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Medicina Clinica
|
April 18, 1987
[Congenital protein C deficiency in patients with thromboembolic disease. Study of 4 Spanish families]
N Sala, E Muñiz, M Borrell, et al.
Annals of Hematology
|
July 1, 1997
Late hemorrhagic disease of the newborn as a cause of intracerebral bleeding
P Solves, A Altés, G Ginovart, et al.
Physical Review Letters
|
January 17, 2012
Chiral domains in cycloidal multiferroic thin films: switching and memory effects
I Fina, L Fàbrega, X Martí, et al.
Thrombosis and Haemostasis
|
March 1, 1997
Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism--results of the Spanish Multicentric Study on Thrombophilia (EMET-Study)
J Mateo, A Oliver, M Borrell, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
June 11, 1998
Tissue factor pathway inhibitor and anti-FXa kinetic profiles of a new low-molecular-mass heparin, Bemiparin, at therapeutic subcutaneous doses
L Falkon, M Garí, M Barbanoj, et al.
Haemostasis
|
January 1, 1990
Fibrinogen Barcelona II: a new case of A alpha 16 Arg----His substitution
M Borrell, L Vila, J Solá, et al.
Scientific Reports
|
October 24, 2012
High mobility conduction at (110) and (111) LaAlO3/SrTiO3 interfaces
G Herranz, F Sánchez, N Dix, et al.
Thrombosis Research
|
May 1, 1992
Familial elevation of plasma histidine-rich glycoprotein. A case associated with recurrent venous thrombosis and high PAI-1 levels
L Falkon, M Gari, I Montserrat, et al.
European Journal of Respiratory Diseases
|
August 1, 1986
Diffuse pulmonary hemorrhage associated with anticoagulant therapy
M Santalo, P Domingo, J Fontcuberta, et al.
Thrombosis and Haemostasis
|
July 15, 2000
Massive skin necrosis associated to the prothrombin gene G20210A mutation
V García-Patos, J C Souto, A Castells, et al.
Page
of 18
Search research articles
Search
Showing results (31-40 of 172) with videos related to
Sort By:
Page
of 18
Medicina Clinica
|
April 18, 1987
[Congenital protein C deficiency in patients with thromboembolic disease. Study of 4 Spanish families]
N Sala, E Muñiz, M Borrell, et al.
Annals of Hematology
|
July 1, 1997
Late hemorrhagic disease of the newborn as a cause of intracerebral bleeding
P Solves, A Altés, G Ginovart, et al.
Physical Review Letters
|
January 17, 2012
Chiral domains in cycloidal multiferroic thin films: switching and memory effects
I Fina, L Fàbrega, X Martí, et al.
Thrombosis and Haemostasis
|
March 1, 1997
Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism--results of the Spanish Multicentric Study on Thrombophilia (EMET-Study)
J Mateo, A Oliver, M Borrell, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
June 11, 1998
Tissue factor pathway inhibitor and anti-FXa kinetic profiles of a new low-molecular-mass heparin, Bemiparin, at therapeutic subcutaneous doses
L Falkon, M Garí, M Barbanoj, et al.
Haemostasis
|
January 1, 1990
Fibrinogen Barcelona II: a new case of A alpha 16 Arg----His substitution
M Borrell, L Vila, J Solá, et al.
Scientific Reports
|
October 24, 2012
High mobility conduction at (110) and (111) LaAlO3/SrTiO3 interfaces
G Herranz, F Sánchez, N Dix, et al.
Thrombosis Research
|
May 1, 1992
Familial elevation of plasma histidine-rich glycoprotein. A case associated with recurrent venous thrombosis and high PAI-1 levels
L Falkon, M Gari, I Montserrat, et al.
European Journal of Respiratory Diseases
|
August 1, 1986
Diffuse pulmonary hemorrhage associated with anticoagulant therapy
M Santalo, P Domingo, J Fontcuberta, et al.
Thrombosis and Haemostasis
|
July 15, 2000
Massive skin necrosis associated to the prothrombin gene G20210A mutation
V García-Patos, J C Souto, A Castells, et al.
Page
of 18