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Identification of 58 Mutations (26 Novel) in 94 of 109 Symptomatic Spanish Probands with Protein C Deficiency.
Martos L, Fernández-Pardo Á, López-Fernández MF, Ibáñez F, Herrero S, Tàssies D, González-Porras JR, Solmoirago MJ, Costa MJ, Reverter JC, Marco P, Roldán V, Lecumberri R, Velasco F, Oto J, Iruin G, Alonso MN, Vayá A, Bonanad S, Ferrando F, Martí E, Cid AR, Plana E, Oña F, Cuesta I, González-López TJ, España F, Medina P, Navarro S; Working Group of the Spanish Society of Thrombosis Haemostasis (SETH). Martos L, et al. Among authors: navarro s. Thromb Haemost. 2019 Sep;119(9):1409-1418. doi: 10.1055/s-0039-1692440. Epub 2019 Jun 29. Thromb Haemost. 2019. PMID: 31254973
Inherited abnormalities in the protein C activation pathway.
España F, Medina P, Navarro S, Estellés A, Aznar J. España F, et al. Among authors: navarro s. Pathophysiol Haemost Thromb. 2002 Sep-Dec;32(5-6):241-4. doi: 10.1159/000073573. Pathophysiol Haemost Thromb. 2002. PMID: 13679649 Review.
Contribution of polymorphisms in the endothelial protein C receptor gene to soluble endothelial protein C receptor and circulating activated protein C levels, and thrombotic risk.
Medina P, Navarro S, Estellés A, Vayá A, Woodhams B, Mira Y, Villa P, Migaud-Fressart M, Ferrando F, Aznar J, Bertina RM, España F. Medina P, et al. Among authors: navarro s. Thromb Haemost. 2004 May;91(5):905-11. doi: 10.1160/TH03-10-0657. Thromb Haemost. 2004. PMID: 15116250
1,161 results