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2. Acquired von Willebrand syndromes: clinical features, aetiology, pathophysiology, classification and management. Michiels JJ; Budde U; van der Planken M; van Vliet HH; Schroyens W; Berneman Z Best Pract Res Clin Haematol; 2001 Jun; 14(2):401-36. PubMed ID: 11686107 [TBL] [Abstract][Full Text] [Related]
3. [Acquired von Willebrand syndrome with autoimmune hemolytic anemia]. Sakai M; Shima M; Izumi Y; Shirahata A Rinsho Ketsueki; 2004 Mar; 45(3):223-7. PubMed ID: 15103936 [TBL] [Abstract][Full Text] [Related]
4. Response of von Willebrand factor parameters to desmopressin in patients with type 1 and type 2 congenital von Willebrand disease: diagnostic and therapeutic implications. Michiels JJ; van de Velde A; van Vliet HH; van der Planken M; Schroyens W; Berneman Z Semin Thromb Hemost; 2002 Apr; 28(2):111-32. PubMed ID: 11992235 [TBL] [Abstract][Full Text] [Related]
5. Intravenous DDAVP and factor VIII-von Willebrand factor concentrate for the treatment and prophylaxis of bleedings in patients With von Willebrand disease type 1, 2 and 3. Michiels JJ; van Vliet HH; Berneman Z; Gadisseur A; van der Planken M; Schroyens W; van der Velden A; Budde U Clin Appl Thromb Hemost; 2007 Jan; 13(1):14-34. PubMed ID: 17164493 [TBL] [Abstract][Full Text] [Related]
6. [IgA RIPA inhibitor in a case of acquired von Willebrand syndrome]. Takai Y; Koya H; Himei S; Hayashi H Rinsho Ketsueki; 1989 Dec; 30(12):2183-8. PubMed ID: 2621801 [TBL] [Abstract][Full Text] [Related]
7. Characterization, classification, and treatment of von Willebrand diseases: a critical appraisal of the literature and personal experiences. Michiels JJ; Gadisseur A; Budde U; Berneman Z; van der Planken M; Schroyens W; van de Velde A; van Vliet H Semin Thromb Hemost; 2005 Nov; 31(5):577-601. PubMed ID: 16276467 [TBL] [Abstract][Full Text] [Related]
8. Classification and characterization of hereditary types 2A, 2B, 2C, 2D, 2E, 2M, 2N, and 2U (unclassifiable) von Willebrand disease. Michiels JJ; Berneman Z; Gadisseur A; van der Planken M; Schroyens W; van de Velde A; van Vliet H Clin Appl Thromb Hemost; 2006 Oct; 12(4):397-420. PubMed ID: 17000885 [TBL] [Abstract][Full Text] [Related]
10. Von Willebrand's disease with spontaneous platelet aggregation induced by an abnormal plasma von Willebrand factor. Grainick HR; Williams SB; McKeown LP; Rick ME; Maisonneuve P; Jenneau C; Sultan Y J Clin Invest; 1985 Oct; 76(4):1522-9. PubMed ID: 2932469 [TBL] [Abstract][Full Text] [Related]
11. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio. Gadisseur A; Berneman Z; Schroyens W; Michiels JJ Acta Haematol; 2009; 121(2-3):128-38. PubMed ID: 19506359 [TBL] [Abstract][Full Text] [Related]
12. A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. Shen MC; Lin JS; Lin DS; Hsu SC; Lin B Thromb Res; 2003; 112(5-6):291-5. PubMed ID: 15041272 [TBL] [Abstract][Full Text] [Related]
13. Guidelines for the evaluation of intravenous desmopressin and von Willebrand factor/factor VIII concentrate in the treatment and prophylaxis of bleedings in von Willebrand disease types 1, 2, and 3. Michiels JJ; Gadisseur A; van der Planken M; Schroyens W; van de Velden A; Berneman Z Semin Thromb Hemost; 2006 Sep; 32(6):636-45. PubMed ID: 16977574 [TBL] [Abstract][Full Text] [Related]
14. Association of acquired von Willebrand syndrome with AL amyloidosis. Kos CA; Ward JE; Malek K; Sanchorawala V; Wright DG; O'Hara C; Connors L; Skinner M; Seldin DC Am J Hematol; 2007 May; 82(5):363-7. PubMed ID: 17205535 [TBL] [Abstract][Full Text] [Related]
15. Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF (High Purity)] in people with von Willebrand disorder. A randomised cross-over, multi-centre study. Favaloro EJ; Lloyd J; Rowell J; Baker R; Rickard K; Kershaw G; Street A; Scarff K; Barrese G; Maher D; McLachlan AJ Thromb Haemost; 2007 Jun; 97(6):922-30. PubMed ID: 17549293 [TBL] [Abstract][Full Text] [Related]
16. Plasma collagen cofactor correlates with von Willebrand factor antigen and ristocetin cofactor but not with bleeding time. Aihara M; Kimura A; Chiba Y; Yoshida Y Thromb Haemost; 1988 Jun; 59(3):485-90. PubMed ID: 3142084 [TBL] [Abstract][Full Text] [Related]
17. Dominant von Willebrand disease type 2M and 2U are variable expressions of one distinct disease entity caused by loss-of-function mutations in the A1 domain of the von Willebrand factor gene. Gadisseur A; van der Planken M; Schroyens W; Berneman Z; Michiels JJ Acta Haematol; 2009; 121(2-3):145-53. PubMed ID: 19506361 [TBL] [Abstract][Full Text] [Related]
18. Non-surgical bleeding in patients with ventricular assist devices could be explained by acquired von Willebrand disease. Geisen U; Heilmann C; Beyersdorf F; Benk C; Berchtold-Herz M; Schlensak C; Budde U; Zieger B Eur J Cardiothorac Surg; 2008 Apr; 33(4):679-84. PubMed ID: 18282712 [TBL] [Abstract][Full Text] [Related]
19. Laboratory testing for von Willebrand disease: contribution of multimer analysis to diagnosis and classification. Budde U; Pieconka A; Will K; Schneppenheim R Semin Thromb Hemost; 2006 Jul; 32(5):514-21. PubMed ID: 16862525 [TBL] [Abstract][Full Text] [Related]
20. Three cases of acquired von Willebrand disease associated with systemic lupus erythematosus. Viallard JF; Pellegrin JL; Vergnes C; Borel-Derlon A; Clofent-Sanchez G; Nurden AT; Leng B; Nurden P Br J Haematol; 1999 May; 105(2):532-7. PubMed ID: 10233433 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]