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A Casonato

Showing results (11-20 of 115) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|November 9, 2017
Type 2N von Willebrand disease: Characterization and diagnostic difficultiesA Casonato, E Galletta, L Sarolo, et al.
Blut|May 1, 1987
Increased factor VIII/vWf levels in patients with reduced platelet numberA Casonato, F Fabris, M Boscaro, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 14, 2001
Early transfusion of factor VIII/von Willebrand factor concentrates seems to be effective in the treatment of gastrointestinal bleeding in patients with von Willebrand type III diseaseE Zanon, F Vianello, A Casonato, et al.
Computer Methods and Programs in Biomedicine|August 25, 2019
A framework for the optimal design of a minimum set of clinical trials to characterize von Willebrand diseaseB Taverna, A Casonato, F Bezzo, et al.
Acta Haematologica|January 1, 1986
Acquired type I von Willebrand's disease in a patient with essential thrombocytosisA Casonato, F Fabris, L Zancan, et al.
Acta Haematologica|January 1, 1988
Factor VIII/von Willebrand factor abnormalities during L-asparaginase treatment in patients with acute lymphoblastic leukemiaA Casonato, A R Lazzaro, A Rosolen, et al.
Acta Haematologica|January 1, 1980
Increased number of pseudodrumsticks in neutrophils and large platelets. A "new' congenital leukocyte and platelet morphological abnormalityA Girolami, F Fabris, A Casonato, et al.
Clinical and Laboratory Haematology|January 1, 1982
Potentiation of anticoagulant response to warfarin by sulphinpyrazone: a double-blind study in patients with prosthetic heart valvesA Girolami, F Fabris, A Casonato, et al.
Acta Haematologica|January 1, 1982
Thrombocytopenia secondary to oxprenolol, a beta-blocking agentG M Patrassi, A Casonato, F Fabris, et al.
Haemostasis|January 1, 1980
Plasma and platelet beta-thromboglobulin levels in patients with May-Hegglin anomalyF Fabris, A Casonato, M L Randi, et al.
Pageof 12

Showing results (11-20 of 115) with videos related to

Sort By:
Pageof 12
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 9, 2017
Type 2N von Willebrand disease: Characterization and diagnostic difficultiesA Casonato, E Galletta, L Sarolo, et al.
Blut|May 1, 1987
Increased factor VIII/vWf levels in patients with reduced platelet numberA Casonato, F Fabris, M Boscaro, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 14, 2001
Early transfusion of factor VIII/von Willebrand factor concentrates seems to be effective in the treatment of gastrointestinal bleeding in patients with von Willebrand type III diseaseE Zanon, F Vianello, A Casonato, et al.
Computer Methods and Programs in Biomedicine|August 25, 2019
A framework for the optimal design of a minimum set of clinical trials to characterize von Willebrand diseaseB Taverna, A Casonato, F Bezzo, et al.
Acta Haematologica|January 1, 1986
Acquired type I von Willebrand's disease in a patient with essential thrombocytosisA Casonato, F Fabris, L Zancan, et al.
Acta Haematologica|January 1, 1988
Factor VIII/von Willebrand factor abnormalities during L-asparaginase treatment in patients with acute lymphoblastic leukemiaA Casonato, A R Lazzaro, A Rosolen, et al.
Acta Haematologica|January 1, 1980
Increased number of pseudodrumsticks in neutrophils and large platelets. A "new' congenital leukocyte and platelet morphological abnormalityA Girolami, F Fabris, A Casonato, et al.
Clinical and Laboratory Haematology|January 1, 1982
Potentiation of anticoagulant response to warfarin by sulphinpyrazone: a double-blind study in patients with prosthetic heart valvesA Girolami, F Fabris, A Casonato, et al.
Acta Haematologica|January 1, 1982
Thrombocytopenia secondary to oxprenolol, a beta-blocking agentG M Patrassi, A Casonato, F Fabris, et al.
Haemostasis|January 1, 1980
Plasma and platelet beta-thromboglobulin levels in patients with May-Hegglin anomalyF Fabris, A Casonato, M L Randi, et al.
Pageof 12