Publicaciones en colaboración con investigadores/as de University of Nottingham (4)

2024

  1. Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches

    Journal of Extracellular Vesicles, Vol. 13, Núm. 2

2021

  1. Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys Variant

    Clinical Reviews in Allergy and Immunology, Vol. 60, Núm. 3, pp. 357-368

2020

  1. Factor XII in PMM2-CDG patients: Role of N-glycosylation in the secretion and function of the first element of the contact pathway

    Orphanet Journal of Rare Diseases, Vol. 15, Núm. 1

  2. The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant

    Frontiers in Genetics, Vol. 11