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Journal of Clinical Pathology|October 1, 1993
Role of beta 2-glycoprotein I and anti-phospholipid antibodies in activation of protein C in vitroD M Keeling, A J Wilson, I J Mackie, et al.Archives of Disease in Childhood|December 13, 2003
Brain haemorrhage in five infants with coagulopathyE B A Vorstman, P Anslow, D M Keeling, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 14, 2011
Management of muscle haematomas in patients with severe haemophilia in an evidence-poor worldB Sørensen, G M Benson, M Bladen, et al.Leukemia|April 1, 1990
Sezary cell-like leukemia: a distinct type of mature T cell malignancyE Matutes, D M Keeling, A C Newland, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 13, 2010
Treatment related factors and inhibitor development in children with severe haemophilia AP S Maclean, M Richards, M Williams, et al.Journal of Thrombosis and Haemostasis : JTH|June 29, 2004
The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99S C Darby, D M Keeling, R J D Spooner, et al.Thrombosis and Haemostasis|April 20, 2001
Genetic predisposition to bleeding during oral anticoagulant therapy: evidence for common founder mutations (FIXVal-10 and FIXThr-10) and an independent CpG hotspot mutation (FIXThr-10)J Oldenburg, K Kriz, W A Wuillemin, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 15, 2010
Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophiliaA Peden, L McCardle, M W Head, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 17, 2004
Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' OrganizationK J Pasi, P W Collins, D M Keeling, et al.Pageof 3