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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 haemophiliac
S 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 gene
P 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 disease
P 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 history
J 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 method
J 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 patients
P Casaña, F Martínez, N Cabrera, et al.
Haematologica
|
October 12, 2000
Haemophilia B in a female caused by skewed inactivation of the normal X-chromosome
C Espinós, J I Lorenzo, P Casaña, et al.
Page
of 12
Search research articles
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Showing results (31-40 of 111) with videos related to
Sort By:
Page
of 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 haemophiliac
S 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 gene
P 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 disease
P 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 history
J 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 method
J 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 patients
P Casaña, F Martínez, N Cabrera, et al.
Haematologica
|
October 12, 2000
Haemophilia B in a female caused by skewed inactivation of the normal X-chromosome
C Espinós, J I Lorenzo, P Casaña, et al.
Page
of 12