187.
Pollmann H., Richter H., Ringkamp H., Jurgens H. When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10-year single-centre PUP study // Eur. J. Pediatr. 1999. 158. (Suppl. 3). S166-S170.
Rainsford S.G., Hall A. A three-year study of adolescent boys suffering from haemophilia and allied disorders // Br. J. Haematol. 1973. 24. (5). 539-551.
Ramgren O. Haemophilia in Sweden. III. Symptomatology, with special reference to differences between haemophilia A and B // Acta Med. Scand. 1962. 171. 237-242.
Tuten H., Cam H., Ozdemir N., Bezgal F., Buyru N., Zulfikar B., Celkan T. Effect of prothrombotic mutations on factor consumption in children with hemophilia // Clin. Appl. Thromb. Hemost. 2013. 19. (4). 445–448.
Zoller В., Garcia F.P., Hillarp A., Dahlback B. Thrombophilia as a multigenic disease // Haematologica. 1999. 84. 59-70.