Effect kinetics of desmopressin‐induced platelet retention in healthy volunteers treated with aspirin or placebo
暂无分享,去创建一个
[1] I. Nilsson,et al. Association between factor VIII related antigen and plasminogen activator. , 2009, Acta medica Scandinavica.
[2] V. Kretschmer,et al. DDAVP'S Shortening of the Bleeding Time Seems Due to Plasma von Willebrand Factor , 1995, Seminars in Thrombosis & Hemostasis.
[3] M. Cattaneo,et al. Role of ADP in platelet aggregation at high shear: studies in a patient with congenital defect of platelet responses to ADP , 1994, British journal of haematology.
[4] J. Klimeš,et al. Simultaneous high-performance liquid chromatographic determination of salicylates in whole blood, plasma and isolated erythrocytes. , 1992, Journal of chromatography.
[5] S. Lethagen,et al. DDAVP‐induced enhancement of platelet retention: Its dependence on platelet‐von Willebrand Factor and the platelet receptor GP IIb/IIIa , 1992, European journal of haematology.
[6] S. Lethagen,et al. The Effect of DDAVP and Placebo on Platelet Function and Prolonged Bleeding Time Induced by Oral Acetyl Salicylic Acid Intake in Healthy Volunteers , 1992, Thrombosis and Haemostasis.
[7] T. Wüst,et al. Influence of different surfactants on the separation of von Willebrand factor multimers by use of agarose gel electrophoresis and semi dry blotting technology. , 1991, Thrombosis research.
[8] S. Lethagen,et al. Effects of desmopressin acetate (DDAVP) and dextran on hemostatic and thromboprophylactic mechanisms. , 1990, Acta chirurgica Scandinavica.
[9] G. Rock. A comparison of two methods for the discrimination of VWF:AG multimers. , 1990, Thrombosis research.
[10] W. Hathaway,et al. Use of DDAVP in inherited and acquired platelet dysfunction , 1990, American journal of hematology.
[11] Z. Zeigler. Platelet glass bead retention is useful in monitoring response to 1‐deamino‐8‐D‐arginine‐vasopressin (d‐DAVP) , 1989, American journal of hematology.
[12] E. Salzman,et al. Changes in von Willebrand factor during cardiac surgery: effect of desmopressin acetate. , 1988, Blood.
[13] J. White,et al. Shortening of Bleeding Time by 1-Deamino-8-Arginine Vasopressin (DDAVP) in the Absence of Platelet von Willebrand Factor in Gray Platelet Syndrome , 1987, Thrombosis and Haemostasis.
[14] E. Wenzel,et al. Comparative Study of Intranasal, Subcutaneous and Intravenous Administration of Desamino-D-Arginine Vasopressin (DDAVP) , 1986, Thrombosis and Haemostasis.
[15] J. Sixma,et al. DDAVP enhances platelet adherence and platelet aggregate growth on human artery subendothelium. , 1984, Blood.
[16] M. Cheang,et al. SHORTENING OF BLEEDING TIME BY 1-DEAMINO-8-D-ARGININE VASOPRESSIN IN VARIOUS BLEEDING DISORDERS , 1984, The Lancet.
[17] P. Mannucci,et al. Response of Factor VIII/von Willebrand Factor to DDAVP in Healthy Subjects and Patients with Haemophilia A and von Willebrand's Disease , 1981, British journal of haematology.
[18] R. Furlong,et al. Factor VIII and Fibrinolytic Response to Deamino‐8‐d‐Argenine Vasopressin in Normal Subjects and Dissociate Response in Some Patients with Haemophilia and von Willebrand's Disease , 1980 .
[19] M. Moia,et al. DDAVP shortens the prolonged bleeding times of patients with severe von Willebrand disease treated with cryoprecipitate. Evidence for a mechanism of action independent of released von Willebrand factor. , 1989, Blood.
[20] P. Mannucci,et al. Controlled trial of desmopressin in liver cirrhosis and other conditions associated with a prolonged bleeding time. , 1986, Blood.
[21] A. Federici,et al. Multimeric composition of factor VIII/von Willebrand factor following administration of DDAVP: implications for pathophysiology and therapy of von Willebrand's disease subtypes. , 1982, Blood.