Cardioloxía
Servizo
Vall d'Hebron Institut de Recerca
Barcelona, EspañaPublicacións en colaboración con investigadores/as de Vall d'Hebron Institut de Recerca (29)
2024
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Prognostic Utility of Society for Cardiovascular Angiography and Interventions Shock Stage Approach for Classifying Cardiogenic Shock Severity in Takotsubo Syndrome
Journal of the American Heart Association, Vol. 13, Núm. 6, pp. e032951
2023
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Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure
European Heart Journal, Vol. 44, Núm. 48, pp. 5064-5073
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Heart rate disorders in patients with Tako-tsubo syndrome
Medicina Clinica, Vol. 161, Núm. 8, pp. 330-337
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Impact of dapagliflozin on cardiac remodelling in patients with chronic heart failure: The DAPA-MODA study
European Journal of Heart Failure, Vol. 25, Núm. 8, pp. 1352-1360
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Mechanical circulatory support in severe primary graft dysfunction: Peripheral cannulation but not earlier implantation improves survival in heart transplantation
Journal of Heart and Lung Transplantation, Vol. 42, Núm. 8, pp. 1101-1111
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Post-COVID-19 syndrome and diabetes mellitus: a propensity-matched analysis of the International HOPE-II COVID-19 Registry
Frontiers in Endocrinology, Vol. 14
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Safety and Efficacy of TAVR With a Pressure Sensor and Pacing Guidewire: SAFE-TAVI Trial
JACC: Cardiovascular Interventions, Vol. 16, Núm. 24, pp. 3016-3023
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Selection of the best of 2022 in cardiac imaging
REC: CardioClinics, Vol. 58, pp. S28-S34
2022
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Aortic flow dynamics and stiffness in Loeys-Dietz syndrome patients: a comparison with healthy volunteers and Marfan syndrome patients
European heart journal. Cardiovascular Imaging, Vol. 23, Núm. 5, pp. 641-649
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Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study
European Journal of Medical Genetics, Vol. 65, Núm. 6
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Characterization of hereditary transthyretin cardiac amyloidosis in Spain
Revista Espanola de Cardiologia, Vol. 75, Núm. 6, pp. 488-495
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Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy
Journal of the American College of Cardiology, Vol. 80, Núm. 12, pp. 1115-1126
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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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Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator
European heart journal, Vol. 43, Núm. 32, pp. 3053-3067
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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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Unraveling Bicuspid Aortic Valve Enigmas by Multimodality Imaging: Clinical Implications
Journal of Clinical Medicine, Vol. 11, Núm. 2
2021
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Aortic Branch Aneurysms and Vascular Risk in Patients With Marfan Syndrome
Journal of the American College of Cardiology, Vol. 77, Núm. 24, pp. 3005-3012
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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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Association of Left Ventricular Systolic Dysfunction among Carriers of Truncating Variants in Filamin C with Frequent Ventricular Arrhythmia and End-stage Heart Failure
JAMA Cardiology, Vol. 6, Núm. 8, pp. 891-901
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Changes in the diagnosis and management of acute aortic syndrome and associated mortality in the last 20 years
Revista Espanola de Cardiologia, Vol. 74, Núm. 3, pp. 257-262