Maria Eugenia De La Morena Barrio-rekin lankidetzan egindako argitalpenak (8)

2023

  1. Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases

    International Journal of Molecular Sciences, Vol. 24, Núm. 22

2021

  1. Anticoagulant therapy in patients with congenital FXI deficiency

    Blood Advances, Vol. 5, Núm. 20, pp. 4083-4086

2020

  1. ALG12-CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant

    Molecular Genetics and Genomic Medicine, Vol. 8, Núm. 8

  2. 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. Assessment of two contact activation reagents for the diagnosis of congenital factor XI deficiency

    Thrombosis Research, Vol. 163, pp. 64-70

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. Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect

    Journal of Thrombosis and Haemostasis, Vol. 14, Núm. 8, pp. 1549-1560

2015

  1. A new method to quantify β-antithrombin glycoform in plasma reveals increased levels during the acute stroke event

    Thrombosis Research, Vol. 136, Núm. 3, pp. 634-641