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British Journal of Haematology|February 14, 2002
Axillary vein thrombosis in a healthy donor following platelet apheresisD A Jones, E Williams, S A Riley, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 2010
A family of diiron monooxygenases catalyzing amino acid beta-hydroxylation in antibiotic biosynthesisThomas M Makris, Mrinmoy Chakrabarti, Eckard Münck, et al.
International Journal of Laboratory Hematology|March 16, 2011
The phenotypic and genetic assessment of antithrombin deficiencyP C Cooper, F Coath, M E Daly, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 26, 2012
How I treat inhibitors in haemophiliaM Makris, C R M Hay, A Gringeri, et al.
British Journal of Haematology|October 23, 1997
Protein C and protein S in homozygous sickle cell disease: does hepatic dysfunction contribute to low levels?J G Wright, R Malia, P Cooper, et al.
Thrombosis and Haemostasis|September 24, 1999
A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutationsI M Nesbitt, K K Hampton, F E Preston, et al.
British Medical Journal|February 25, 1978
Cellular hyperviscosity as a cause of neurological symptoms in leukaemiaF E Preston, R J Sokol, J S Lilleyman, et al.
Lancet (London, England)|December 27, 1975
Platelet abnormalities in diabetic peripheral neuropathyC B O'Malley, J D Ward, W R Timperley, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 1, 1991
The effects of diet and insulin therapy on coagulation factor VII, blood viscosity, and platelet release proteins in diabetic patients with secondary sulphonylurea failureA M Jennings, I Ford, S Murdoch, et al.
British Journal of Haematology|June 1, 1997
The role of immunoglobulin G and fibrinogen in platelet aggregation by Streptococcus sanguisI Ford, C W Douglas, D Cox, et al.
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