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Programmed Ventricular Stimulation as an Additional Primary Prevention Risk Stratification Tool in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Study

Circulation (New York, N.Y.), 2022-11, Vol.146 (19), p.1434-1443

2022

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Ventricular arrhythmias in arrhythmic mitral valve syndrome-a prospective continuous long-term cardiac monitoring study

Europace (London, England), 2023-02, Vol.25 (2), p.506-516

2023

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Highly malignant disease in childhood-onset arrhythmogenic right ventricular cardiomyopathy

European heart journal, 2022-12, Vol.43 (45), p.4694-4703

2022

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Electrical markers and arrhythmic risk associated with myocardial fibrosis in mitral valve prolapse

Europace (London, England), 2022-07, Vol.24 (7), p.1156-1163

2022

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Lamin A/C cardiomyopathy in children

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Flecainide in patients with arrhythmic mitral valve syndrome: A case series

Heart rhythm, 2023-04, Vol.20 (4), p.635-636

2023

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Highly malignant disease in early-onset arrhythmogenic cardiomyopathy

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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Progression of cardiac disease in patients with lamin A/C mutations

European heart journal cardiovascular imaging, 2022-03, Vol.23 (4), p.543-550

2022

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Non-sustained ventricular arrhythmias at exercise ECG predict severe ventricular arrhythmias in arrhythmic mitral valve prolapse

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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1175Structural progression increases the risk of ventricular arrhythmias in patients with arrhythmogenic cardiomyopathy

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

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Exercise-induced troponin I elevation is associated with alterations in regional longitudinal strain

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Disease progression rate is a strong predictor of ventricular arrhythmias in patients with cardiac laminopathies: a primary prevention cohort study

Europace (London, England), 2023-02, Vol.25 (2), p.634-642

2023

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Timing of cardioverter-defibrillator implantation in patients with cardiac laminopathies—External validation of the LMNA-risk ventricular tachyarrhythmia calculator

Heart rhythm, 2023-03, Vol.20 (3), p.423-429

2023

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Predictors of ventricular arrhythmias in arrhythmic mitral valve syndrome – a study using implantable loop recorders

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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Echocardiographic parameters of myocardial work in relation to prolonged strenuous physical exercise

European heart journal, 2021-10, Vol.42 (Supplement_1)

2021

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Mitral annulus disjunction is highly prevalent in patients with Marfan syndrome and Loyes-Dietz syndrome

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Threshold values by electrocardiogram and echocardiography indicating transition to an arrhythmic phenotype in cardiac laminopathies: a primary prevention cohort study

Europace (London, England), 2022-05, Vol.24 (Supplement_1)

2022

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Novel echocardiographic measures of myocardial work predicts physical performance during prolonged strenuous exercise

European journal of preventive cardiology, 2022-05, Vol.29 (Supplement_1)

2022

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Sex differences in disease progression and arrhythmic risk in patients with arrhythmogenic cardiomyopathy

European heart journal cardiovascular imaging, 2021-02, Vol.22 (Supplement_1)

2021

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P1804 Phenotypic overlap between Brugada syndrome and arrhythmogenic cardiomyopathy

European heart journal cardiovascular imaging, 2020-01, Vol.21 (Supplement_1)

2020

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Mitral annulus disjunction is associated with adverse outcome in patients with Marfan syndrome and Loeys-Dietz syndrome

European heart journal cardiovascular imaging, 2021-02, Vol.22 (Supplement_1)

2021

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Quality of life determinants inpatients with hypertrophic cardiomyopathy and heart failure

Archives of Cardiovascular Diseases Supplements, 2018-01, Vol.10 (1), p.30-30

2018

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Left ventricular systolic function decreases in lamin a/c cardiomyopathy wihout concomitant ventricular dilatation

European heart journal cardiovascular imaging, 2021-02, Vol.22 (Supplement_1)

2021

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Romanian hypertrophic cardiomyopathy registry: Profile of patients included between 2014–2017

Archives of Cardiovascular Diseases Supplements, 2018-01, Vol.10 (1), p.37-38

2018

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Toward stomatal–flux based forest protection against ozone: The MOTTLES approach

The Science of the total environment, 2019-11, Vol.691, p.516-527

2019

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Programmed Ventricular Stimulation as an Additional Primary Prevention Risk Stratification Tool in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Study

Ventricular arrhythmias in arrhythmic mitral valve syndrome-a prospective continuous long-term cardiac monitoring study

Highly malignant disease in childhood-onset arrhythmogenic right ventricular cardiomyopathy

Electrical markers and arrhythmic risk associated with myocardial fibrosis in mitral valve prolapse

Lamin A/C cardiomyopathy in children

Flecainide in patients with arrhythmic mitral valve syndrome: A case series

Highly malignant disease in early-onset arrhythmogenic cardiomyopathy

Progression of cardiac disease in patients with lamin A/C mutations

Non-sustained ventricular arrhythmias at exercise ECG predict severe ventricular arrhythmias in arrhythmic mitral valve prolapse

1175Structural progression increases the risk of ventricular arrhythmias in patients with arrhythmogenic cardiomyopathy

Exercise-induced troponin I elevation is associated with alterations in regional longitudinal strain

Disease progression rate is a strong predictor of ventricular arrhythmias in patients with cardiac laminopathies: a primary prevention cohort study

Timing of cardioverter-defibrillator implantation in patients with cardiac laminopathies—External validation of the LMNA-risk ventricular tachyarrhythmia calculator

Predictors of ventricular arrhythmias in arrhythmic mitral valve syndrome – a study using implantable loop recorders

Echocardiographic parameters of myocardial work in relation to prolonged strenuous physical exercise

Mitral annulus disjunction is highly prevalent in patients with Marfan syndrome and Loyes-Dietz syndrome

Threshold values by electrocardiogram and echocardiography indicating transition to an arrhythmic phenotype in cardiac laminopathies: a primary prevention cohort study

Novel echocardiographic measures of myocardial work predicts physical performance during prolonged strenuous exercise

Sex differences in disease progression and arrhythmic risk in patients with arrhythmogenic cardiomyopathy

P1804 Phenotypic overlap between Brugada syndrome and arrhythmogenic cardiomyopathy

Mitral annulus disjunction is associated with adverse outcome in patients with Marfan syndrome and Loeys-Dietz syndrome

Quality of life determinants inpatients with hypertrophic cardiomyopathy and heart failure

Left ventricular systolic function decreases in lamin a/c cardiomyopathy wihout concomitant ventricular dilatation

Romanian hypertrophic cardiomyopathy registry: Profile of patients included between 2014–2017

Toward stomatal–flux based forest protection against ozone: The MOTTLES approach

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