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2. von Willebrand's disease. Pathogenesis and clinical aspects. Lethagen S Crit Rev Oncol Hematol; 1993 Aug; 15(1):1-11. PubMed ID: 8240703 [No Abstract] [Full Text] [Related]
3. [Variant forms of von Willebrand's disease]. Papaian LP; Golovina OG Ter Arkh; 1990; 62(7):86-92. PubMed ID: 2251672 [TBL] [Abstract][Full Text] [Related]
4. von Willebrand factor and platelet function. Moroose R; Hoyer LW Annu Rev Med; 1986; 37():157-63. PubMed ID: 2939788 [TBL] [Abstract][Full Text] [Related]
5. [Inborn and acquired von Willebrand disease]. Schneppenheim R; Barthels M; Budde U Hamostaseologie; 2005 Nov; 25(4):367-75. PubMed ID: 16395486 [TBL] [Abstract][Full Text] [Related]
6. [Inborn and acquired von Willebrand disease]. Schneppenheim R; Budde U Hamostaseologie; 2008 Dec; 28(5):312-9. PubMed ID: 19132162 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Von Willebrand disease: from diagnosis to treatment]. Fressinaud E; Meyer D Rev Prat; 2005 Dec; 55(20):2209-18. PubMed ID: 16519045 [TBL] [Abstract][Full Text] [Related]
9. Advances in the diagnosis and management of von Willebrand disease. Franchini M Hematology; 2006 Aug; 11(4):219-25. PubMed ID: 17178659 [TBL] [Abstract][Full Text] [Related]
10. Characterization of recessive severe type 1 and 3 von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related von Willebrand factor deficiency, and dominant type 1 VWD. Michiels JJ; Berneman Z; Gadisseur A; van der Planken M; Schroyens W; van de Velde A; van Vliet H Clin Appl Thromb Hemost; 2006 Jul; 12(3):277-95. PubMed ID: 16959681 [TBL] [Abstract][Full Text] [Related]
11. Laboratory diagnosis and molecular basis of mild von Willebrand disease type 1. Michiels JJ; Berneman Z; Gadisseur A; van der Planken M; Schroyens W; van Vliet HH Acta Haematol; 2009; 121(2-3):85-97. PubMed ID: 19506353 [TBL] [Abstract][Full Text] [Related]
12. Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families. Castaman G; Giacomelli S; Rodeghiero F Acta Haematol; 2009; 121(2-3):106-10. PubMed ID: 19506356 [TBL] [Abstract][Full Text] [Related]
13. Von Willebrand's disease. Clinical picture, diagnosis, and treatment. Bowie EJ Clin Lab Med; 1984 Jun; 4(2):303-17. PubMed ID: 6209061 [TBL] [Abstract][Full Text] [Related]
14. Management of inherited von Willebrand disease in 2007. Federici AB; Mannucci PM Ann Med; 2007; 39(5):346-58. PubMed ID: 17701477 [TBL] [Abstract][Full Text] [Related]
15. Laboratory and molecular characteristics of recessive von Willebrand disease type 2C (2A subtype IIC) of variable severity due to homozygous or double heterozygous mutations in the D1 and D2 domains. Michiels JJ; Gadisseur A; van der Planken M; Schroyens W; Berneman Z Acta Haematol; 2009; 121(2-3):111-8. PubMed ID: 19506357 [TBL] [Abstract][Full Text] [Related]
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17. [Hemostatic effect of deamino-8-D-arginine vasopressin (DDAVP) in hemophilia A and von Willebrand's disease]. Fukui H; Takase T Rinsho Ketsueki; 1985 Jul; 26(7):1069-79. PubMed ID: 3932720 [No Abstract] [Full Text] [Related]