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G Castaman

Showing results (41-50 of 198) with videos related to

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Thrombosis and Haemostasis|November 1, 1996
Prospective multicenter study on subcutaneous concentrated desmopressin for home treatment of patients with von Willebrand disease and mild or moderate hemophilia AF Rodeghiero, G Castaman, P M Mannucci
Thrombosis and Haemostasis|April 1, 1994
Angiodysplasia and von Willebrand's diseaseG Castaman, E Di Bona, F Rodeghiero
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 10, 1997
Inherited abnormalities of blood coagulation in juvenile stroke. A case-control studyA Tosetto, M Ruggeri, G Castaman, et al.
Thrombosis and Haemostasis|May 4, 1992
Thrombosis in subjects with homozygous and heterozygous factor XII deficiencyF Rodeghiero, G Castaman, M Ruggeri, et al.
Haematologica|July 1, 1989
Juvenile essential thrombocythemia: really a benign disease?G Castaman, F Rodeghiero, A D'Emilio, et al.
Thrombosis and Haemostasis|August 26, 2000
Heterogeneity of activated protein C resistance phenotype in subjects with compound heterozygosity for HR2 haplotype and FV Leiden mutation (R506Q) in factor V geneG Castaman, M Ruggeri, A Tosetto, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 30, 2002
Guidelines for the diagnosis and management of von Willebrand disease in ItalyA B Federici, G Castaman, P M Mannucci, et al.
Thrombosis and Haemostasis|December 29, 2000
The VITA Project: heritability of resistance to activated protein C. Vincenza Thrombophilia and ArteriosclerosisA Tosetto, G Castaman, A Cappellari, et al.
Thrombosis Research|February 1, 1993
High levels of histidine-rich glycoprotein and thrombotic diathesis. Report of two unrelated familiesG Castaman, M Ruggeri, F Burei, et al.
Lancet (London, England)|March 29, 2001
Congenital absence of the inferior vena cava: a rare risk factor for idiopathic deep-vein thrombosisM Ruggeri, A Tosetto, G Castaman, et al.
Pageof 20

Showing results (41-50 of 198) with videos related to

Sort By:
Pageof 20
Thrombosis and Haemostasis|November 1, 1996
Prospective multicenter study on subcutaneous concentrated desmopressin for home treatment of patients with von Willebrand disease and mild or moderate hemophilia AF Rodeghiero, G Castaman, P M Mannucci
Thrombosis and Haemostasis|April 1, 1994
Angiodysplasia and von Willebrand's diseaseG Castaman, E Di Bona, F Rodeghiero
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 10, 1997
Inherited abnormalities of blood coagulation in juvenile stroke. A case-control studyA Tosetto, M Ruggeri, G Castaman, et al.
Thrombosis and Haemostasis|May 4, 1992
Thrombosis in subjects with homozygous and heterozygous factor XII deficiencyF Rodeghiero, G Castaman, M Ruggeri, et al.
Haematologica|July 1, 1989
Juvenile essential thrombocythemia: really a benign disease?G Castaman, F Rodeghiero, A D'Emilio, et al.
Thrombosis and Haemostasis|August 26, 2000
Heterogeneity of activated protein C resistance phenotype in subjects with compound heterozygosity for HR2 haplotype and FV Leiden mutation (R506Q) in factor V geneG Castaman, M Ruggeri, A Tosetto, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 30, 2002
Guidelines for the diagnosis and management of von Willebrand disease in ItalyA B Federici, G Castaman, P M Mannucci, et al.
Thrombosis and Haemostasis|December 29, 2000
The VITA Project: heritability of resistance to activated protein C. Vincenza Thrombophilia and ArteriosclerosisA Tosetto, G Castaman, A Cappellari, et al.
Thrombosis Research|February 1, 1993
High levels of histidine-rich glycoprotein and thrombotic diathesis. Report of two unrelated familiesG Castaman, M Ruggeri, F Burei, et al.
Lancet (London, England)|March 29, 2001
Congenital absence of the inferior vena cava: a rare risk factor for idiopathic deep-vein thrombosisM Ruggeri, A Tosetto, G Castaman, et al.
Pageof 20