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British Journal of Haematology|July 1, 1995
Development of resistance to activated protein C during pregnancyA M Cumming, R C Tait, S Fildes, et al.British Journal of Haematology|August 1, 1997
The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic populationA M Cumming, S Keeney, A Salden, et al.The Quarterly Journal of Medicine|January 1, 1982
Familial antithrombin III deficiencyJ H Winter, A Fenech, W Ridley, et al.British Journal of Haematology|June 1, 1990
Clinical and laboratory evaluation of National Health Service factor VIII concentrate (8Y) for the treatment of von Willebrand's diseaseA M Cumming, S Fildes, I R Cumming, et al.Kidney International|January 1, 1981
Assessment of total and divided renal plasma flow by 123I-hippuran renographyA Mackay, A S Eadie, A M Cumming, et al.Scandinavian Journal of Haematology|January 1, 1984
A search for the mechanism underlying the altered MCV in thyroid dysfunction: a study of serum and red cell membrane lipidsR J Davidson, A M Cumming, V H Leel, et al.Postgraduate Medical Journal|July 1, 1980
Severe hypokalaemia with paralysis induced by small doses of liquoriceA M Cumming, K Boddy, J J Brown, et al.Acta Endocrinologica|July 1, 1983
Primary hyperparathyroidism associated with primary hyperaldosteronismJ B Ferriss, J J Brown, A M Cumming, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|July 16, 2009
The mutation spectrum associated with type 3 von Willebrand disease in a cohort of patients from the north west of EnglandM S Sutherland, S Keeney, P H B Bolton-Maggs, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 17, 2017
Evaluation of the use of rotational thromboelastometry in the assessment of FXI deficencyG N Pike, A M Cumming, J Thachil, et al.Pageof 8