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S Haya

Showing results (11-20 of 23) with videos related to

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British Journal of Haematology|December 21, 2000
Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor geneP Casaña, F Martínez, S Haya, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Zero incidence of inhibitor development in previously treated haemophilia A, HIV-negative patients upon exposure to a plasma-derived high-purity and double viral inactivated factor VIII concentrateJ A Aznar, J I Lorenzo, R Molina, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 31, 2008
Inhibitors in haemophilia A: current management and open issuesS Haya, A Moret, A R Cid, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 3, 2001
A comparison of FVII:C and FVIIa assays for the monitoring of recombinant factor VIIa treatmentA R Cid, J I Lorenzo, S Haya, et al.
Revista Clinica Espanola|June 1, 1996
[Effect of factor VIII concentrates of very high purity on CD4+ cell count in hemophiliacs infected with HIV]R Molina Alejandro, J I Lorenzo Herrero, S Haya Guaita, et al.
Sangre|October 1, 1996
[Seroprevalence of hepatitis A in hemophiliacs]R Molina, J I Lorenzo, M D Gómez, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
European study on orthopaedic status of haemophilia patients with inhibitorsM Morfini, S Haya, G Tagariello, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 11, 2008
One-stage and chromogenic FVIII:C assay discrepancy in mild haemophilia A and the relationship with the mutation and bleeding phenotypeA R Cid, M Calabuig, V Cortina, et al.
Journal of Thrombosis and Thrombolysis|July 4, 2019
Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiencyA Moret, Ángel Zúñiga, M Ibáñez, et al.
Sangre|February 1, 1993
[3 families with a congenital factor X deficiency, one of them with an associated factor XII deficiency]M Pérez Sánchez, J López, J L López, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
British Journal of Haematology|December 21, 2000
Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor geneP Casaña, F Martínez, S Haya, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Zero incidence of inhibitor development in previously treated haemophilia A, HIV-negative patients upon exposure to a plasma-derived high-purity and double viral inactivated factor VIII concentrateJ A Aznar, J I Lorenzo, R Molina, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 31, 2008
Inhibitors in haemophilia A: current management and open issuesS Haya, A Moret, A R Cid, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 3, 2001
A comparison of FVII:C and FVIIa assays for the monitoring of recombinant factor VIIa treatmentA R Cid, J I Lorenzo, S Haya, et al.
Revista Clinica Espanola|June 1, 1996
[Effect of factor VIII concentrates of very high purity on CD4+ cell count in hemophiliacs infected with HIV]R Molina Alejandro, J I Lorenzo Herrero, S Haya Guaita, et al.
Sangre|October 1, 1996
[Seroprevalence of hepatitis A in hemophiliacs]R Molina, J I Lorenzo, M D Gómez, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
European study on orthopaedic status of haemophilia patients with inhibitorsM Morfini, S Haya, G Tagariello, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 11, 2008
One-stage and chromogenic FVIII:C assay discrepancy in mild haemophilia A and the relationship with the mutation and bleeding phenotypeA R Cid, M Calabuig, V Cortina, et al.
Journal of Thrombosis and Thrombolysis|July 4, 2019
Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiencyA Moret, Ángel Zúñiga, M Ibáñez, et al.
Sangre|February 1, 1993
[3 families with a congenital factor X deficiency, one of them with an associated factor XII deficiency]M Pérez Sánchez, J López, J L López, et al.
Pageof 3