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Arteriosclerosis, Thrombosis, and Vascular Biology|February 12, 1999
Study of the prothrombin gene 20201 GA variant in FV:Q506 carriers in relationship to the presence or absence of juvenile venous thromboembolismS Ehrenforth, M von Depka Prondsinski, E Aygören-Pürsün, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 13, 1998
Factor V Leiden and genetic defects of thrombophilia in childhood porencephalyO Debus, H G Koch, G Kurlemann, et al.
The Journal of Pediatrics|December 5, 1997
Factor V Leiden, protein C, and lipoprotein (a) in catheter-related thrombosis in childhood: a prospective studyU Nowak-Göttl, A Dübbers, D Kececioglu, et al.
European Journal of Haematology|January 1, 1996
Inhibition of hypercoagulation by antithrombin substitution in E. coli L-asparaginase-treated childrenU Nowak-Göttl, N Kuhn, J E Wolff, et al.
European Journal of Pediatrics|August 1, 1998
Cerebral venous sinus thrombosis in infancy and childhood: role of genetic and acquired risk factors of thrombophiliaH Vielhaber, S Ehrenforth, H G Koch, et al.
Thrombosis and Haemostasis|October 6, 1997
Arg506 to Gln mutation in the factor V gene causes poor fibrinolytic response in children after venous occlusionU Nowak-Göttl, M Binder, A Dübbers, et al.
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