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6. Laboratory monitoring of therapy in von Willebrand disease: efficacy of the PFA-100 and von Willebrand factor:collagen-binding activity as coupled strategies. Favaloro EJ Semin Thromb Hemost; 2006 Sep; 32(6):566-76. PubMed ID: 16977567 [TBL] [Abstract][Full Text] [Related]
7. [Von Willebrand disease: a common and unrecognized bleeding disorder]. Boehlen F; Robert-Ebadi H; de Moerloose P Rev Med Suisse; 2007 Feb; 3(97):346-50. PubMed ID: 17370733 [TBL] [Abstract][Full Text] [Related]
8. Diagnosis and treatment of von Willebrand disease. Cox Gill J Hematol Oncol Clin North Am; 2004 Dec; 18(6):1277-99, viii. PubMed ID: 15511616 [TBL] [Abstract][Full Text] [Related]
9. [Acquired von Willebrand syndrome]. Sucker C; Stockschläder M; Zotz RB; Scharf RE Dtsch Med Wochenschr; 2004 Jul; 129(28-29):1581-5. PubMed ID: 15243910 [No Abstract] [Full Text] [Related]
10. Reassessment of the correlation between the von Willebrand Factor activity, the PFA-100, and the bleeding time in patients with von Willebrand disease. Nitu-Whalley IC; Lee CA; Hermans C Thromb Haemost; 2001 Aug; 86(2):715-6. PubMed ID: 11522030 [No Abstract] [Full Text] [Related]
11. High-dose intravenous immunoglobulin delays clearance of von Willebrand factor in acquired von Willebrand disease. van Genderen PJ; Terpstra W; Michiels JJ; Kapteijn L; van Vliet HH Thromb Haemost; 1995 May; 73(5):891-2. PubMed ID: 7482422 [No Abstract] [Full Text] [Related]
12. 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]
13. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology. Eikenboom JC Best Pract Res Clin Haematol; 2001 Jun; 14(2):365-79. PubMed ID: 11686105 [TBL] [Abstract][Full Text] [Related]
14. [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]
15. Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: a question of 2B or not 2B? A story of nonidentical twins? Or two sides of a multidenominational or multifaceted primary-hemostasis coin? Favaloro EJ Semin Thromb Hemost; 2008 Feb; 34(1):113-27. PubMed ID: 18393148 [TBL] [Abstract][Full Text] [Related]
16. Clinical, laboratory and therapeutic aspects of platelet-type von Willebrand disease. Franchini M; Montagnana M; Lippi G Int J Lab Hematol; 2008 Apr; 30(2):91-4. PubMed ID: 18333841 [TBL] [Abstract][Full Text] [Related]
17. Causes, etiology and diagnosis of acquired von Willebrand disease: a prospective diagnostic workup to establish the most effective therapeutic strategies. Sucker C; Michiels JJ; Zotz RB Acta Haematol; 2009; 121(2-3):177-82. PubMed ID: 19506364 [TBL] [Abstract][Full Text] [Related]
18. Immune tolerance induction with highly purified plasma-derived factor VIII containing von Willebrand factor in hemophilia A patients with high-responding inhibitors. Orsini F; Rotschild C; Beurrier P; Faradji A; Goudemand J; Polack B Haematologica; 2005 Sep; 90(9):1288-90. PubMed ID: 16154861 [TBL] [Abstract][Full Text] [Related]
19. Restoration of plasma von Willebrand factor deficiency is sufficient to correct thrombus formation after gene therapy for severe von Willebrand disease. De Meyer SF; Vandeputte N; Pareyn I; Petrus I; Lenting PJ; Chuah MK; VandenDriessche T; Deckmyn H; Vanhoorelbeke K Arterioscler Thromb Vasc Biol; 2008 Sep; 28(9):1621-6. PubMed ID: 18556568 [TBL] [Abstract][Full Text] [Related]
20. Management of inherited von Willebrand disease. Mannucci PM; Federici AB Best Pract Res Clin Haematol; 2001 Jun; 14(2):455-62. PubMed ID: 11686109 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]