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A Casonato

Showing results (31-40 of 115) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|June 30, 2009
Uneventful coronary artery bypass surgery without prophylactic replacement therapy in a patient with a novel heterozygous FVII gene deletionL Gallinaro, A Casonato, F Vianello, et al.
Minerva Medica|May 26, 1980
[Juvenile rheumatoid arthritis appearing after hepatitis. Causal or casual relationship]G Amadori, A Milano, F Adami, et al.
Thrombosis and Haemostasis|July 10, 1998
On the release of von Willebrand factor from endothelial cells after venous occlusionA Casonato, E Pontara, A Bertomoro, et al.
Journal of Thrombosis and Thrombolysis|April 20, 2006
Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literatureA Girolami, F Tezza, M Scapin, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Effect of cellulose acetate 0.2 micron filter on platelet specific proteins plasma levelsF Stevanato, R Paolini, F Fabris, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1979
[Coagulation factors and blood platelets. (Presence and location of factor VIII and of fibrinogen in normal human platelets and in patients with coagulation disorders, using an immunofluorescence technic)]F Fabris, C Betterle, A Casonato, et al.
Acta Haematologica|January 1, 1987
The significance of thrombocytosis in old ageM L Randi, A Casonato, F Fabris, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1980
Normal platelet adhesiveness and aggregation in congenital PTA or Hageman factor deficiencyA Girolami, A Casonato, M Randi, et al.
Thrombosis Research|August 8, 2015
Severe, recessive type 1 is a discrete form of von Willebrand disease: the lesson learned from the c.1534-3C>A von Willebrand factor mutationA Casonato, M G Cattini, G Barbon, et al.
Thrombosis and Haemostasis|October 18, 1993
Platelet aggregation induced by plasma from type IIB von Willebrand's disease patients is associated with an increase in cytosolic Ca2+ concentrationM A Francesconi, R Deana, A Girolami, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 30, 2009
Uneventful coronary artery bypass surgery without prophylactic replacement therapy in a patient with a novel heterozygous FVII gene deletionL Gallinaro, A Casonato, F Vianello, et al.
Minerva Medica|May 26, 1980
[Juvenile rheumatoid arthritis appearing after hepatitis. Causal or casual relationship]G Amadori, A Milano, F Adami, et al.
Thrombosis and Haemostasis|July 10, 1998
On the release of von Willebrand factor from endothelial cells after venous occlusionA Casonato, E Pontara, A Bertomoro, et al.
Journal of Thrombosis and Thrombolysis|April 20, 2006
Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literatureA Girolami, F Tezza, M Scapin, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Effect of cellulose acetate 0.2 micron filter on platelet specific proteins plasma levelsF Stevanato, R Paolini, F Fabris, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1979
[Coagulation factors and blood platelets. (Presence and location of factor VIII and of fibrinogen in normal human platelets and in patients with coagulation disorders, using an immunofluorescence technic)]F Fabris, C Betterle, A Casonato, et al.
Acta Haematologica|January 1, 1987
The significance of thrombocytosis in old ageM L Randi, A Casonato, F Fabris, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1980
Normal platelet adhesiveness and aggregation in congenital PTA or Hageman factor deficiencyA Girolami, A Casonato, M Randi, et al.
Thrombosis Research|August 8, 2015
Severe, recessive type 1 is a discrete form of von Willebrand disease: the lesson learned from the c.1534-3C>A von Willebrand factor mutationA Casonato, M G Cattini, G Barbon, et al.
Thrombosis and Haemostasis|October 18, 1993
Platelet aggregation induced by plasma from type IIB von Willebrand's disease patients is associated with an increase in cytosolic Ca2+ concentrationM A Francesconi, R Deana, A Girolami, et al.
Pageof 12