Publicacións nas que colabora con Esther Lourés Fraga (3)

2014

  1. A novel mutation in adamts13 of a child with upshaw-schulman syndrome

    Thrombosis and Haemostasis

  2. Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): A short review

    Thrombosis Research, Vol. 134, Núm. 6, pp. 1171-1175

2009

  1. Autosomal dominant C1149R von Willebrand disease: Phenotypic findings and their implications

    Haematologica, Vol. 94, Núm. 5, pp. 679-686