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American Journal of Hematology|January 1, 1996
Abnormally large von Willebrand factor multimers in Henoch-Schönlein purpuraA Casonato, E Pontara, A Bertomoro, et al.Thrombosis and Haemostasis|November 1, 2001
Abnormal propeptide processing resulting in the presence of two abnormal species of protein C in plasma: characterization of the dysfunctional protein C Padua3 (protein C(R-1L/propeptide))P Simioni, M Kalafatis, D Tormene, et al.Blood|August 15, 2000
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic familyE Castoldi, P Simioni, M Kalafatis, et al.British Journal of Haematology|March 12, 2002
Lack of multimer organization of von Willebrand factor in an acquired von Willebrand syndromeA Casonato, E Pontara, A Doria, et al.Thrombosis and Haemostasis|September 1, 1993
Comparison of real-time B-mode ultrasonography and Doppler ultrasound with contrast venography in the diagnosis of venous thrombosis in symptomatic outpatientsA Cogo, A W Lensing, P Prandoni, et al.Thrombosis Research|April 15, 1997
Accuracy of two newly described D-dimer tests in patients with suspected deep venous thrombosisL Scarano, E Bernardi, P Prandoni, et al.Haematologia|January 1, 1993
Pyoderma gangrenosum associated with idiopathic myelofibrosis. Case historyD Sgarabotto, F Vianello, P Valeri, et al.Journal of Thrombosis and Haemostasis : JTH|December 5, 2012
Platelets express and release osteocalcin and co-localize in human calcified atherosclerotic plaquesC Foresta, G Strapazzon, L De Toni, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 1, 1996
DDAVP infusion in haemophilia A carriers: different behaviour of plasma factor VIII and von Willebrand factorA Casonato, D Dannhauser, E Pontara, et al.Transplantation|February 12, 1998
Impairment of fibrinolytic potential in long-term steroid treatment after heart transplantationG M Patrassi, M T Sartori, U Livi, et al.Pageof 59