Cardiopatías Familiares y genética cardiovascular
Policlinico S.Orsola-Malpighi
Bolonia, ItaliaPublicaciones en colaboración con investigadores/as de Policlinico S.Orsola-Malpighi (10)
2024
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A cost-effectiveness analysis of hypertrophic cardiomyopathy sudden cardiac death risk algorithms for implantable cardioverter defibrillator decision-making
European Heart Journal - Quality of Care and Clinical Outcomes, Vol. 10, Núm. 4, pp. 285-293
2022
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Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic Cardiomyopathy
Journal of the American College of Cardiology, Vol. 79, Núm. 20, pp. 1986-1997
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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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Relationship Between Maximal Left Ventricular Wall Thickness and Sudden Cardiac Death in Childhood Onset Hypertrophic Cardiomyopathy
Circulation. Arrhythmia and electrophysiology, Vol. 15, Núm. 5, pp. e010075
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The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy
European Journal of Preventive Cardiology, Vol. 29, Núm. 4, pp. 645-653
2021
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Current use of cardiac magnetic resonance in tertiary referral centres for the diagnosis of cardiomyopathy: The ESC EORP Cardiomyopathy/Myocarditis Registry
European Heart Journal Cardiovascular Imaging, Vol. 22, Núm. 7, pp. 781-789
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Prospective follow-up in various subtypes of cardiomyopathies: Insights from the ESC EORP Cardiomyopathy Registry
European Heart Journal - Quality of Care and Clinical Outcomes, Vol. 7, Núm. 2, pp. 134-142
2020
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Clinical Profile of Cardiac Involvement in Danon Disease: A Multicenter European Registry
Circulation: Genomic and Precision Medicine, Vol. 13, Núm. 6, pp. E003117
2019
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Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)
JAMA Cardiology, Vol. 4, Núm. 9, pp. 918-927