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Bauduer F, de la Morena-Barrio ME, Salloum-Asfar S, de la Morena-Barrio B, Padilla J, Minano A, Vicente V, Carbonell P, Corral J, Esteban J. When genetic and surname analyses meet historical sources: The C56R mutation associated with factor XI deficiency as a marker of human migration during the Spanish Reconquista. Med Hypotheses. 2020 Aug;141:109709. doi: 10.1016/j.mehy.2020.109709. Epub 2020 Apr 6. PubMed PMID: 32278893.
AÑO: 2020; IF: 1.538
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32278893
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de la Morena-Barrio ME. Commentary on Acquired Factor XI Deficiency during SARS-CoV-2 Infection: Not Only Thrombosis. TH Open. 2020 Sep 13;4(3):e231-e232. doi: 10.1055/s-0040-1716839. eCollection 2020 Jul. No abstract available. PubMed PMID: 32939440; PubMed Central PMCID: PMC7487213.
AÑO: 2020
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Lopez-Galvez R, de la Morena-Barrio ME, Lopez-Lera A, Pathak M, Minano A, Serrano M, Borgel D, Roldan V, Vicente V, Emsley J, Corral J. Factor XII in PMM2-CDG patients: role of N-glycosylation in the secretion and function of the first element of the contact pathway. Orphanet J Rare Dis. 2020 Oct 9;15(1):280. doi: 10.1186/s13023-020-01564-9. PubMed PMID: 33036649; PubMed Central PMCID: PMC7547467.
AÑO: 2020; IF: 4.123
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Corvillo F, de la Morena-Barrio ME, Marcos-Bravo C, Lopez-Trascasa M, Vicente V, Emsley J, Caballero T, Corral J, Lopez-Lera A. The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant. Front Genet. 2020 Sep 10;11:1033. doi: 10.3389/fgene.2020.01033. eCollection 2020. PubMed PMID: 33133137; PubMed Central PMCID: PMC7549737.
AÑO: 2020; IF: 4.599
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Bravo-Perez C, de la Morena-Barrio ME, Vicente V, Corral J. Antithrombin deficiency as a still underdiagnosed thrombophilia: a primer for internists. Pol Arch Intern Med. 2020 Oct 29;130(10):868-877. doi: 10.20452/pamw.15371. Epub 2020 May 19. PubMed PMID: 32426958.
AÑO: 2020; IF: 3.277
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