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J A Aznar

Showing results (31-40 of 111) with videos related to

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Revista Clinica Espanola|August 31, 1973
[Contributions to the biological diagnosis of disseminated intravascular coagulation (apropos of a case of DIC in an acute promyelocytic leukemia)]J A Aznar, J Mayans, J Aznar, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Development of a factor VIII inhibitor in a newborn haemophiliacS Haya, J I Lorenzo, M A Dasí, et al.
British Journal of Haematology|December 12, 2001
Significant linkage and non-linkage of type 1 von Willebrand disease to the von Willebrand factor geneP Casaña, F Martínez, S Haya, et al.
Annals of Hematology|September 1, 2001
Association of the 3467C>T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's diseaseP Casaña, F Martínez, S Haya, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 3, 2000
Diagnosis of two related carriers of severe haemophilia B with no family historyJ I Lorenzo, P Casaña, C Espinós, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 13, 2009
Clinical and echographical control protocol of haemarthrosis in haemophilia patients with inhibitors: evaluation of the efficacy of recombinant factor VIIa in the evolution process (EFFISEVEN protocol)F Querol, V Cortina, A R Cid, et al.
Thrombosis Research|March 15, 1990
Immunological characterization of factor VIII inhibitors by a sensitive micro-ELISA methodJ M Sánchez-Cuenca, E Carmona, M J Villanueva, et al.
Sangre|January 1, 1973
[Hageman factor deficiency. Apropos of a case]J Aznar, J Mayans, J A Aznar, et al.
Journal of Thrombosis and Haemostasis : JTH|April 19, 2008
Founder haplotype associated with the factor VIII Asp1241Glu polymorphism in a cohort of mild hemophilia A patientsP Casaña, F Martínez, N Cabrera, et al.
Haematologica|October 12, 2000
Haemophilia B in a female caused by skewed inactivation of the normal X-chromosomeC Espinós, J I Lorenzo, P Casaña, et al.
Pageof 12

Showing results (31-40 of 111) with videos related to

Sort By:
Pageof 12
Revista Clinica Espanola|August 31, 1973
[Contributions to the biological diagnosis of disseminated intravascular coagulation (apropos of a case of DIC in an acute promyelocytic leukemia)]J A Aznar, J Mayans, J Aznar, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Development of a factor VIII inhibitor in a newborn haemophiliacS Haya, J I Lorenzo, M A Dasí, et al.
British Journal of Haematology|December 12, 2001
Significant linkage and non-linkage of type 1 von Willebrand disease to the von Willebrand factor geneP Casaña, F Martínez, S Haya, et al.
Annals of Hematology|September 1, 2001
Association of the 3467C>T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's diseaseP Casaña, F Martínez, S Haya, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 3, 2000
Diagnosis of two related carriers of severe haemophilia B with no family historyJ I Lorenzo, P Casaña, C Espinós, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 13, 2009
Clinical and echographical control protocol of haemarthrosis in haemophilia patients with inhibitors: evaluation of the efficacy of recombinant factor VIIa in the evolution process (EFFISEVEN protocol)F Querol, V Cortina, A R Cid, et al.
Thrombosis Research|March 15, 1990
Immunological characterization of factor VIII inhibitors by a sensitive micro-ELISA methodJ M Sánchez-Cuenca, E Carmona, M J Villanueva, et al.
Sangre|January 1, 1973
[Hageman factor deficiency. Apropos of a case]J Aznar, J Mayans, J A Aznar, et al.
Journal of Thrombosis and Haemostasis : JTH|April 19, 2008
Founder haplotype associated with the factor VIII Asp1241Glu polymorphism in a cohort of mild hemophilia A patientsP Casaña, F Martínez, N Cabrera, et al.
Haematologica|October 12, 2000
Haemophilia B in a female caused by skewed inactivation of the normal X-chromosomeC Espinós, J I Lorenzo, P Casaña, et al.
Pageof 12