Publications in collaboration with researchers from Hospital Sierrallana (2)

2006

  1. Mutation study of spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of endoglin and ALK1

    Human Mutation, Vol. 27, Núm. 3

2004

  1. Mutation analysis in Spanish patients with hereditary hemorrhagic telangiectasia: Deficient endoglin up-regulation in activated monocytes

    Clinical Chemistry, Vol. 50, Núm. 11, pp. 2003-2011