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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 gene
P 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 concentrate
J 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 issues
S 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 treatment
A 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 inhibitors
M 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 phenotype
A 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 deficiency
A 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.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
British Journal of Haematology
|
December 21, 2000
Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene
P 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 concentrate
J 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 issues
S 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 treatment
A 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 inhibitors
M 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 phenotype
A 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 deficiency
A 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.
Page
of 3