[1. Shetty S, Kasatkar P, Ghosh K. Pathophysiology of acquired von Willebrand disease: a concise review. Eur J Haematol 2011; 87(2):99–106. DOI: 10.1111/j.1600-0609.2011.01636.x10.1111/j.1600-0609.2011.01636.x]Search in Google Scholar
[2. Franchini M, Lippi G. Acquired von Willebrand syndrome: an update. Am J Hematol. 2007;82(5):368–75. DOI: 10.1002/ajh.2083010.1002/ajh.20830]Search in Google Scholar
[3. Mohri H. Acquired von Willebrand syndrome: Its pathophysiology, laboratory features and management. J Thromb Thrombolysis. 2003;15(3):141–9. DOI: 10.1023/B:THRO.0000011369.70824.e610.1023/B:THRO.0000011369.70824.e6]Search in Google Scholar
[4. Mohri H. Acquired von Willebrand syndrome: features and management. Am J Hematol. 2006;81(8):616-23. DOI: 10.1002/ajh.2045510.1002/ajh.20455]Search in Google Scholar
[5. Tiede A, Rand JH, Budde U, Ganser A, Federici AB. How I treat the acquired von Willebrand syndrome. Blood. 2011;117(25):6777-85. DOI: 10.1182/blood-2010-11-29758010.1182/blood-2010-11-297580]Search in Google Scholar
[6. Federici AB, Rand JH, Bucciarelli P, Budde U, Van Genderen PJJ, Mohri H, et al. Acquired von Willebrand syndrome: data from an International registry. Thromb Haemost. 2000;84(2):345-9.]Search in Google Scholar
[7. Tiede A. Diagnosis and treatment of acquired von Willebrand syndrome. Thrombosis Research. 2012;130(Suppl. 2):S2–S6. DOI: 10.1016/S0049-3848(13)70003-310.1016/S0049-3848(13)70003-3]Search in Google Scholar
[8. Federici AB. Budde U, Castaman G, Rand HR, Tiede A. Current diagnostic and therapeutic approaches to patients with acquired von Willebrand syndrome: a 2013 update. Semin Thromb Hemost. 2013;39(2):191-201. DOI: 10.1055/s-0033-133486710.1055/s-0033-133486723397553]Search in Google Scholar
[9. Boissier E, Darnige L, Dougados J, Arlet JB, Dupeux S, Georgin-Lavialle S, et al. Acquired von Willebrand syndrome: A case series of nine patients and literature review. Rev Med Interne. 2014;35(3):154-9. DOI: 10.1016/j.revmed.2013.02.03910.1016/j.revmed.2013.02.03923746599]Search in Google Scholar
[10. Budde U, Bergmann F, Michiels JJ. Acquired von Willebrand syndrome: experience from 2 years in a single laboratory compared with data from the literature and an international registry. Semin Thromb Hemost. 2002;28(2):227-38. DOI: 10.1055/s-2002-2782410.1055/s-2002-2782411992245]Search in Google Scholar
[11. Federici AB, Budde U, Rand JH. Acquired von Willebrand syndrome 2004: International registry. Hamostaseologie. 2004;24(1):50–5.10.1055/s-0037-1619606]Search in Google Scholar
[12. Federici AB. Acquired von Willebrand syndrome: an underdiagnosed and misdiagnosed bleeding complication in patients with lymphoproliferative and myeloproliferative disorders. Semin Hematol 2006;43(1 Suppl 1):S48–58. DOI: 10.1053/j.seminhematol.2005.11.00310.1053/j.seminhematol.2005.11.00316427386]Search in Google Scholar
[13. Vincentelli A, Susen S, Le Tourneau T, Six I, Fabre O, Juthier F, et al. Acquired von Willebrand syndrome in aortic stenosis. N Engl J Med. 2003;349(4):343-9. DOI: 10.1056/NEJMoa02283110.1056/NEJMoa02283112878741]Search in Google Scholar
[14. Fukumoto Y. Impact of acquired von Willebrand syndrome in severe aortic stenosis. J Atheroscler Thromb. 2015;22(11):1113-4. DOI: 10.5551/jat.ED02410.5551/jat.ED02426370453]Search in Google Scholar
[15. Tamura T, Horiuchi H, Imai M, Tada T, Shiomi H, Kuroda M, et al. Unexpectedly High Prevalence of Acquired von Willebrand Syndrome in Patients with Severe Aortic Stenosis as Evaluated with a Novel Large Multimer Index. J Atheroscler Thromb. 2015 Nov 2;22(11):1115-23. DOI: 10.5551/jat.3080910.5551/jat.3080926269004]Search in Google Scholar
[16. Zoghi B, Shaughnessy P, Lyons RM, Helmer R, Bachier C, LeMaistre CF. Treatment of Acquired von Willebrand Syndrome and Prevention of Bleeding Postautologous Stem Cell Transplant during Severe Pancytopenia with IVIG. Case Rep Hematol. 2015;2015:809313. DOI: 10.1155/2015/80931310.1155/2015/809313439896125922770]Search in Google Scholar
[17. Franchini M, Castaman G, Coppola A, Santoro C, Zanon E, Di Minno G, et al. Acquired inhibitors of clotting factors: AICE recommendations for diagnosis and management. Blood Transfus. 2015;13(3):498-513.]Search in Google Scholar
[18. Lancelloti S, Dragani A, Ranalli P, Petrucci G, Basso M, Tartaglione R, et al. Qualitative and quantitative modifications of von Willebrand factor in patients with essential thrombocythemia and controlled platelet count. J Thromb Haemost. 2015;13(7):1226-37. DOI: 10.1111/jth.1296710.1111/jth.1296725876231]Search in Google Scholar
[19. Scrobohaci ML, Daniel MT, Levy Y, Marolleau JP, Brouet JC. Expression of GpIb on plasma cells in a patient with monoclonal IgG and acquired von Willebrand disease. Br J Haematol. 1993;84(3):471–5. DOI: 10.1111/j.1365-2141.1993.tb03103.x10.1111/j.1365-2141.1993.tb03103.x8217799]Search in Google Scholar
[20. Pareti FI, Lattuada A, Bressi C, Zanobini M, Sala A, Steffan A, Ruggeri ZM. Proteolysis of von Willebrand factor and shear stress-induced platelet aggregation in patients with aortic valve stenosis. Circulation. 2000;102(11):1290–5. DOI: 10.1161/01.CIR.102.11.129010.1161/01.CIR.102.11.129010982545]Search in Google Scholar
[21. Kruse-Jarres R. Acquired bleeding disorders in the elderly. Hematology Am Soc Hematol Educ Program. 2015. 2015(1):231-6. DOI: 10.1182/asheducation-2015.1.23110.1182/asheducation-2015.1.23126637727]Search in Google Scholar
[22. Pipe N, Goldenberg N. Acquired Disorders of Hemostasis. In Orkin SH, Fisher DE, Ginsburg D, Look TA, Lux SE, Nathan DG Eds. Nathan and Oski’s Hematology and Oncology of Infancy and Childhood 8th Ed. Elsevier Saunders, Philadelphia. 2015:1103-24.]Search in Google Scholar
[23. Tiede A, Priesack J, Werwitzke S, Bohlmann K, Oortwijn B, Lenting P, et al. Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single centre cohort study. J Thromb Haemost. 2008;6(4):569-76. DOI: 10.1111/j.1538-7836.2008.02909.x10.1111/j.1538-7836.2008.02909.x18208537]Search in Google Scholar
[24. Manfredi E, van Zaane B, Gerdes V.E.A, Brandjes D.P.M, Squizzato A. Hypothyroidism and acquired von Willebrand’s syndrome: a systematic review. Haemophilia. 2008;14(3):423-33. DOI: 10.1111/j.1365-2516.2007.01642.x10.1111/j.1365-2516.2007.01642.x18218015]Search in Google Scholar
[25. Stuijver DJ, Piantanida E, van Zaane B, Galli L, Romualdi E, Tanda ML, et al. Acquired von Willebrand syndrome in patients with overt hypothyroidism: a prospective cohort study. Haemophilia. 2014;20(3):326-32. DOI: 10.1111/hae.1227510.1111/hae.1227524118466]Search in Google Scholar