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8. Список литературы

  • l. Scharrer I. Das von Willebrand-Syndrom. Hamophilie-Blatter 1994; 28: 60-63.
  • 2. Sadler JE, Budde U, Eikenboom JC, et al. Update on the pathophysiology and classification of von Willebrand disease: a report of the subcommittee on von Willebrand factor. J Thromb. Haemost. 2006; 4 (10): 2103-2114.
  • 3. Sadler JE. A revised classification of von Willebrand disease (for the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis). Thromb. Haemost. 1994; 71: 520 -525.
  • 4. Sadler JE. Appendix II: A revised classification of Von Willebrand disease. Haemophilia 1997; 3 (Suppl. 2): 11-18.
  • 5. Rodeghiero F, Castaman G, Dini I. Epidemiological investigations of the prevalence of von Willebrand’s disease. Blood 1987; 69: 454-459.
  • 6. Budde U, Pieconka A, Will K, Schneppenheim R. Laboratory testing for von Willebrand disease: contribution of multimer analysis to diagnosis and classification. Semin. Thromb. Hemost. 2006; 32: 515-521.
  • 7. Drewke E, Krey S, Schneppenheim R, Budde U. A variant of von Willebrand disease (Type 2N) resembling phenotypically mild or moderately severe haemophilia. Infusionsther Transfusionsmed 1995; 22 (Suppl. 1): 48-50.
  • 8. Budde U, Schneppenheim R, Drewke E, et al. von Willebrand disease type Normandy in phenotypic mild haemophilia A and von Willebrand disease type 1. XXI International Congress of the World Federation of Haemophilia, 24-29 th April 1994, Mexico City: 191.
  • 9. Mazurier C. von Willebrand disease masquerading as haemophilia A. Thromb. Haemost. 1992; 67: 391-396.
  • 10. Schneppenheim R, Budde U, Krey S, et al. Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1. Thromb. Haemost. 1996; 76: 598-602
  • 11. Mazurier C, Meyer D. Factor VIII binding assay of von Willebrand factor and the diagnosis of type 2N von Willebrand disease - results of an international survey. Thromb. Haemost. 1996; 76: 270-274.
  • 12. Kasper CK. von Willebrand disease. An introductory discussion for young physicians, 2004. www.md.unc.edu/ISTH/publications/vwd monograph/VWD_monograph.pdf. Accessed March 7, 2005; 58.
  • 13. Scharrer I. Women with von Willebrand disease. Haemostasiologie 2004; 24: 44-49.
  • 14. Mannucci PM. Treatment of von Willebrand’s disease. N. Engl. J. Med. 2004; 351: 683-694.
  • 15. Martinovitz U, Schulman S, Horoszowski H, Heim M. Role of fibrin sealants in surgical procedures on patients with hemostatic disorders. Clin. Orthoped 1996; 328: 65-75
  • 16. Yanagiya K. Tanaka T, Sakamoto Y, et al Clinical application of Beriplast P in oral surgery. Hayaku Ryohoh 1992; 11(3): 174-179
  • 17. Abshire TC. Prophylaxis and von Willebrand’s disease (VWD). Thromb. Res. 2006; 118 (Suppl. 1): S3-S7.
  • 18. Paul LF, Giangrande PLF. Pregnancy in women with inherited bleeding disorders. World Federation of Haemophilia. Treatment of Hemophilia 2003; 29:9
  • 19. Caleizi C, Tsakiris DA, Behringer H, et al Two consecutive pregnancies and deliveries in patients with von Willebrand disease type 3. Haemophilia 1998; 4(6):845-849
  • 20. Diagnosis and Management of Von Willebrand Disease in The Netherlands De Wee E.M., Frank W.G. Leebeek F.W.G, Eikenboom J.C.J., Diagnosis and Management of Von Willebrand Disease in The Netherlands. Semin.Thromb.Hemost. 2011; 37(5): 480-487
  • 21. Nordic Guidelines on von Willebrand disease. Version: April 23, 2008
  • 22. Brown DL. Congenital bleeding disorders. Curr Probl Pediatr Health Care 2005; 35: 38-62.

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