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G Castaman

Showing results (101-110 of 198) with videos related to

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Haematologica|November 1, 1993
Adult patients with the nephrotic syndrome: really at high risk for deep venous thromboembolism? Report of a series and review of the literatureM Ruggeri, M Milan, G La Greca, et al.
Thrombosis and Haemostasis|August 26, 2000
An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutationG Castaman, E Missiaglia, A B Federici, et al.
Haematologica|November 1, 1991
Long-lasting remission after high-dose intravenous immunoglobulins in a case of relapsing thrombotic thrombocytopenic purpuraG Castaman, F Rodeghiero, M Ruggeri, et al.
Thrombosis and Haemostasis|October 5, 2001
Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosisG Castaman, A Tosetto, M Simioni, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 2, 2009
Severe spontaneous arterial thrombotic manifestations in patients with inherited hypo- and afibrinogenemiaG Castaman, M Lunardi, L Rigo, et al.
Haematologica|January 1, 1991
Fibrinolytic studies in 13 unrelated families with factor XII deficiencyF Rodeghiero, G Castaman, M Ruggeri, et al.
Haematologica|May 1, 1992
A follow-up study of 49 adult patients with idiopathic thrombocytopenic purpura treated with high-dose immunoglobulins and anti-D immunoglobulinsF Rodeghiero, C Schiavotto, G Castaman, et al.
British Journal of Haematology|March 1, 1995
A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopeniaG Castaman, J C Eikenboom, F Rodeghiero, et al.
Journal of Thrombosis and Haemostasis : JTH|March 5, 2008
Prevalence of type 2b 'Malmö/New York' von Willebrand disease in Italy: the role of von Willebrand factor gene conversionL Baronciani, A B Federici, G Castaman, et al.
Journal of Thrombosis and Haemostasis : JTH|April 19, 2007
von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: a prospective multicenter trial in elective surgeryS Lethagen, P A Kyrle, G Castaman, et al.
Pageof 20

Showing results (101-110 of 198) with videos related to

Sort By:
Pageof 20
Haematologica|November 1, 1993
Adult patients with the nephrotic syndrome: really at high risk for deep venous thromboembolism? Report of a series and review of the literatureM Ruggeri, M Milan, G La Greca, et al.
Thrombosis and Haemostasis|August 26, 2000
An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutationG Castaman, E Missiaglia, A B Federici, et al.
Haematologica|November 1, 1991
Long-lasting remission after high-dose intravenous immunoglobulins in a case of relapsing thrombotic thrombocytopenic purpuraG Castaman, F Rodeghiero, M Ruggeri, et al.
Thrombosis and Haemostasis|October 5, 2001
Phenotypic APC resistance in carriers of the A20210 prothrombin mutation is associated with an increased risk of venous thrombosisG Castaman, A Tosetto, M Simioni, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 2, 2009
Severe spontaneous arterial thrombotic manifestations in patients with inherited hypo- and afibrinogenemiaG Castaman, M Lunardi, L Rigo, et al.
Haematologica|January 1, 1991
Fibrinolytic studies in 13 unrelated families with factor XII deficiencyF Rodeghiero, G Castaman, M Ruggeri, et al.
Haematologica|May 1, 1992
A follow-up study of 49 adult patients with idiopathic thrombocytopenic purpura treated with high-dose immunoglobulins and anti-D immunoglobulinsF Rodeghiero, C Schiavotto, G Castaman, et al.
British Journal of Haematology|March 1, 1995
A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopeniaG Castaman, J C Eikenboom, F Rodeghiero, et al.
Journal of Thrombosis and Haemostasis : JTH|March 5, 2008
Prevalence of type 2b 'Malmö/New York' von Willebrand disease in Italy: the role of von Willebrand factor gene conversionL Baronciani, A B Federici, G Castaman, et al.
Journal of Thrombosis and Haemostasis : JTH|April 19, 2007
von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: a prospective multicenter trial in elective surgeryS Lethagen, P A Kyrle, G Castaman, et al.
Pageof 20