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J A Aznar

Showing results (11-20 of 111) with videos related to

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Sangre|January 1, 1972
[Statistical comparison between prothrombin time, Owren's thrombotest and cephalin time during the surveillance of anticoagulant therapy]J Aznar, A Fernández Pavón, J A Aznar
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 24, 1999
Postoperative use of rFVIIa by continuous infusion in a haemophilic boyJ I Lorenzo, J M Montoro, J A Aznar
Sangre|January 1, 1982
[Standardization of the technic for the dosage of F. VIII: C (in a single step). Multicenter study of its reproducibility with participation of 23 Spanish hospitals. Phase II]J A Aznar, F Ortega, S de la Torre
Sangre|January 1, 1983
[Importance of corticoids in inhibitor suppression in hemophilia A, in addition to continuing treatment with factor VIII concentrate]J A Aznar, J I Jorquera, M L Marty
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.
Vision Research|April 20, 2013
Two stages of programming eye gaze shifts in 3-D spaceL Pérez Zapata, J A Aznar-Casanova, H Supèr
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Orthoses in haemophiliaF Querol, J A Aznar, S Haya, et al.
The Medical Journal of Australia|March 30, 1974
Letter: Thrombolytic therapy of the anuric stage of disseminated intravascular coagulationJ A Aznar, J Aznar, F Carbonell, et al.
British Journal of Haematology|May 31, 2001
Incidence of factor VIII inhibitors in severe haemophilia: the importance of patient ageJ I Lorenzo, A López, C Altisent, 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.
Pageof 12

Showing results (11-20 of 111) with videos related to

Sort By:
Pageof 12
Sangre|January 1, 1972
[Statistical comparison between prothrombin time, Owren's thrombotest and cephalin time during the surveillance of anticoagulant therapy]J Aznar, A Fernández Pavón, J A Aznar
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 24, 1999
Postoperative use of rFVIIa by continuous infusion in a haemophilic boyJ I Lorenzo, J M Montoro, J A Aznar
Sangre|January 1, 1982
[Standardization of the technic for the dosage of F. VIII: C (in a single step). Multicenter study of its reproducibility with participation of 23 Spanish hospitals. Phase II]J A Aznar, F Ortega, S de la Torre
Sangre|January 1, 1983
[Importance of corticoids in inhibitor suppression in hemophilia A, in addition to continuing treatment with factor VIII concentrate]J A Aznar, J I Jorquera, M L Marty
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.
Vision Research|April 20, 2013
Two stages of programming eye gaze shifts in 3-D spaceL Pérez Zapata, J A Aznar-Casanova, H Supèr
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Orthoses in haemophiliaF Querol, J A Aznar, S Haya, et al.
The Medical Journal of Australia|March 30, 1974
Letter: Thrombolytic therapy of the anuric stage of disseminated intravascular coagulationJ A Aznar, J Aznar, F Carbonell, et al.
British Journal of Haematology|May 31, 2001
Incidence of factor VIII inhibitors in severe haemophilia: the importance of patient ageJ I Lorenzo, A López, C Altisent, 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.
Pageof 12