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Acquired von Willebrand syndrome: from pathophysiology to management.
Veyradier A, Jenkins CS, Fressinaud E, Meyer D. Veyradier A, et al. Thromb Haemost. 2000 Aug;84(2):175-82. Thromb Haemost. 2000. PMID: 10959686 Review. No abstract available.
Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor.
Sadler JE, Budde U, Eikenboom JC, Favaloro EJ, Hill FG, Holmberg L, Ingerslev J, Lee CA, Lillicrap D, Mannucci PM, Mazurier C, Meyer D, Nichols WL, Nishino M, Peake IR, Rodeghiero F, Schneppenheim R, Ruggeri ZM, Srivastava A, Montgomery RR, Federici AB; Working Party on von Willebrand Disease Classification. Sadler JE, et al. J Thromb Haemost. 2006 Oct;4(10):2103-14. doi: 10.1111/j.1538-7836.2006.02146.x. Epub 2006 Aug 2. J Thromb Haemost. 2006. PMID: 16889557 Review.
Improvement of von Willebrand factor proteolysis after prostacyclin infusion in severe pulmonary arterial hypertension.
Veyradier A, Nishikubo T, Humbert M, Wolf M, Sitbon O, Simonneau G, Girma JP, Meyer D. Veyradier A, et al. Circulation. 2000 Nov 14;102(20):2460-2. doi: 10.1161/01.cir.102.20.2460. Circulation. 2000. PMID: 11076816 Clinical Trial.
Therapeutic monitoring of von Willebrand disease: interest and limits of a platelet function analyser at high shear rates.
Fressinaud E, Veyradier A, Sigaud M, Boyer-Neumann C, Le Boterff C, Meyer D. Fressinaud E, et al. Br J Haematol. 1999 Sep;106(3):777-83. doi: 10.1046/j.1365-2141.1999.01604.x. Br J Haematol. 1999. PMID: 10468873
Conformational changes in the D' domain of von Willebrand factor induced by CYS 25 and CYS 95 mutations lead to factor VIII binding defect and multimeric impairment.
Jorieux S, Fressinaud E, Goudemand J, Gaucher C, Meyer D, Mazurier C. Jorieux S, et al. Blood. 2000 May 15;95(10):3139-45. Blood. 2000. PMID: 10807780
Moreover, the use of anti-vWF monoclonal antibodies that inhibit the FVIII binding showed that these 2 mutations likely induce a conformational change in the D' domain. These results show that the native conformation of the D' domain of vWF is not only required for …
Moreover, the use of anti-vWF monoclonal antibodies that inhibit the FVIII binding showed that these 2 mutations likely induce a conformatio …
Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD).
Budde U, Schneppenheim R, Eikenboom J, Goodeve A, Will K, Drewke E, Castaman G, Rodeghiero F, Federici AB, Batlle J, Pérez A, Meyer D, Mazurier C, Goudemand J, Ingerslev J, Habart D, Vorlova Z, Holmberg L, Lethagen S, Pasi J, Hill F, Peake I. Budde U, et al. J Thromb Haemost. 2008 May;6(5):762-71. doi: 10.1111/j.1538-7836.2008.02945.x. Epub 2008 Mar 1. J Thromb Haemost. 2008. PMID: 18315556 Clinical Trial.
Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD.
Eikenboom J, Van Marion V, Putter H, Goodeve A, Rodeghiero F, Castaman G, Federici AB, Batlle J, Meyer D, Mazurier C, Goudemand J, Schneppenheim R, Budde U, Ingerslev J, Vorlova Z, Habart D, Holmberg L, Lethagen S, Pasi J, Hill F, Peake I. Eikenboom J, et al. J Thromb Haemost. 2006 Apr;4(4):774-82. doi: 10.1111/j.1538-7836.2006.01823.x. J Thromb Haemost. 2006. PMID: 16634746
Acquired von Willebrand syndrome: data from an international registry.
Federici AB, Rand JH, Bucciarelli P, Budde U, van Genderen PJ, Mohri H, Meyer D, Rodeghiero F, Sadler JE; Subcommittee on von Willebrand Factor. Federici AB, et al. Thromb Haemost. 2000 Aug;84(2):345-9. Thromb Haemost. 2000. PMID: 10959711
[Biological diagnosis of Willebrand disease].
Siguret V, Ribba AS, Meyer D. Siguret V, et al. Ann Biol Clin (Paris). 1997 Nov-Dec;55(6):601-6. Ann Biol Clin (Paris). 1997. PMID: 9499922 French. No abstract available.
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