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S Haya

Showing results (1-10 of 23) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Orthoses in haemophiliaF Querol, J A Aznar, S Haya, et al.
American Journal of Hematology|April 15, 1999
Identification of a new candidate mutation, G1629R, in a family with type 2A von Willebrand diseaseP Casaña, F Martínez, S Haya, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 22, 2001
Immune tolerance treatment in haemophilia patients with inhibitors: the Spanish RegistryS Haya, M F López, J A Aznar, et al.
Haematologica|April 28, 2001
New mutations in exon 28 of the von Willebrand factor gene detected in patients with different types of von Willebrand's diseaseP Casaña, F Martínez, S Haya, 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|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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 9, 2007
Inhibitor development in one patient and laboratory discrepancies in several families with both mild haemophilia and Arg531Cys mutationA R Cid, P Casaña, N Cabrera, et al.
American Journal of Hematology|September 2, 1998
Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: new mutations, R1315C and R1341W, associated with type 2M and 2B variantsP Casaña, F Martínez, C Espinós, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Orthoses in haemophiliaF Querol, J A Aznar, S Haya, et al.
American Journal of Hematology|April 15, 1999
Identification of a new candidate mutation, G1629R, in a family with type 2A von Willebrand diseaseP Casaña, F Martínez, S Haya, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 22, 2001
Immune tolerance treatment in haemophilia patients with inhibitors: the Spanish RegistryS Haya, M F López, J A Aznar, et al.
Haematologica|April 28, 2001
New mutations in exon 28 of the von Willebrand factor gene detected in patients with different types of von Willebrand's diseaseP Casaña, F Martínez, S Haya, 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|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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 9, 2007
Inhibitor development in one patient and laboratory discrepancies in several families with both mild haemophilia and Arg531Cys mutationA R Cid, P Casaña, N Cabrera, et al.
American Journal of Hematology|September 2, 1998
Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: new mutations, R1315C and R1341W, associated with type 2M and 2B variantsP Casaña, F Martínez, C Espinós, et al.
Pageof 3