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Circulating cardiac autoantibodies in dilated cardiomyopathy and myocarditis: pathogenetic and clinical significance

European journal of heart failure, 2002-08, Vol.4 (4), p.411-417

2002

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The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43

Clinical genetics, 2013-04, Vol.83 (4), p.321-331

2013

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Hypertrophic cardiomyopathy

The Lancet (British edition), 2004-06, Vol.363 (9424), p.1881-1891

2004

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Differentiation of heart failure related to dilated cardiomyopathy and coronary artery disease using gadolinium-enhanced cardiovascular magnetic resonance

Circulation (New York, N.Y.), 2003-07, Vol.108 (1), p.54-59

2003

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Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients

Journal of the American College of Cardiology, 2003-09, Vol.42 (5), p.873-879

2003

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Nuevas estrategias para evaluar la efectividad de servicios de insuficiencia cardiaca

Revista española de cardiologia, 2020-03, Vol.73 (3), p.200-204

2020

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Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 2002-03, Vol.105 (12), p.1407-1411

2002

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Cardiovascular pre-participation screening of young competitive athletes for prevention of sudden death : proposal for a common European protocol : Consensus Statement of the Study Group of Sport Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group of Myocardial and Pericardial Diseases of the European Society of Cardiology

European heart journal, 2005-03, Vol.26 (5), p.516-524

2005

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Toward clinical risk assessment in hypertrophic cardiomyopathy with gadolinium cardiovascular magnetic resonance

Journal of the American College of Cardiology, 2003-05, Vol.41 (9), p.1561-1567

2003

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Detection of apical hypertrophic cardiomyopathy by cardiovascular magnetic resonance in patients with non-diagnostic echocardiography

British heart journal, 2004-06, Vol.90 (6), p.645-649

2004

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Multicenter study of the efficacy and safety of disopyramide in obstructive hypertrophic cardiomyopathy

Journal of the American College of Cardiology, 2005-04, Vol.45 (8), p.1251-1258

2005

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Natural history and familial characteristics of isolated left ventricular non-compaction

European heart journal, 2005-01, Vol.26 (2), p.187-192

2005

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Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy

Circulation (New York, N.Y.), 2005-08, Vol.112 (5), p.636-642

2005

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Gadolinium enhanced cardiovascular magnetic resonance in Anderson-Fabry disease. Evidence for a disease specific abnormality of the myocardial interstitium

European heart journal, 2003-12, Vol.24 (23), p.2151

2003

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Sudden death in hypertrophic cardiomyopathy: identification of high risk patients

Journal of the American College of Cardiology, 2000-12, Vol.36 (7), p.2212-2218

2000

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Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)

The Lancet (British edition), 2000-06, Vol.355 (9221), p.2119-2124

2000

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Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

The Journal of clinical investigation, 2003-01, Vol.111 (2), p.209-216

2003

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Genetics of Right Ventricular Cardiomyopathy

Journal of cardiovascular electrophysiology, 2005-08, Vol.16 (8), p.927-935

2005

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American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy: A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines

European heart journal, 2003-11, Vol.24 (21), p.1965-1991

2003

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Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

Circulation (New York, N.Y.), 2006-01, Vol.113 (3), p.356-364

2006

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Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

Journal of the American College of Cardiology, 2004-11, Vol.44 (10), p.2033-2040

2004

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Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy

Journal of the American College of Cardiology, 2003-05, Vol.41 (10), p.1776-1782

2003

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New insights into the pathology of inherited cardiomyopathy

Heart (British Cardiac Society), 2005-02, Vol.91 (2), p.257-264

2005

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2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC)

Circulating cardiac autoantibodies in dilated cardiomyopathy and myocarditis: pathogenetic and clinical significance

The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43

Hypertrophic cardiomyopathy

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants

Differentiation of heart failure related to dilated cardiomyopathy and coronary artery disease using gadolinium-enhanced cardiovascular magnetic resonance

Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients

Nuevas estrategias para evaluar la efectividad de servicios de insuficiencia cardiaca

Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy

Toward clinical risk assessment in hypertrophic cardiomyopathy with gadolinium cardiovascular magnetic resonance

Detection of apical hypertrophic cardiomyopathy by cardiovascular magnetic resonance in patients with non-diagnostic echocardiography

Multicenter study of the efficacy and safety of disopyramide in obstructive hypertrophic cardiomyopathy

Natural history and familial characteristics of isolated left ventricular non-compaction

Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy

Gadolinium enhanced cardiovascular magnetic resonance in Anderson-Fabry disease. Evidence for a disease specific abnormality of the myocardial interstitium

Sudden death in hypertrophic cardiomyopathy: identification of high risk patients

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

Genetics of Right Ventricular Cardiomyopathy

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy

New insights into the pathology of inherited cardiomyopathy

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