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G Castaman

Showing results (171-180 of 198) with videos related to

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Thrombosis and Haemostasis|January 1, 1996
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasmaB Lunghi, L Iacoviello, D Gemmati, et al.
Thrombosis and Haemostasis|February 11, 2000
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 familiesR Schneppenheim, A B Federici, U Budde, et al.
Blood|March 15, 1996
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemiaI Dianzani, E Garelli, C Dompè, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 5, 2011
Central nervous system bleeding in patients with rare bleeding disordersS M Siboni, E Zanon, G Sottilotta, et al.
Journal of Thrombosis and Haemostasis : JTH|October 27, 2018
Phase 3 study of recombinant von Willebrand factor in patients with severe von Willebrand disease who are undergoing elective surgeryF Peyvandi, A Mamaev, J-D Wang, et al.
Journal of Thrombosis and Haemostasis : JTH|June 14, 2018
An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF studyA Szederjesi, L Baronciani, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|May 25, 2010
von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levelsN Hickson, D Hampshire, P Winship, et al.
Thrombosis Research|January 15, 1992
In vivo experiments indicate that relatively high platelet deposition in von Willebrand's disease 'Vicenza' is caused by normal platelet-VWF levels rather than by high VWF-multimers in plasmaP A d'Alessio, G Castaman, F Rodeghiero, et al.
Thrombosis and Haemostasis|October 22, 1990
Platelet adhesion to collagen in subtypes of type I von Willebrand's disease is dependent on platelet von Willebrand factorP d'Alessio, J J Zwaginga, H C de Boer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia AM Franchini, D Girelli, O Olivieri, et al.
Pageof 20

Showing results (171-180 of 198) with videos related to

Sort By:
Pageof 20
Thrombosis and Haemostasis|January 1, 1996
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasmaB Lunghi, L Iacoviello, D Gemmati, et al.
Thrombosis and Haemostasis|February 11, 2000
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 familiesR Schneppenheim, A B Federici, U Budde, et al.
Blood|March 15, 1996
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemiaI Dianzani, E Garelli, C Dompè, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 5, 2011
Central nervous system bleeding in patients with rare bleeding disordersS M Siboni, E Zanon, G Sottilotta, et al.
Journal of Thrombosis and Haemostasis : JTH|October 27, 2018
Phase 3 study of recombinant von Willebrand factor in patients with severe von Willebrand disease who are undergoing elective surgeryF Peyvandi, A Mamaev, J-D Wang, et al.
Journal of Thrombosis and Haemostasis : JTH|June 14, 2018
An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF studyA Szederjesi, L Baronciani, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|May 25, 2010
von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levelsN Hickson, D Hampshire, P Winship, et al.
Thrombosis Research|January 15, 1992
In vivo experiments indicate that relatively high platelet deposition in von Willebrand's disease 'Vicenza' is caused by normal platelet-VWF levels rather than by high VWF-multimers in plasmaP A d'Alessio, G Castaman, F Rodeghiero, et al.
Thrombosis and Haemostasis|October 22, 1990
Platelet adhesion to collagen in subtypes of type I von Willebrand's disease is dependent on platelet von Willebrand factorP d'Alessio, J J Zwaginga, H C de Boer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Tyr2105Cys mutation in exon 22 of FVIII gene is a risk factor for the development of inhibitors in patients with mild/moderate haemophilia AM Franchini, D Girelli, O Olivieri, et al.
Pageof 20