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Haematologica
|
April 11, 2000
Platelet function during cardiopulmonary bypass not changed by two different doses of aprotinin
A Santamaría, J Mateo, E Muñíz-Díaz, et al.
Inorganic Chemistry
|
October 8, 2021
High-Temperature Synthesis and Dielectric Properties of LaTaON<sub>2</sub>
Augustin Castets, Ignasi Fina, Jhonatan R Guarín, et al.
Thrombosis and Haemostasis
|
March 8, 2003
Prothrombin G20210A mutation and oral contraceptive use increase upper-extremity deep vein thrombotic risk
Amparo Vayá, Yolanda Mira, Jose Mateo, et al.
Thrombosis and Haemostasis
|
October 6, 1998
The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population
J C Souto, I Coll, D Llobet, et al.
Plant Physiology
|
December 10, 2024
CAX-INTERACTING PROTEIN4 depletion causes early lethality and pre-mRNA missplicing in Arabidopsis
Uri Aceituno-Valenzuela, Sara Fontcuberta-Cervera, Rosa Micol-Ponce, et al.
Thrombosis and Haemostasis
|
October 31, 1988
Plasma and urinary heparin cofactor II levels in patients with nephrotic syndrome
E Grau, A Oliver, J Félez, et al.
Thrombosis and Haemostasis
|
November 5, 2005
Rapid identification of female haemophilia A carriers with deletions in the factor VIII gene by quantitative real-time PCR analysis
Eduardo F Tizzano, María J Barceló, Manel Baena, et al.
ACS Applied Materials & Interfaces
|
August 19, 2020
Plasma-Enhanced Atomic Layer Deposition of Nickel Nanotubes with Low Resistivity and Coherent Magnetization Dynamics for 3D Spintronics
M C Giordano, K Baumgaertl, S Escobar Steinvall, et al.
Medicina Clinica
|
November 30, 1996
[Isolated thrombocytopenia in pregnancy. Etiopathogenic study and therapeutic approach in 60 patients]
A Altès, E Muñiz-Díaz, N Pujol-Moix, et al.
Thrombosis and Haemostasis
|
June 1, 1996
Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC gene
J M Soria, L P Berg, J Fontcuberta, et al.
Page
of 45
Search research articles
Search
Showing results (201-210 of 449) with videos related to
Sort By:
Page
of 45
Haematologica
|
April 11, 2000
Platelet function during cardiopulmonary bypass not changed by two different doses of aprotinin
A Santamaría, J Mateo, E Muñíz-Díaz, et al.
Inorganic Chemistry
|
October 8, 2021
High-Temperature Synthesis and Dielectric Properties of LaTaON<sub>2</sub>
Augustin Castets, Ignasi Fina, Jhonatan R Guarín, et al.
Thrombosis and Haemostasis
|
March 8, 2003
Prothrombin G20210A mutation and oral contraceptive use increase upper-extremity deep vein thrombotic risk
Amparo Vayá, Yolanda Mira, Jose Mateo, et al.
Thrombosis and Haemostasis
|
October 6, 1998
The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population
J C Souto, I Coll, D Llobet, et al.
Plant Physiology
|
December 10, 2024
CAX-INTERACTING PROTEIN4 depletion causes early lethality and pre-mRNA missplicing in Arabidopsis
Uri Aceituno-Valenzuela, Sara Fontcuberta-Cervera, Rosa Micol-Ponce, et al.
Thrombosis and Haemostasis
|
October 31, 1988
Plasma and urinary heparin cofactor II levels in patients with nephrotic syndrome
E Grau, A Oliver, J Félez, et al.
Thrombosis and Haemostasis
|
November 5, 2005
Rapid identification of female haemophilia A carriers with deletions in the factor VIII gene by quantitative real-time PCR analysis
Eduardo F Tizzano, María J Barceló, Manel Baena, et al.
ACS Applied Materials & Interfaces
|
August 19, 2020
Plasma-Enhanced Atomic Layer Deposition of Nickel Nanotubes with Low Resistivity and Coherent Magnetization Dynamics for 3D Spintronics
M C Giordano, K Baumgaertl, S Escobar Steinvall, et al.
Medicina Clinica
|
November 30, 1996
[Isolated thrombocytopenia in pregnancy. Etiopathogenic study and therapeutic approach in 60 patients]
A Altès, E Muñiz-Díaz, N Pujol-Moix, et al.
Thrombosis and Haemostasis
|
June 1, 1996
Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC gene
J M Soria, L P Berg, J Fontcuberta, et al.
Page
of 45