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Items: 1 to 20 of 53

1.

Left ventricular myocardial dysfunction in arrhythmogenic cardiomyopathy with left ventricular involvement: A door to improving diagnosis.

Vives-Gilabert Y, Sanz-Sánchez J, Molina P, Cebrián A, Igual B, Calvillo-Batllés P, Domingo D, Millet J, Martínez-Dolz L, Castells F, Zorio E.

Int J Cardiol. 2018 Sep 10. pii: S0167-5273(18)33417-X. doi: 10.1016/j.ijcard.2018.09.024. [Epub ahead of print]

2.

Thickness and an Altered miRNA Expression in the Epicardial Adipose Tissue Is Associated With Coronary Heart Disease in Sudden Death Victims.

Marí-Alexandre J, Barceló-Molina M, Sanz-Sánchez J, Molina P, Sancho J, Abellán Y, Santaolaria-Ayora ML, Giner J, Martínez-Dolz L, Estelles A, Braza-Boïls A, Zorio E.

Rev Esp Cardiol (Engl Ed). 2018 Feb 10. pii: S1885-5857(17)30601-1. doi: 10.1016/j.rec.2017.12.007. [Epub ahead of print] English, Spanish.

PMID:
29439878
3.

Direct oral anticoagulants in patients with hypertrophic cardiomyopathy and atrial fibrillation.

Dominguez F, Climent V, Zorio E, Ripoll-Vera T, Salazar-Mendiguchía J, García-Pinilla JM, Urbano-Moral JA, Fernández-Fernández X, Lopez-Cuenca D, Ajo-Ferrer R, Sanz-Sanchez J, Gomez-Perez Y, López-Garrido MA, Barriales-Villa R, Gimeno JR, Garcia-Pavia P.

Int J Cardiol. 2017 Dec 1;248:232-238. doi: 10.1016/j.ijcard.2017.08.010. Epub 2017 Aug 7.

PMID:
28811092
4.

RyR2R420Q catecholaminergic polymorphic ventricular tachycardia mutation induces bradycardia by disturbing the coupled clock pacemaker mechanism.

Wang YY, Mesirca P, Marqués-Sulé E, Zahradnikova A Jr, Villejoubert O, D'Ocon P, Ruiz C, Domingo D, Zorio E, Mangoni ME, Benitah JP, Gómez AM.

JCI Insight. 2017 Apr 20;2(8). pii: 91872. doi: 10.1172/jci.insight.91872. [Epub ahead of print]

5.

Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection.

Gago-Díaz M, Ramos-Luis E, Zoppis S, Zorio E, Molina P, Braza-Boïls A, Giner J, Sobrino B, Amigo J, Blanco-Verea A, Carracedo Á, Brion M.

Int J Legal Med. 2017 Sep;131(5):1211-1219. doi: 10.1007/s00414-017-1583-9. Epub 2017 Apr 8.

PMID:
28391405
6.

Myocardial Extracellular Volume Is Not Associated With Malignant Ventricular Arrhythmias in High-risk Hypertrophic Cardiomyopathy.

Mirelis JG, Sánchez-González J, Zorio E, Ripoll-Vera T, Salguero-Bodes R, Filgueiras-Rama D, González-López E, Gallego-Delgado M, Fernández-Jiménez R, Soleto MJ, Núñez J, Pizarro G, Sanz J, Fuster V, García-Pavía P, Ibáñez B.

Rev Esp Cardiol (Engl Ed). 2017 Nov;70(11):933-940. doi: 10.1016/j.rec.2017.01.026. Epub 2017 Mar 22. English, Spanish.

PMID:
28341414
7.

Value of the "Standing Test" in the Diagnosis and Evaluation of Beta-blocker Therapy Response in Long QT Syndrome.

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.

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.

PMID:
28233664
8.

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.

Ortiz-Genga MF, Cuenca S, Dal Ferro M, Zorio E, Salgado-Aranda R, Climent V, Padrón-Barthe L, Duro-Aguado I, Jiménez-Jáimez J, Hidalgo-Olivares VM, García-Campo E, Lanzillo C, Suárez-Mier MP, Yonath H, Marcos-Alonso S, Ochoa JP, Santomé JL, García-Giustiniani D, Rodríguez-Garrido JL, Domínguez F, Merlo M, Palomino J, Peña ML, Trujillo JP, Martín-Vila A, Stolfo D, Molina P, Lara-Pezzi E, Calvo-Iglesias FE, Nof E, Calò L, Barriales-Villa R, Gimeno-Blanes JR, Arad M, García-Pavía P, Monserrat L.

J Am Coll Cardiol. 2016 Dec 6;68(22):2440-2451. doi: 10.1016/j.jacc.2016.09.927.

9.

Deregulated hepatic microRNAs underlie the association between non-alcoholic fatty liver disease and coronary artery disease.

Braza-Boïls A, Marí-Alexandre J, Molina P, Arnau MA, Barceló-Molina M, Domingo D, Girbes J, Giner J, Martínez-Dolz L, Zorio E.

Liver Int. 2016 Aug;36(8):1221-9. doi: 10.1111/liv.13097. Epub 2016 Mar 23.

PMID:
26901384
10.

Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.

Nunn LM, Lopes LR, Syrris P, Murphy C, Plagnol V, Firman E, Dalageorgou C, Zorio E, Domingo D, Murday V, Findlay I, Duncan A, Carr-White G, Robert L, Bueser T, Langman C, Fynn SP, Goddard M, White A, Bundgaard H, Ferrero-Miliani L, Wheeldon N, Suvarna SK, O'Beirne A, Lowe MD, McKenna WJ, Elliott PM, Lambiase PD.

Europace. 2016 Jun;18(6):888-96. doi: 10.1093/europace/euv285. Epub 2015 Oct 25.

11.

Phenotypic Patterns of Cardiomyopathy Caused by Mutations in the Desmin Gene. A Clinical and Genetic Study in Two Inherited Heart Disease Units.

Ripoll-Vera T, Zorio E, Gámez JM, Molina P, Govea N, Crémer D.

Rev Esp Cardiol (Engl Ed). 2015 Nov;68(11):1027-9. doi: 10.1016/j.rec.2015.07.007. Epub 2015 Oct 1. No abstract available.

PMID:
26431784
12.

Sensitivity and negative predictive value of treadmill exercise stress testing for the diagnosis of catecholaminergic polymorphic ventricular tachycardia. Response.

Domingo D, López-Vilella R, Arnau MÁ, Zorio E.

Rev Esp Cardiol (Engl Ed). 2015 Jun;68(6):546-7. doi: 10.1016/j.rec.2015.02.011. Epub 2015 May 1. No abstract available.

PMID:
25936659
13.

The genetic background of left ventricular hypertrabeculation/noncompaction remains vague. Response.

Rodríguez-Serrano M, Domingo D, Igual B, Zorio E.

Rev Esp Cardiol (Engl Ed). 2015 Feb;68(2):167-8. doi: 10.1016/j.rec.2014.10.001. Epub 2014 Dec 15. No abstract available.

PMID:
25522834
14.

Non-ventricular, Clinical, and Functional Features of the RyR2(R420Q) Mutation Causing Catecholaminergic Polymorphic Ventricular Tachycardia.

Domingo D, Neco P, Fernández-Pons E, Zissimopoulos S, Molina P, Olagüe J, Suárez-Mier MP, Lai FA, Gómez AM, Zorio E.

Rev Esp Cardiol (Engl Ed). 2015 May;68(5):398-407. doi: 10.1016/j.rec.2014.04.023. Epub 2014 Nov 29.

PMID:
25440180
15.

A new mutation in the ryanodine receptor 2 gene (RYR2 C2277R) as a cause catecholaminergic polymorphic ventricular tachycardia.

Domingo D, López-Vilella R, Arnau MÁ, Cano Ó, Fernández-Pons E, Zorio E.

Rev Esp Cardiol (Engl Ed). 2015 Jan;68(1):71-3. doi: 10.1016/j.rec.2014.07.022. Epub 2014 Nov 27. No abstract available.

PMID:
25435091
16.

Familial left ventricular noncompaction associated with a novel mutation in the alpha-cardiac actin gene.

Rodríguez-Serrano M, Domingo D, Igual B, Cano A, Medina P, Zorio E.

Rev Esp Cardiol (Engl Ed). 2014 Oct;67(10):857-9. doi: 10.1016/j.rec.2014.05.015. Epub 2014 Sep 5. No abstract available.

PMID:
25201647
17.

Role of novel DSP_p.Q986X genetic variation in arrhythmogenic right ventricular cardiomyopathy.

Campuzano O, Alcalde M, Berne P, Zorio E, Iglesias A, Navarro-Manchón J, Brugada J, Brugada R.

Eur J Med Genet. 2013 Oct;56(10):541-5. doi: 10.1016/j.ejmg.2013.08.001. Epub 2013 Aug 14.

PMID:
23954618
18.

Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy.

Núñez L, Gimeno-Blanes JR, Rodríguez-García MI, Monserrat L, Zorio E, Coats C, McGregor CG, Hernandez del Rincón JP, Castro-Beiras A, Hermida-Prieto M.

Circ J. 2013;77(9):2358-65. Epub 2013 Jun 19.

19.

Flecainide, a therapeutic option in a patient with long QT syndrome type 3 caused by the heterozygous V411M mutation in the SCN5A gene.

Carrasco JI, Izquierdo I, Medina P, Arnau MÁ, Salvador A, Zorio E.

Rev Esp Cardiol (Engl Ed). 2012 Nov;65(11):1058-9. doi: 10.1016/j.recesp.2012.03.014. Epub 2012 Jun 19. English, Spanish. No abstract available.

PMID:
22721569
20.

Paradoxical effect of increased diastolic Ca(2+) release and decreased sinoatrial node activity in a mouse model of catecholaminergic polymorphic ventricular tachycardia.

Neco P, Torrente AG, Mesirca P, Zorio E, Liu N, Priori SG, Napolitano C, Richard S, Benitah JP, Mangoni ME, Gómez AM.

Circulation. 2012 Jul 24;126(4):392-401. doi: 10.1161/CIRCULATIONAHA.111.075382. Epub 2012 Jun 18.

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