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Muñoz-Esparza C, Zorio E, Domingo Valero D, Peñafiel-Verdú P, Sánchez-Muñoz JJ, García-Molina E, Sabater M, Navarro M, San-Román I, Pérez I, Santos JJ, Cabañas-Perianes V, Valdés M, Pascual D, García-Alberola A, Gimeno Blanes JR. Value of the "Standing Test" in the Diagnosis and Evaluation of Beta-blocker Therapy Response in Long QT Syndrome. Rev Esp Cardiol (Engl Ed). 2017 Nov;70(11):907-914. doi: 10.1016/j.rec.2017.01.006. Epub 2017 Feb 21. English, Spanish. PubMed PMID: 28233664.
AÑO: 2017; IF: 5.166
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28233664
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López-Cuenca D, Muñoz-Esparza C, Navarro Peñalver M, García Alberola A, Gimeno Blanes JR. Hypertrophic or hypertensive cardiomyopathy? Int J Cardiol. 2016 Jan 15;203:891-2. doi: 10.1016/j.ijcard.2015.11.071. Epub 2015 Nov 10. PubMed PMID: 26609686.
AÑO: 2016; IF: 6.189
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San Román I, Navarro M, Martínez F, Albert L, Polo L, Guardiola J, García-Molina E, Muñoz-Esparza C, López-Ayala JM, Sabater-Molina M, Gimeno JR. Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1. Clin Genet. 2016 Aug;90(2):171-6. doi: 10.1111/cge.12760. Epub 2016 Mar 23. PubMed PMID: 26857240.
AÑO: 2016; IF: 3.326
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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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González-Cánovas C, Muñoz-Esparza C, Oliva MJ, González-Carrillo J, López-Cuenca Á, Saura D, García-Navarro M, Espinosa MD, Caro C, Caballero L, Valdés M, de la Morena G. Severe aortic valve stenosis with low-gradient and preserved ejection fraction: a misclassification issue? Rev Esp Cardiol (Engl Ed). 2013 Apr;66(4):255-60. doi: 10.1016/j.rec.2012.08.010. PubMed PMID: 24775614.
AÑO: 2013
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