Raquel López Gálvez-rekin lankidetzan egindako argitalpenak (6)

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

2018

  1. Genetic predisposition to fetal alcohol syndrome: Association with congenital disorders of N-glycosylation

    Pediatric Research, Vol. 83, Núm. 1, pp. 119-127

2017

  1. Defects of splicing in antithrombin deficiency

    Research and Practice in Thrombosis and Haemostasis, Vol. 1, Núm. 2, pp. 216-222

  2. High levels of latent antithrombin in plasma from patients with antithrombin deficiency

    Thrombosis and Haemostasis, Vol. 117, Núm. 5, pp. 880-888

  3. Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy

    Scientific Reports, Vol. 7