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A R Giles

Showing results (11-20 of 72) with videos related to

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Thrombosis and Haemostasis|February 3, 1992
Normalization of the haemostatic plugs of dogs with haemophilia A (factor VIII deficiency) following the infusion of a combination of factor Xa and phosphatidylcholine/phosphatidylserine vesiclesN i Hong yu, A R Giles
British Journal of Haematology|November 1, 1987
Type IIB von Willebrand's disease presenting as thrombocytopenia during pregnancyA R Giles, H Hoogendoorn, K Benford
Blood|September 1, 1982
A canine model of hemophilic (factor VIII:C deficiency) bleedingA R Giles, S Tinlin, R Greenwood
British Journal of Haematology|May 1, 1984
A platelet release defect induced by aspirin or penicillin G does not increase gastrointestinal blood loss in thrombocytopenic rabbitsA R Giles, P Greenwood, S Tinlin
Thrombosis Research|June 15, 1984
The thrombogenicity of prothrombin complex concentrates. IV. The source of coagulant-active phospholipidA R Giles, H Hoogendoorn, S Tinlin
Thrombosis and Haemostasis|January 11, 1993
The development of homologous (canine/anti-canine) antibodies in dogs with haemophilia A (factor VIII deficiency): a ten-year longitudinal studyS Tinlin, S Webster, A R Giles
Thrombosis Research|February 1, 1981
The thrombogenicity of prothrombin complex concentrates: III. The relationship of in vivo thrombogenicity to the nature of the starting plasmaA R Giles, H Hoogendoorn, M A Blajchman
Blood|June 1, 1990
A qualitative and quantitative analysis of the activation and inactivation of protein C in vivo in a primate modelH Hoogendoorn, M E Nesheim, A R Giles
British Journal of Haematology|December 1, 1993
The generation of thrombin in vivo induces the selective loss of high molecular weight multimers of von Willebrand factor and the reversible sequestration of plateletsC H Toh, H Hoogendoorn, A R Giles
American Journal of Human Genetics|January 1, 1992
Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand diseaseE W Murray, A R Giles, D Lillicrap
Pageof 8

Showing results (11-20 of 72) with videos related to

Sort By:
Pageof 8
Thrombosis and Haemostasis|February 3, 1992
Normalization of the haemostatic plugs of dogs with haemophilia A (factor VIII deficiency) following the infusion of a combination of factor Xa and phosphatidylcholine/phosphatidylserine vesiclesN i Hong yu, A R Giles
British Journal of Haematology|November 1, 1987
Type IIB von Willebrand's disease presenting as thrombocytopenia during pregnancyA R Giles, H Hoogendoorn, K Benford
Blood|September 1, 1982
A canine model of hemophilic (factor VIII:C deficiency) bleedingA R Giles, S Tinlin, R Greenwood
British Journal of Haematology|May 1, 1984
A platelet release defect induced by aspirin or penicillin G does not increase gastrointestinal blood loss in thrombocytopenic rabbitsA R Giles, P Greenwood, S Tinlin
Thrombosis Research|June 15, 1984
The thrombogenicity of prothrombin complex concentrates. IV. The source of coagulant-active phospholipidA R Giles, H Hoogendoorn, S Tinlin
Thrombosis and Haemostasis|January 11, 1993
The development of homologous (canine/anti-canine) antibodies in dogs with haemophilia A (factor VIII deficiency): a ten-year longitudinal studyS Tinlin, S Webster, A R Giles
Thrombosis Research|February 1, 1981
The thrombogenicity of prothrombin complex concentrates: III. The relationship of in vivo thrombogenicity to the nature of the starting plasmaA R Giles, H Hoogendoorn, M A Blajchman
Blood|June 1, 1990
A qualitative and quantitative analysis of the activation and inactivation of protein C in vivo in a primate modelH Hoogendoorn, M E Nesheim, A R Giles
British Journal of Haematology|December 1, 1993
The generation of thrombin in vivo induces the selective loss of high molecular weight multimers of von Willebrand factor and the reversible sequestration of plateletsC H Toh, H Hoogendoorn, A R Giles
American Journal of Human Genetics|January 1, 1992
Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand diseaseE W Murray, A R Giles, D Lillicrap
Pageof 8