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Journal of Thrombosis and Haemostasis : JTH|October 26, 2005
Attitudes toward genetic testing for thrombophilia in asymptomatic members of a large family with heritable protein C deficiencyI M van Korlaar, C Y Vossen, F R Rosendaal, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1992
Exploration of rapid bedside monitoring of coagulation and fibrinolysis parameters during thrombolytic therapyD C Sane, N J Gresalfi, L A Enney-O'Mara, et al.
International Journal of Radiation Oncology, Biology, Physics|August 1, 1983
Desmoid tumors: local control and patterns of relapse following radiation therapyS A Leibel, W M Wara, D R Hill, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 23, 2002
Characterization of the human prostaglandin H synthase 1 gene (PTGS1): exclusion by genetic linkage analysis as a second modifier gene in familial thrombosisB T Scott, S J Hasstedt, E G Bovill, et al.
Journal of Thrombosis and Haemostasis : JTH|June 28, 2005
Chronic venous abnormalities in symptomatic and asymptomatic protein C deficiencyJ Emmerich, C Y Vossen, P W Callas, et al.
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