Publicaciones en colaboración con investigadores/as de Hospital de la Santa Creu i Sant Pau (5)

2019

  1. Archeogenetics of F11 p.Cys38Arg: A 5400-year-old mutation identified in different southwestern European countries

    Blood

2017

  1. High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study

    Haemophilia, Vol. 23, Núm. 6, pp. e488-e496

2016

  1. Antithrombin Dublin (p.Val30Glu): A relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency

    Thrombosis and Haemostasis, Vol. 116, Núm. 1, pp. 146-154

2012

  1. Regulatory regions of SERPINC1 gene: Identification of the first mutation associated with antithrombin deficiency

    Thrombosis and Haemostasis, Vol. 107, Núm. 3, pp. 430-437

2011

  1. Soluble ST2 is a marker for acute cardiac allograft rejection

    Annals of Thoracic Surgery, Vol. 92, Núm. 6, pp. 2118-2124