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Thrombosis Research|May 1, 1982
Plasma 6-keto-prostaglandin F1alpha: fact or fictionM Greaves, F E PrestonSeminars in Thrombosis and Hemostasis|May 18, 1999
Alternative models of delivery of anticoagulant servicesM MakrisThrombosis and Haemostasis|January 10, 1998
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophiliaM Makris, F E Preston, N J Beauchamp, et al.Acta Haematologica|January 1, 1983
Haemorrhage and factor IX deficiency in pituitary insufficiencyB E Woodcock, F E PrestonBritish Medical Journal|June 8, 1974
The kidney and intravascular coagulation in myelomatosisA M Ward, F E PrestonBlood|March 9, 2000
Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein SM Makris, M Leach, N J Beauchamp, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 12, 2000
Monitoring unfractionated heparin therapy: relationship between eight anti-Xa assays and a protamine titration assayS Kitchen, J Theaker, F E PrestonEuropean Journal of Haematology|September 1, 1987
Potential value of vintristine-adriamycin-dexamethasone combination chemotherapy (VAD) in refractory and rapidly progressive myelomaR Collin, M Greaves, F E PrestonBlood|October 9, 1998
Antithrombins Wibble and Wobble (T85M/K): archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activationN J Beauchamp, R N Pike, M Daly, et al.Pageof 39