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García-Botella A, Asenjo S, De la Morena-Barrio ME, Corral J, Bolaños E, Carlin PS, López ES, García AJ. First case with antithrombin deficiency, mesenteric vein thrombosis and pregnancy: Multidisciplinary diagnosis and successful management. Thromb Res. 2016 Aug;144:72-5. doi: 10.1016/j.thromres.2016.05.011. Epub 2016 Jun 3. PubMed PMID: 27304580.
AÑO: 2016; IF: 2.65
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27304580
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Dasi MA, Gonzalez-Conejero R, Izquierdo S, Padilla J, Garcia JL, Garcia-Barberá N, Argilés B, de la Morena-Barrio ME, Hernández-Sánchez JM, Hernández-Rivas JM, Vicente V, Corral J. Uniparental disomy causes deficiencies of vitamin K-dependent proteins. J Thromb Haemost. 2016 Dec;14(12):2410-2418. doi: 10.1111/jth.13517. Epub 2016 Nov 19. PubMed PMID: 27681307.
AÑO: 2016; IF: 5.287
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Vossen CY, van Hylckama Vlieg A, Teruel-Montoya R, Salloum-Asfar S, de Haan H, Corral J, Reitsma P, Koeleman BPC, Martínez C. Identification of coagulation gene 3'UTR variants that are potentially regulated by microRNAs. Br J Haematol. 2017 Jun;177(5):782-790. doi: 10.1111/bjh.14629. Epub 2017 Apr 26. PubMed PMID: 28444748.
AÑO: 2017; IF: 5.128
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Zeng W, Hu B, Tang L, You YY, Toderici M, de la Morena-Barrio ME, Corral J, Hu Y. Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency. Oncotarget. 2017 Sep 28;8(48):84417-84425. doi: 10.18632/oncotarget.21365. eCollection 2017 Oct 13. Erratum in: Oncotarget. 2018 Feb 16;9(13):11428. PubMed PMID: 29137435; PubMed Central PMCID: PMC5663607.
AÑO: 2017; IF: 5.168
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Esteban J, de la Morena-Barrio ME, Salloum-Asfar S, Padilla J, Miñano A, Roldán V, Soria JM, Vidal F, Corral J, Vicente V. 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. 2017 Nov;23(6):e488-e496. doi: 10.1111/hae.13356. Epub 2017 Sep 27. PubMed PMID: 28960694.
AÑO: 2017; IF: 2.768
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