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Publicaciones - CARDIOLOGIA CLINICA Y EXPERIMENTAL

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Arroyo-Úcar E, Moreno R, García E, Teles R, Rumoroso JR, Carvalho HC, Goicolea FJ, Moreu J, Mauri J, Sabaté M, Mainar V, Patricio L, Valdés M, Fernández-Vázquez F, Sánchez-Recalde A, Galeote G, Jimenez-Valero S, Almeida M, López de Sa E, Calvo L, Plaza I, Lopez-Sendón JL, Martín JL; CIBELES investigators.. Drug-eluting stent thrombosis in the treatment of chronic total coronary occlusions: incidence, presentation and related factors. Data from the CIBELES trial. Rev Port Cardiol. 2015 Mar;34(3):193-9. doi: 10.1016/j.repc.2014.08.026. PubMed PMID: 25686520.
AÑO: 2015; IF: 0.873
Hernández-Romero D, Jover E, Martínez CM, Andreu-Cayuelas JM, Orenes-Piñero E, Romero-Aniorte AI, Casas T, Cánovas S, Montero-Argudo JA, Valdés M, de la Morena G, Marín F. TWEAK and NT-proBNP levels predict exercise capacity in hypertrophic cardiomyopathy. Eur J Clin Invest. 2015 Feb;45(2):179-86. doi: 10.1111/eci.12394. PubMed PMID: 25524713.
AÑO: 2015; IF: 2.687
Cohen-Solal A, Laribi S, Ishihara S, Vergaro G, Baudet M, Logeart D, Mebazaa A, Gayat E, Vodovar N, Pascual-Figal DA, Seronde MF. Prognostic markers of acute decompensated heart failure: the emerging roles of cardiac biomarkers and prognostic scores. Arch Cardiovasc Dis. 2015 Jan;108(1):64-74. doi: 10.1016/j.acvd.2014.10.002. Review. PubMed PMID: 25534886.
AÑO: 2015; IF: 2.271
SEC Working Group for the ESC 2014 Guidelines on the Diagnosis and Management of Acute Pulmonary Embolism.; Expert Reviewers for the ESC 2014 Guidelines on the Diagnosis and Management of Acute Pulmonary Embolism.; SEC Clinical Practice Guidelines Committee.. Comments on the 2014 ESC Guidelines on the diagnosis and management of acute pulmonary embolism. Rev Esp Cardiol (Engl Ed). 2015 Jan;68(1):10-6. doi: 10.1016/j.rec.2014.11.003. PubMed PMID: 25553936.
AÑO: 2015; IF: 4.596
Muñoz-Esparza C, García-Molina E, Salar-Alcaraz M, Peñafiel-Verdú P, Sánchez-Muñoz JJ, Martínez Sánchez J, Cabañas-Perianes V, Valdés Chávarri M, García Alberola A, Gimeno-Blanes JR. Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. Rev Esp Cardiol (Engl Ed). 2015 Oct;68(10):861-8. doi: 10.1016/j.rec.2014.10.022. PubMed PMID: 25819988.
AÑO: 2015; IF: 4.596
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