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G Castaman

Showing results (151-160 of 198) with videos related to

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British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
Thrombosis Research|February 15, 1993
Supranormal antithrombin III levels induced by concentrate administration are ineffective in quenching thrombin generation in acute promyelocytic leukemiaF Rodeghiero, G Castaman, L Gugliotta, et al.
Blood|November 11, 1999
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)E M Faioni, F Franchi, P Bucciarelli, et al.
British Journal of Haematology|February 1, 1994
The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand diseaseE Fressinaud, A B Federici, G Castaman, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2012
Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formationG Castaman, S H Giacomelli, P M Jacobi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 12, 2013
The spectrum of factor XI deficiency in ItalyG Castaman, S H Giacomelli, S Caccia, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 5, 2011
Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiencyG Castaman, S H Giacomelli, V Schroeder, et al.
Leukemia|March 1, 1993
Alpha (p55) and beta (p75) chains of the interleukin-2 receptor are expressed by AML blastsG Pizzolo, A Rigo, R Zanotti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 6, 2007
F8 gene mutation profile and ITT response in a cohort of Italian haemophilia A patients with inhibitorsR Salviato, D Belvini, P Radossi, et al.
Journal of Thrombosis and Haemostasis : JTH|October 7, 2009
Pharmacokinetics and safety of fibrinogen concentrateM J Manco-Johnson, D Dimichele, G Castaman, et al.
Pageof 20

Showing results (151-160 of 198) with videos related to

Sort By:
Pageof 20
British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
Thrombosis Research|February 15, 1993
Supranormal antithrombin III levels induced by concentrate administration are ineffective in quenching thrombin generation in acute promyelocytic leukemiaF Rodeghiero, G Castaman, L Gugliotta, et al.
Blood|November 11, 1999
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)E M Faioni, F Franchi, P Bucciarelli, et al.
British Journal of Haematology|February 1, 1994
The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand diseaseE Fressinaud, A B Federici, G Castaman, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2012
Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formationG Castaman, S H Giacomelli, P M Jacobi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 12, 2013
The spectrum of factor XI deficiency in ItalyG Castaman, S H Giacomelli, S Caccia, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 5, 2011
Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiencyG Castaman, S H Giacomelli, V Schroeder, et al.
Leukemia|March 1, 1993
Alpha (p55) and beta (p75) chains of the interleukin-2 receptor are expressed by AML blastsG Pizzolo, A Rigo, R Zanotti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 6, 2007
F8 gene mutation profile and ITT response in a cohort of Italian haemophilia A patients with inhibitorsR Salviato, D Belvini, P Radossi, et al.
Journal of Thrombosis and Haemostasis : JTH|October 7, 2009
Pharmacokinetics and safety of fibrinogen concentrateM J Manco-Johnson, D Dimichele, G Castaman, et al.
Pageof 20