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The American Journal of Medicine|August 1, 1980
Acquired dysfunction due to the circulation of "exhausted" plateletsF I Pareti, A Capitanio, L Mannucci, et al.British Journal of Haematology|March 1, 1982
Treatment of congenital antithrombin III deficiency with concentratesP M Mannucci, C Boyer, M Wolf, et al.Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|November 12, 2014
[Patient selection as the key to success of metabolic surgery]M Colombo-BenkmannAmerican Journal of Hematology|March 1, 1992
Human parvovirus B19 infection in hemophiliacs first infused with two high-purity, virally attenuated factor VIII concentratesA Azzi, S Ciappi, K Zakvrzewska, et al.British Journal of Haematology|April 8, 1998
Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIIIF Peyvandi, E G Tuddenham, A M Akhtari, et al.British Journal of Haematology|November 1, 1982
Significance of plasma fibrinopeptide A and high molecular weight fibrinogen in patients with liver cirrhosisS Coccheri, P M Mannucci, G Palareti, et al.Journal of Thrombosis and Haemostasis : JTH|December 13, 2006
Biochemical characterization of a recombinant von Willebrand factor (VWF) with combined type 2B and type 1 defects in the VWF gene in two patients with a type 2A phenotype of von Willebrand diseaseL Baronciani, A B Federici, G Cozzi, et al.American Journal of Hematology|May 1, 1987
Correction of the bleeding time in treated patients with severe von Willebrand disease is not solely dependent on the normal multimeric structure of plasma von Willebrand factorP M Mannucci, M Moia, P Rebulla, et al.Thrombosis and Haemostasis|February 1, 1993
The genetic defect of type I von Willebrand disease "Vicenza" is linked to the von Willebrand factor geneA M Randi, E Sacchi, G C Castaman, et al.European Journal of Internal Medicine|June 17, 2018
Implementation of the Frailty Index in hospitalized older patients: Results from the REPOSI registerM Cesari, C Franchi, L Cortesi, et al.Pageof 115