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G Castaman

Showing results (61-70 of 198) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|March 8, 2005
A novel fibrinogen gamma chain mutation (gamma 239 Gln-->His) is the cause of dysfibrinogenemia VicenzaG Castaman, R Ghiotto, S Duga, et al.
Journal of Thrombosis and Haemostasis : JTH|January 27, 2005
Bbeta 14 Arg --> Cys variant dysfibrinogen and its association with thrombosisG Castaman, R Ghiotto, A Tosetto, et al.
British Journal of Haematology|May 1, 1996
High-dose dexamethasone in adult refractory idiopathic thrombocytopenic purpuraC Schiavotto, M Ruggeri, G Castaman, et al.
British Journal of Haematology|August 12, 1999
Pseudohomozygosity for activated protein C resistance is a risk factor for venous thrombosisG Castaman, A Tosetto, M Ruggeri, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1985
[Therapy with high-dose intravenous gamma globulin in the newborn infant with thrombocytopenia from passive immunization]G F Ronconi, G Castaman, E Fantuz, et al.
Thrombosis and Haemostasis|November 1, 2000
Grossly abnormal proteolysis of von Willebrand factor (VWF) in a patient heterozygous for a gene deletion and mutation in the dimerization area of VWFG Castaman, J C Eikenboom, A Lattuada, et al.
American Journal of Hematology|May 1, 1993
Desmopressin-induced thrombocytopenia in type I platelet discordant von Willebrand diseaseG Castaman, F Rodeghiero, A Lattuada, et al.
British Journal of Haematology|January 1, 1995
Factor VIII:C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand diseaseG Castaman, A Lattuada, P M Mannucci, et al.
Thrombosis and Haemostasis|January 23, 1992
Subunit composition of plasma von Willebrand factor (vWF) in two uremic patients with acquired vWF abnormalitiesG Castaman, F Rodeghiero, A Lattuada, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 9, 2008
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutationsG Castaman, S H Giacomelli, S Duga, et al.
Pageof 20

Showing results (61-70 of 198) with videos related to

Sort By:
Pageof 20
Journal of Thrombosis and Haemostasis : JTH|March 8, 2005
A novel fibrinogen gamma chain mutation (gamma 239 Gln-->His) is the cause of dysfibrinogenemia VicenzaG Castaman, R Ghiotto, S Duga, et al.
Journal of Thrombosis and Haemostasis : JTH|January 27, 2005
Bbeta 14 Arg --> Cys variant dysfibrinogen and its association with thrombosisG Castaman, R Ghiotto, A Tosetto, et al.
British Journal of Haematology|May 1, 1996
High-dose dexamethasone in adult refractory idiopathic thrombocytopenic purpuraC Schiavotto, M Ruggeri, G Castaman, et al.
British Journal of Haematology|August 12, 1999
Pseudohomozygosity for activated protein C resistance is a risk factor for venous thrombosisG Castaman, A Tosetto, M Ruggeri, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1985
[Therapy with high-dose intravenous gamma globulin in the newborn infant with thrombocytopenia from passive immunization]G F Ronconi, G Castaman, E Fantuz, et al.
Thrombosis and Haemostasis|November 1, 2000
Grossly abnormal proteolysis of von Willebrand factor (VWF) in a patient heterozygous for a gene deletion and mutation in the dimerization area of VWFG Castaman, J C Eikenboom, A Lattuada, et al.
American Journal of Hematology|May 1, 1993
Desmopressin-induced thrombocytopenia in type I platelet discordant von Willebrand diseaseG Castaman, F Rodeghiero, A Lattuada, et al.
British Journal of Haematology|January 1, 1995
Factor VIII:C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand diseaseG Castaman, A Lattuada, P M Mannucci, et al.
Thrombosis and Haemostasis|January 23, 1992
Subunit composition of plasma von Willebrand factor (vWF) in two uremic patients with acquired vWF abnormalitiesG Castaman, F Rodeghiero, A Lattuada, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 9, 2008
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutationsG Castaman, S H Giacomelli, S Duga, et al.
Pageof 20