1. Зозуля Н.И. Диагностика и лечение ингибиторной формы гемофилии: Автореф. дис...д-ра мед. наук. М., 2010
2. Момот А.П. Принципы и алгоритмы клинико-лабораторной диагностики. СПб. 2006.
3. Протокол ведения больных «Гемофилия». Проблемы стандартизации в здравоохранении 2006, с. 18 - 74
4. Спирин, М. В., Галстян, Г. М., Полеводова, О. А., Кудлай, Д. А., Полянская, Т. Ю., Зозуля, Н. И., Троицкая, В. В. (2017). Периферические имплантируемые центральные венозные катетеры для обеспечения длительного сосудистого доступа у больных с геморрагическим синдромом. Гематология И Трансфузилогия, 64(4), 203-210. http://doi.org/http://dx.doi.org/10.18821/0234-5730-2017-62-4
5. BIV Astermark J, Petrini P, Tengborn L, et al. Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized. Br J Haematol 1999;105:1109-13
6. Canadian Hemophilia Standards Group. Canadian Comprehensive Care Standards for Hemophilia and Other Inherited Bleeding Disorders, First Edition, June 2007
7. Castaman G, Mancuso ME, Giacomelli SH, et al. Molecular and phenotypic determinants of the response to desmopressin in adult patients with mild hemophilia A. J Thromb Haemost 2009;7(11):1824-31
8. Collins Peter W, Chalmers E, Daniel P. Hart DP, at al. Diagnosis and treatment of. factor VIII and IX inhibitors in congenital haemophilia: (4th edition). British Journal оФ. Haematology. Volume 160, Issue 2, pages 153-170, January 2013
9. Colvin BT, Astermark J, Fischer K, Gringeri A, Lassila R, Schramm W, Thomas A, Ingerslev J; Inter Disciplinary Working Group. European principles oФ. haemophilia care. Haemophilia 2008;14(2):361-74
10. De Moerloose P, Fischer K, Lambert T et al. Recommendations for assessment, monitoring and follow-up of patients with haemophilia. Haemophilia 2012; 18: 319-25
11. Fonseca, A., Nagel, K., Decker, K., Pukulakatt, M., Pai, M., Walton, M., & Chan, A. K. C. (2016). Central venous access device insertion and perioperative management of patients with severe haemophilia A: a local experience. Blood Coagulation & Fibrinolysis, 27(2), 156-159
12. Franchini M, Zaffanello M, Lippi G. The use of desmopressin in mild hemophilia A. Blood Coagul fibrinolysis 2010;21(7):615-9
13. Johnsen, Jill M. et al "Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative." Blood Advances 1.13 (2017): 824-834
14. Golestani M, Eshghi P, Rasekh HR, Cheraghali AM, Salamzadeh J, Imani A. Comparison of bypassing agents in bleeding reduction in treatment of bleeding episodes in patients with haemophilia and inhibitors. Iran Red Crescent Med J. 2014;16(12):e24551
15. Gouw, Samantha C. et al "F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis." Blood 119.12 (2012): 2922-2934
16. Guidelines for the management of hemophilia. 2nd edition. Доступно в интернете по адресу www.WFH.org
17. Mannucci P.M., Garagiola I. Factor VIII products in haemophilia A: one size fits all? Thromb Haemost 2015; 113(05): 911-914
18. Nilsson IM, Berntorp E, Lofqvist T, Pettersson H. Twenty-five years’ experience of prophylactic treatment in severe haemophilia A and B. J Intern Med 1992;232(1):25-32
19. Oldenburg J, Mahlangu JN, Kim B, Schmitt C, Callghan MU, Young G, Santagostino E,Kruse-Jarres R, Negrier C, Kessler C, Valente N, Asikanius E, Levy GG, Windyga J, Shima M. Emicizumab Prophylaxis in Hemophilia A with Inhibitors. N Engl J Med (2017) 377 (9)Л809-818
20. Richards M, Williams M, Chalmers E, at al. A United Kingdom Haemophilia Centre Doctors’ Organization guideline approved by the British Committee for Standards in Haematology: guideline on the use of prophylactic factor VIII concentrate in children and adults with severe haemophilia A. British Journal of Haematology. Volume 149, Issue 4, pages 498-507, May 2010
21. Srivastava A, et al. Guidelines for the management of hemophilia (WFH). Haemophilia 2013: 19; e1-e47
22. Stonebraker JS, Bolton-Maggs PH, Soucie JM, Walker I, Brooker M. A study of variations in the reported haemophilia A prevalence around the world. Haemophilia 2010;16(1):20-32
23. Pediatrics Nov Ullman A.J., Marsh N., Mihala G. et al. Complications of Central Venous Access Devices: A Systematic Review. 2015, 136 (5) e1331-e1344
24. Valentino, L., Ewenstein, B., Navickis, R. J., & Wilkes, M. M. (2004). Central venous access devices in haemophilia. Haemophilia, 10(2), 134-46