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Haemophilia : the Official Journal of the World Federation of Hemophilia|February 5, 2016
Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand diseaseS M Siboni, E Biguzzi, V Caiani, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 3, 2004
Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and ItalyM Karimi, F Peyvandi, S Siboni, 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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 24, 2017
A comparative evaluation of a new fully automated assay for von Willebrand factor collagen binding activity to an established methodF Stufano, L Baronciani, D Mane-Padros, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 14, 2013
A two-centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigenF Stufano, A S Lawrie, S La Marca, et al.
International Journal of Laboratory Hematology|August 3, 2017
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratoriesI Jennings, S Kitchen, M Menegatti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiencyF Peyvandi, P M Mannucci, D Asti, et al.
International Journal of Laboratory Hematology|April 14, 2017
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratoriesI Jennings, S Kitchen, M Menegatti, et al.
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