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Clinical and Laboratory Haematology|December 21, 2000
A survey of patients with acquired haemophilia in a haemophilia centre over a 28-year periodT T Yee, A Taher, K J Pasi, et al.BJU International|June 15, 1999
Thrombotic risk factors associated with transurethral prostatectomyC R Bell, P J Murdock, K J Pasi, et al.British Journal of Haematology|April 7, 1999
Factor VIII inhibitors in haemophiliacs: a single-centre experience over 34 years, 1964-97T T Yee, K J Pasi, P A Lilley, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three casesM S Enayat, B D Theophilus, K J Pasi, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 14, 2011
Access to primary dental care for patients with inherited bleeding disordersH Kalsi, L Nanayakkara, K J Pasi, et al.British Journal of Haematology|November 1, 1991
Consistently normal CD4+, CD8+ levels in haemophilic boys only treated with a virally safe factor VIII concentrate (BPL 8Y)J A Evans, K J Pasi, M D Williams, et al.British Journal of Haematology|May 1, 1996
Transmission of symptomatic parvovirus B19 infection by clotting factor concentrateT T Yee, B J Cohen, K J Pasi, et al.British Journal of Haematology|June 1, 1990
Clinical and laboratory evaluation of the treatment of von Willebrand's disease patients with heat-treated factor VIII concentrate (BPL 8Y)K J Pasi, M D Williams, M S Enayat, et al.Archives of Disease in Childhood|January 1, 1990
Growth in haemophilic boys after HIV infectionK J Pasi, M A Collins, A K Ewer, et al.British Journal of Haematology|September 1, 1995
Association of changes in monocyte antigen presentation and cytokine production in haemophilic boys with treatment and blood-borne virus infectionK J Pasi, J A Evans, M Wadhwa, et al.Pageof 6