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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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26857240
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Jiménez-Jáimez J, Peinado R, Grima EZ, Segura F, Moriña P, Sánchez Muñoz JJ, Mazuelos F, Cózar R, Gimeno JR, Heras RP, Monserrat L, Domingo D, Ortiz-Genga M, Fernández Pastor J, Álvarez M, Tercedor L. Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study). Am J Cardiol. 2015 Sep 15;116(6):894-9. doi: 10.1016/j.amjcard.2015.06.030. PubMed PMID: 26189708.
AÑO: 2015; IF: 3.154
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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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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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Pastor Quirante FA, Pastor-Pérez FJ, Manzano-Fernández S, Rivas NL, Pérez PP, Hernández JP, Gimeno-Blanes JR. Unexpected autopsy findings after sudden cardiac death: cardiovascular myxoedema and endocardial fibroelastosis. Int J Cardiol. 2015 Mar 1;182:281-3. doi: 10.1016/j.ijcard.2014.12.156. PubMed PMID: 25585372.
AÑO: 2015; IF: 4.638
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