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G Castaman

Showing results (81-90 of 198) with videos related to

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Thrombosis Research|February 1, 1992
A new variant of von Willebrand disease (type II I) with a normal degree of proteolytic cleavage of von Willebrand factorG Castaman, F Rodeghiero, A Lattuada, et al.
Thrombosis and Haemostasis|August 26, 2000
Pregnancy in women with type 1 von Willebrand disease caused by heterozygosity for von Willebrand factor mutation C1130FG Castaman, J C Eikenboom, A Contri, et al.
American Journal of Hematology|May 1, 1995
Characterization of two cases of acquired transitory von Willebrand syndrome with ciprofloxacin: evidence for heightened proteolysis of von Willebrand factorG Castaman, A Lattuada, P M Mannucci, et al.
Blood|November 1, 1989
Consistency of responses to repeated DDAVP infusions in patients with von Willebrand's disease and hemophilia AF Rodeghiero, G Castaman, E Di Bona, et al.
Blut|April 1, 1989
Clinical effectiveness of desmopressin in a case of acquired von Willebrand's syndrome associated with benign monoclonal gammopathyG Castaman, F Rodeghiero, E Di Bona, et al.
Blood|June 15, 1992
Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: a cross-over randomized trialP M Mannucci, P M Tenconi, G Castaman, et al.
Blut|March 1, 1988
Erythema multiforme after intravenous immunoglobulinF Rodeghiero, G Castaman, M Vespignani, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 10, 2000
The A20210 allele in the prothrombin gene enhances the risk of venous thrombosis in carriers of inherited protein S deficiencyG Castaman, A Tosetto, A Cappellari, et al.
Thrombosis and Haemostasis|September 24, 1999
Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigationG Castaman, J C Eikenboom, R M Bertina, et al.
Blood|November 1, 1996
The Ser460Pro substitution of the protein S (PS) gene in rare in Italian patients with type IIa PS deficiencyG Castaman, M Ruggeri, A Tosetto, et al.
Pageof 20

Showing results (81-90 of 198) with videos related to

Sort By:
Pageof 20
Thrombosis Research|February 1, 1992
A new variant of von Willebrand disease (type II I) with a normal degree of proteolytic cleavage of von Willebrand factorG Castaman, F Rodeghiero, A Lattuada, et al.
Thrombosis and Haemostasis|August 26, 2000
Pregnancy in women with type 1 von Willebrand disease caused by heterozygosity for von Willebrand factor mutation C1130FG Castaman, J C Eikenboom, A Contri, et al.
American Journal of Hematology|May 1, 1995
Characterization of two cases of acquired transitory von Willebrand syndrome with ciprofloxacin: evidence for heightened proteolysis of von Willebrand factorG Castaman, A Lattuada, P M Mannucci, et al.
Blood|November 1, 1989
Consistency of responses to repeated DDAVP infusions in patients with von Willebrand's disease and hemophilia AF Rodeghiero, G Castaman, E Di Bona, et al.
Blut|April 1, 1989
Clinical effectiveness of desmopressin in a case of acquired von Willebrand's syndrome associated with benign monoclonal gammopathyG Castaman, F Rodeghiero, E Di Bona, et al.
Blood|June 15, 1992
Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: a cross-over randomized trialP M Mannucci, P M Tenconi, G Castaman, et al.
Blut|March 1, 1988
Erythema multiforme after intravenous immunoglobulinF Rodeghiero, G Castaman, M Vespignani, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 10, 2000
The A20210 allele in the prothrombin gene enhances the risk of venous thrombosis in carriers of inherited protein S deficiencyG Castaman, A Tosetto, A Cappellari, et al.
Thrombosis and Haemostasis|September 24, 1999
Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigationG Castaman, J C Eikenboom, R M Bertina, et al.
Blood|November 1, 1996
The Ser460Pro substitution of the protein S (PS) gene in rare in Italian patients with type IIa PS deficiencyG Castaman, M Ruggeri, A Tosetto, et al.
Pageof 20