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Thrombosis and Haemostasis|January 26, 2012
Effects of oral anticoagulant therapy and haplotype 1 of the endothelial protein C receptor gene on activated protein C levelsPilar Medina, Elena Bonet, Silvia Navarro, et al.
Haematologica|April 12, 2008
Haplotypes of the EPCR gene, prothrombin levels, and the risk of venous thrombosis in carriers of the prothrombin G20210A mutationSilvia Navarro, Pilar Medina, Yolanda Mira, et al.
Journal of Thrombosis and Thrombolysis|February 16, 2020
Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical managementAndrés Moret, Ángel Zúñiga, Javier Marco Ayala, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|April 13, 2025
Predicting Thrombophilia in Preeclampsia: Is Universal Testing Necessary?Ana Belén Gálvez, Pedro Chorão, Ernesto M Talegón, et al.
International Journal of Molecular Sciences|August 13, 2020
Increase of Neutrophil Activation Markers in Venous Thrombosis-Contribution of Circulating Activated Protein CLaura Martos, Julia Oto, Álvaro Fernández-Pardo, et al.
Thrombosis and Haemostasis|April 30, 2004
Contribution of polymorphisms in the endothelial protein C receptor gene to soluble endothelial protein C receptor and circulating activated protein C levels, and thrombotic riskPilar Medina, Silvia Navarro, Amparo Estellés, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 23, 2013
Association of the thrombomodulin gene c.1418C>T polymorphism with thrombomodulin levels and with venous thrombosis riskSilvia Navarro, Pilar Medina, Elena Bonet, et al.
Thrombosis and Haemostasis|June 30, 2019
Identification of 58 Mutations (26 Novel) in 94 of 109 Symptomatic Spanish Probands with Protein C DeficiencyLaura Martos, Álvaro Fernández-Pardo, María F López-Fernández, et al.
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