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Rivera-Caravaca JM, Marin F, Vilchez JA, Galvez J, Esteve-Pastor MA, Vicente V, Lip GYH, Roldan V. Refining Stroke and Bleeding Prediction in Atrial Fibrillation by Adding Consecutive Biomarkers to Clinical Risk Scores. Stroke. 2019 Jun;50(6):1372-1379. doi: 10.1161/STROKEAHA.118.024305. Epub 2019 May 14. PubMed PMID: 31084333.
AÑO: 2019; IF: 10.17
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31084333
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de la Morena-Barrio ME, Salloum-Asfar S, Esteban J, de la Morena-Barrio B, Altisent C, Martin-Fernandez L, Gueguen P, Padilla J, Minano A, Parra R, Vicente V, Vidal F, Bauduer F, Carbonell P, Corral J. Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries. Blood. 2019 Jun 13;133(24):2618-2622. doi: 10.1182/blood.2019000055. Epub 2019 May 1. No abstract available. PubMed PMID: 31043424.
AÑO: 2019; IF: 25.476
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Bastida JM, Morais S, Palma-Barqueros V, Benito R, Bermejo N, Karkucak M, Trapero-Marugan M, Bohdan N, Pereira M, Marin-Quilez A, Oliveira J, Yucel Y, Santos R, Padilla J, Janusz K, Lau C, Martin-Izquierdo M, Couto E, Francisco Ruiz-Pividal J, Vicente V, Hernandez-Rivas JM, Gonzalez-Porras JR, Luisa Lozano M, Lima M, Rivera J. Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing. Ann Med. 2019 Mar;51(2):141-148. doi: 10.1080/07853890.2019.1587498. Epub 2019 Apr 16. PubMed PMID: 30990103; PubMed Central PMCID: PMC7857454.
AÑO: 2019; IF: 3.243
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de la Morena-Barrio B, Orlando C, de la Morena-Barrio ME, Vicente V, Jochmans K, Corral J. Incidence and features of thrombosis in children with inherited antithrombin deficiency. Haematologica. 2019 Dec;104(12):2512-2518. doi: 10.3324/haematol.2018.210666. Epub 2019 Apr 11. PubMed PMID: 30975910; PubMed Central PMCID: PMC6959168.
AÑO: 2019; IF: 7.116
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De la Morena-Barrio B, Borras N, Rodriguez-Alen A, de la Morena-Barrio ME, Garcia-Hernandez JL, Padilla J, Bravo-Perez C, Minano A, Rollon N, Corral J, Vidal F, Vicente V. Identification of the first large intronic deletion responsible of type I antithrombin deficiency not detected by routine molecular diagnostic methods. Br J Haematol. 2019 Aug;186(4):e82-e86. doi: 10.1111/bjh.15913. Epub 2019 Apr 2. No abstract available. PubMed PMID: 30941754.
AÑO: 2019; IF: 5.518
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