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British Journal of Haematology|March 1, 1992
A patient with von Willebrand's disease characterized by a compound heterozygosity for a substitution of Arg854 by Gln in the putative factor-VIII-binding domain of von Willebrand factor (vWF) on one allele and very low levels of mRNA from the second vWF alleleK Peerlinck, J C Eikenboom, H K Ploos Van Amstel, et al.Haemostasis|January 1, 1987
Hip surgery in a patient with severe factor VII deficiencyE Briët, G OnvleeThrombosis and Haemostasis|July 1, 1995
Clinical trials of primary and secondary prevention of thrombosis and restenosisJ VermylenHaemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
How do some haemophiliacs develop inhibitors?J VermylenPathologie-Biologie|December 1, 1975
Physical and chemical properties of normal and haemophilic factor VIIIJ VermylenBlood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 1, 1995
Approaching the ideal: therapeutic requirements for factor VIII concentratesJ VermylenNederlands Tijdschrift Voor Geneeskunde|February 22, 2000
[Physical diagnosis--percussion and palpation of the spleen]M H Godfried, E BriëtNederlands Tijdschrift Voor Geneeskunde|March 22, 2000
[Blind spots of the diagnostic hemostasis screen]M Levi, M Peters, E BriëtNederlands Tijdschrift Voor Geneeskunde|April 29, 1998
[Revision consensus hemophilia: treatment and responsibility. Nederlandse Vereniging van Hemophilia Patients]E Briët, E P Mauser-BunschotenPageof 37