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Journal of Inherited Metabolic Disease|January 1, 1981
Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twinsR G Gray, A D Patrick, F E Preston, et al.British Journal of Haematology|September 1, 1996
Evidence for the involvement of complement proteins in platelet aggregation by Streptococcus sanguis NCTC 7863I Ford, C W Douglas, J Heath, et al.British Journal of Haematology|January 1, 1989
Plasma D-dimer levels and their relationship to serum fibrinogen/fibrin degradation products in hypercoagulable statesJ T Wilde, S Kitchen, S Kinsey, et al.British Journal of Haematology|December 1, 1978
Characterization of serum fibrinogen and fibrin fragments produced during disseminated intravascular coagulationD A Lane, F E Preston, M E VanRoss, et al.Journal of Clinical Pathology|February 1, 1973
Intravascular coagulation and E. coli septicaemiaF E Preston, R G Malia, M J Sworn, et al.Postgraduate Medical Journal|October 1, 1988
Severe disseminated intravascular coagulation associated with massive ventricular mural thrombus following acute myocardial infarctionS A Solomon, D W Cotton, F E Preston, et al.British Journal of Haematology|April 1, 1995
The incidence of factor VIII inhibitors in the United Kingdom, 1990-93. Inhibitor Working Party. United Kingdom Haemophilia Centre Directors OrganizationB T Colvin, C R Hay, F G Hill, et al.Gut|January 1, 1978
Relationship between splenic size and splenic functionR C Smart, F P Ryan, C D Holdworth, et al.Thrombosis Et Diathesis Haemorrhagica|November 15, 1975
Serial changes in the coagulation system following clotting factor concentrate infusionF E Preston, D A Winfield, R G Malia, et al.Lancet (London, England)|June 29, 1985
Progressive liver disease in haemophilia: an understated problem?C R Hay, F E Preston, D R Triger, et al.Pageof 39