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Blood|June 1, 1989
Partial gene deletion in a family with factor X deficiencyF Bernardi, G Marchetti, P Patracchini, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2004
Severe factor X deficiency in pregnancy: case report and review of the literatureC Romagnolo, S Burati, S Ciaffoni, et al.Thrombosis and Haemostasis|December 30, 1998
4G/5G polymorphism of PAI-1 gene promoter and fibrinolytic capacity in patients with deep vein thrombosisM T Sartori, B Wiman, S Vettore, et al.Thrombosis Research|June 1, 2000
Tissue factor pathway inhibitor levels in patients with homocystinuriaG Cella, A Burlina, A Sbarai, et al.Annals of Hematology|October 1, 1995
Different organization of von Willebrand factor oligomers in type-2A and -2B von Willebrand disease variants: effects of DDAVP infusion and protease inhibitorsA Casonato, E Pontara, A Bertomoro, et al.Acta Haematologica|January 1, 1994
Acquired factor VIII:C inhibitor in a patient with Sjögren's syndrome: successful treatment with steroid and immunosuppressive therapyD Dannhäuser, A Casonato, F Pietrogrande, et al.Journal of Animal Science|June 23, 2009
Effect of rearing system and of dietary protein level on leptin, growth, and carcass composition in young Podolian bullsR Marino, A Braghieri, M Albenzio, et al.Meat Science|November 9, 2011
Chemical, physical and sensory properties of meat from pure and crossbred Podolian bulls at different ageing timesA Braghieri, G F Cifuni, A Girolami, et al.Blood|April 1, 1996
Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domainT Izumi, T Hashiguchi, G Castaman, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1993
First report of combined factor VII Padua defect and von Willebrand's disease due to casual association of the two defectsA Girolami, E Pontara, D Dannhauser, et al.Pageof 59