Eduardo
Villacorta Argüelles
Profesor Asociado CC. Salud
Publicaciones (50) Publicaciones de Eduardo Villacorta Argüelles
2024
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Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives
Journal of the American College of Cardiology, Vol. 83, Núm. 17, pp. 1640-1651
2023
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Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry
European Heart Journal - Quality of Care and Clinical Outcomes, Vol. 9, Núm. 1, pp. 42-53
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Burden of untreated transthyretin amyloid cardiomyopathy on patients and their caregivers by disease severity: results from a multicenter, non-interventional, real-world study
Frontiers in Cardiovascular Medicine, Vol. 10
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Heart failure in a patient with multiple myeloma
REC: CardioClinics, Vol. 58, Núm. 4, pp. 333-334
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Importance of genetic study in elderly patients with transthyretin cardiac amyloidosis
Medicina Clinica, Vol. 161, Núm. 9, pp. 382-385
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Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype-phenotype correlation
European heart journal. Cardiovascular Imaging, Vol. 25, Núm. 1, pp. 75-85
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Selection of the best of 2022 in familial heart disease and cardiovascular genetics
REC: CardioClinics, Vol. 58, pp. S68-S73
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Unravelling an hypertrophic myocardiopathy
European heart journal, Vol. 44, Núm. 29, pp. 2788
2022
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Combination of late gadolinium enhancement and genotype improves prediction of prognosis in non-ischaemic dilated cardiomyopathy
European Journal of Heart Failure, Vol. 24, Núm. 7, pp. 1183-1196
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Drug-eluting stents and contemporary dual antiplatelet therapy in revascularized STEMI. The times they are a-changin’?
Revista Espanola de Cardiologia, Vol. 75, Núm. 8, pp. 623-625
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Impact of SARS-Cov-2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry
ESC Heart Failure, Vol. 9, Núm. 4, pp. 2189-2198
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Natural History of MYH7-Related Dilated Cardiomyopathy
Journal of the American College of Cardiology, Vol. 80, Núm. 15, pp. 1447-1461
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Pericardial and myocardial involvement after SARS-CoV-2 infection: a cross-sectional descriptive study in healthcare workers
Revista Espanola de Cardiologia, Vol. 75, Núm. 9, pp. 735-747
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Selection of the best of 2021 in familial heart disease and cardiovascular genetics
REC: CardioClinics, Vol. 57, pp. S54-S59
2021
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A rare HCN4 variant with combined sinus bradycardia, left atrial dilatation, and hypertrabeculation/left ventricular noncompaction phenotype
Revista Espanola de Cardiologia, Vol. 74, Núm. 9, pp. 781-789
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Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy
European Heart Journal, Vol. 42, Núm. 32, pp. 3063-3073
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Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy
Journal of the American College of Cardiology, Vol. 78, Núm. 17, pp. 1682-1699
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COVID-19 Outbreak Resources Optimization: Rapid Adaptation of a Catheterization Laboratory Into a New Intensive Cardiac Care Unit
The Journal of cardiovascular nursing, Vol. 36, Núm. 1, pp. 88-90
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Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction
Journal of the American College of Cardiology, Vol. 78, Núm. 7, pp. 643-662
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Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry
ESC Heart Failure, Vol. 8, Núm. 1, pp. 95-105