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G Castaman

Showing results (161-170 of 198) with videos related to

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British Journal of Haematology|June 1, 1993
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocketG Marchetti, P Patracchini, D Gemmati, et al.
Journal of Thrombosis and Haemostasis : JTH|October 16, 2010
Laboratory diagnosis of von Willebrand disease: results from a prospective and blind study in 32 laboratories worldwide using lyophilized plasmasC A Lee, A Hubbard, C A Sabin, et al.
Journal of Thrombosis and Haemostasis : JTH|February 5, 2015
No evidence for a direct effect of von Willebrand factor's ABH blood group antigens on von Willebrand factor clearanceD J Groeneveld, T van Bekkum, K L Cheung, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 13, 2016
Low bleeding rates with increase or maintenance of physical activity in patients treated with recombinant factor VIII Fc fusion protein (rFVIIIFc) in the A-LONG and Kids A-LONG StudiesD V Quon, R Klamroth, R Kulkarni, et al.
Thrombosis Research|December 13, 2006
Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiencyG Castaman, E Biguzzi, C Razzari, et al.
Thrombosis and Haemostasis|June 1, 1994
Thrombosis during pregnancy and surgery in patients with congenital deficiency of antithrombin III, protein C, protein SV De Stefano, G Leone, S Mastrangelo, et al.
Thrombosis and Haemostasis|September 1, 1994
Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein SV De Stefano, G Leone, S Mastrangelo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.
Thrombosis and Haemostasis|February 3, 1992
Markers of procoagulant imbalance in patients with inherited thrombophilic syndromesP M Mannucci, A Tripodi, B Bottasso, et al.
Journal of Thrombosis and Haemostasis : JTH|June 22, 2011
Deep intronic variations may cause mild hemophilia AG Castaman, S H Giacomelli, M E Mancuso, et al.
Pageof 20

Showing results (161-170 of 198) with videos related to

Sort By:
Pageof 20
British Journal of Haematology|June 1, 1993
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocketG Marchetti, P Patracchini, D Gemmati, et al.
Journal of Thrombosis and Haemostasis : JTH|October 16, 2010
Laboratory diagnosis of von Willebrand disease: results from a prospective and blind study in 32 laboratories worldwide using lyophilized plasmasC A Lee, A Hubbard, C A Sabin, et al.
Journal of Thrombosis and Haemostasis : JTH|February 5, 2015
No evidence for a direct effect of von Willebrand factor's ABH blood group antigens on von Willebrand factor clearanceD J Groeneveld, T van Bekkum, K L Cheung, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 13, 2016
Low bleeding rates with increase or maintenance of physical activity in patients treated with recombinant factor VIII Fc fusion protein (rFVIIIFc) in the A-LONG and Kids A-LONG StudiesD V Quon, R Klamroth, R Kulkarni, et al.
Thrombosis Research|December 13, 2006
Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiencyG Castaman, E Biguzzi, C Razzari, et al.
Thrombosis and Haemostasis|June 1, 1994
Thrombosis during pregnancy and surgery in patients with congenital deficiency of antithrombin III, protein C, protein SV De Stefano, G Leone, S Mastrangelo, et al.
Thrombosis and Haemostasis|September 1, 1994
Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein SV De Stefano, G Leone, S Mastrangelo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.
Thrombosis and Haemostasis|February 3, 1992
Markers of procoagulant imbalance in patients with inherited thrombophilic syndromesP M Mannucci, A Tripodi, B Bottasso, et al.
Journal of Thrombosis and Haemostasis : JTH|June 22, 2011
Deep intronic variations may cause mild hemophilia AG Castaman, S H Giacomelli, M E Mancuso, et al.
Pageof 20