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G Castaman

Showing results (121-130 of 198) with videos related to

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Blut|August 1, 1989
Clinical significance of fibrinopeptide A in acute lymphocytic and non-lymphocytic leukaemiaF Rodeghiero, G Castaman, G Soffiati, et al.
Human Molecular Genetics|July 1, 1994
Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-->Val) and X (334Ser-->Pro)F Bernardi, G Castaman, R Redaelli, et al.
British Journal of Haematology|April 29, 2006
Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand diseaseP Tjernberg, G Castaman, H L Vos, et al.
European Journal of Haematology|February 1, 1988
Hyper-responsiveness to DDAVP for patients with type I von Willebrand's disease and normal intra-platelet von Willebrand factorF Rodeghiero, G Castaman, E Di Bona, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2004
Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residuesP Tjernberg, H L Vos, G Castaman, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 20, 2010
F8 mRNA studies in haemophilia A patients with different splice site mutationsG Castaman, S H Giacomelli, M E Mancuso, et al.
American Journal of Hematology|November 17, 2006
Autosomal recessive von Willebrand disease associated with compound heterozygosity for a novel nonsense mutation (2908 del C) and the missense mutation C2362F: definite evidence for the non-penetrance of the C2362F mutationG Castaman, K Bertoncello, M Bernardi, et al.
Minerva Stomatologica|March 7, 1998
[Prevention of hemorrhage and dental treatment of patients with congenital or acquired coagulopathies]R Vangelisti, O Pagnacco, G Ristagno, et al.
British Journal of Haematology|February 13, 2001
The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or bothI Martinelli, P Bucciarelli, M Margaglione, et al.
Journal of Thrombosis and Haemostasis : JTH|December 15, 2010
Effect of the VWF promoter (GT)n repeat and single-nucleotide polymorphism c.-2527G>A on circulating von Willebrand factor levels under normal conditionsN Hickson, D Hampshire, G Castaman, et al.
Pageof 20

Showing results (121-130 of 198) with videos related to

Sort By:
Pageof 20
Blut|August 1, 1989
Clinical significance of fibrinopeptide A in acute lymphocytic and non-lymphocytic leukaemiaF Rodeghiero, G Castaman, G Soffiati, et al.
Human Molecular Genetics|July 1, 1994
Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-->Val) and X (334Ser-->Pro)F Bernardi, G Castaman, R Redaelli, et al.
British Journal of Haematology|April 29, 2006
Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand diseaseP Tjernberg, G Castaman, H L Vos, et al.
European Journal of Haematology|February 1, 1988
Hyper-responsiveness to DDAVP for patients with type I von Willebrand's disease and normal intra-platelet von Willebrand factorF Rodeghiero, G Castaman, E Di Bona, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2004
Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residuesP Tjernberg, H L Vos, G Castaman, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 20, 2010
F8 mRNA studies in haemophilia A patients with different splice site mutationsG Castaman, S H Giacomelli, M E Mancuso, et al.
American Journal of Hematology|November 17, 2006
Autosomal recessive von Willebrand disease associated with compound heterozygosity for a novel nonsense mutation (2908 del C) and the missense mutation C2362F: definite evidence for the non-penetrance of the C2362F mutationG Castaman, K Bertoncello, M Bernardi, et al.
Minerva Stomatologica|March 7, 1998
[Prevention of hemorrhage and dental treatment of patients with congenital or acquired coagulopathies]R Vangelisti, O Pagnacco, G Ristagno, et al.
British Journal of Haematology|February 13, 2001
The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or bothI Martinelli, P Bucciarelli, M Margaglione, et al.
Journal of Thrombosis and Haemostasis : JTH|December 15, 2010
Effect of the VWF promoter (GT)n repeat and single-nucleotide polymorphism c.-2527G>A on circulating von Willebrand factor levels under normal conditionsN Hickson, D Hampshire, G Castaman, et al.
Pageof 20