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The Journal of Laboratory and Clinical Medicine|April 1, 1990
Factor IXa and von Willebrand factor modify the inactivation of factor VIII by activated protein CM E Rick, N L Esmon, D M KrizekBritish Journal of Haematology|October 1, 1987
Interleukin 1 or endotoxin increases the release of von Willebrand factor from human endothelial cellsA E Schorer, C F Moldow, M E RickArchives of Internal Medicine|November 1, 1981
Studies on a circulating anticoagulant in procainamide-induced lupus erythematosusR L Edwards, M E Rick, C J WakemSpine|November 29, 2001
Transfusion medicine management for reconstructive spinal repair in a patient with von Willebrand's disease and a history of heavy surgical bleedingC D Bolan, M E Rick, D W PollyProceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Role of carbohydrate in multimeric structure of factor VIII/von Willebrand factor proteinH R Gralnick, S B Williams, M E RickInvestigative Ophthalmology & Visual Science|June 1, 1988
Plasma fibrinopeptide A, beta-thromboglobulin, and platelet factor 4 in diabetic retinopathyM S Roy, M J Podgor, M E RickThe Journal of Clinical Investigation|June 1, 1973
Tissue factor activity in lymphocyte cultures from normal individuals and patients with hemophilia AF R Rickles, J A Hardin, F A Pitlick, et al.American Journal of Human Genetics|March 1, 1997
Partial correction of a severe molecular defect in hemophilia A, because of errors during expression of the factor VIII geneM Young, H Inaba, L W Hoyer, et al.Blood|June 1, 1985
Prenatal diagnosis of classic hemophilia (hemophilia A) by immunoradiometric assaysL W Hoyer, C A Carta, M S Golbus, et al.The American Journal of Medicine|March 1, 1977
von Willebrand's disease and hemorrhagic telangiectasia: association of two complex disorders of hemostasis resulting in life-threatening hemorrhageD J Ahr, F R Rickles, L W Hoyer, et al.Pageof 12