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The natural history of hypertrophic cardiomyopathy

European heart journal supplements, 2020-11, Vol.22 (Suppl L), p.L11-L14

2020

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Old and new therapeutic solutions in the treatment of hypertrophic cardiomyopathy

European heart journal supplements, 2023-04, Vol.25 (Supplement_B), p.B12-B15

2023

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Implantable cardioverter-defibrillators for hypertrophic cardiomyopathy: The Times They Are a-Changin

Europace (London, England), 2022-10, Vol.24 (9), p.1384-1394

2022

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Diagnostic delay in arrhythmogenic cardiomyopathy

European journal of preventive cardiology, 2023-09, Vol.30 (13), p.1315-1322

2023

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Clinical course of hypertrophic cardiomyopathy patients implanted with a transvenous or subcutaneous defibrillator

Europace (London, England), 2023-08, Vol.25 (9)

2023

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A national survey on prevalence of possible echocardiographic red flags of amyloid cardiomyopathy in consecutive patients undergoing routine echocardiography: study design and patients characterization - the first insight from the AC-TIVE Study

European journal of preventive cardiology, 2022-05, Vol.29 (5), p.e173-e177

2022

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Arrhythmic risk stratification in patients with left ventricular ring-like scar

European journal of preventive cardiology, 2024-11

2024

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1064 LONG QTC IN HCM: A CONSEQUENCE OF MYOCARDIAL HYPERTROPHY OR A DISTINCT GENETIC DISEASE?

European heart journal supplements, 2022-12, Vol.24 (Supplement_K)

2022

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Prognostic relevance of GRACE risk score in Takotsubo syndrome

European heart journal. Acute cardiovascular care, 2020-10, Vol.9 (7), p.721-728

2020

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310 CLINICAL COURSE AND CHARACTERISTICS OF ADVANCED HEART FAILURE ASSOCIATED WITH ARRHYTHMOGENIC CARDIOMYOPATHY

European heart journal supplements, 2022-12, Vol.24 (Supplement_K)

2022

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1041 ELECTROCARDIOGRAPHIC HETEROGENEITY OF PATIENTS WITH VARIANT TRANSTHYRETIN AMYLOID CARDIOMYOPATHY: GENOTYPE PHENOTYPE CORRELATIONS

European heart journal supplements, 2022-12, Vol.24 (Supplement_K)

2022

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Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA(Ile) mutation causing hypertrophic cardiomyopathy

Human molecular genetics, 2012-01, Vol.21 (1), p.85-100

2012

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370 The CO-existence of KCNQ1 and TNNI3 genes mutations supports the genetic origin of QTC abnormalities in hypertrophic cardiomyopathy

European heart journal supplements, 2020-12, Vol.22 (Supplement_N), p.N83-N87

2020

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53 Exercise oxygen kinetic in hypertrophic cardiomyopathy: results from a multicentre cardiopulmonary exercise testing study

European heart journal supplements, 2021-12, Vol.23 (Supplement_G)

2021

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Apical hypertrophic cardiomyopathy or left ventricular non-compaction? A difficult differential diagnosisThe opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology

European heart journal, 2007-08, Vol.28 (16), p.1923

2007

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Apical hypertrophic cardiomyopathy or left ventricular non-compaction? A difficult differential diagnosis The opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology

European heart journal, 2007-08, Vol.28 (16), p.1923-1924

2007

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QRS duration and QRS fractionation on surface electrocardiogram are markers of right ventricular dysfunction and atrialization in patients with Ebstein anomaly

European heart journal, 2013-01, Vol.34 (3), p.191-200

2013

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465 Unmasking the prevalence of cardiac amyloidosis in the real world: first insights from the phase 2 of active study, an Italian nationwide survey

European heart journal supplements, 2021-12, Vol.23 (Supplement_G)

2021

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Apical hypertrophic cardiomyopathy or left ventricular non-compaction? A difficult differential diagnosis

European heart journal, 2007-08, Vol.28 (16), p.1923-1924

2007

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'QRS duration and QRS fractionation on surface electrocardiogram are markers of right ventricular dysfunction and atrialization in patients with Ebstein anomaly' [Eur Heart J 2012;34:191-200, doi:10.1093/eurheartj/ehs362]

European heart journal, 2013-02, Vol.34 (8), p.624-624

2013

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Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA super(Ile) mutation causing hypertrophic cardiomyopathy

Human molecular genetics, 2012-01, Vol.21 (1), p.85-100

2012

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Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIle mutation causing hypertrophic cardiomyopathy

Human molecular genetics, 2012-01, Vol.21 (1), p.85-100

2012

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The natural history of hypertrophic cardiomyopathy

Old and new therapeutic solutions in the treatment of hypertrophic cardiomyopathy

Implantable cardioverter-defibrillators for hypertrophic cardiomyopathy: The Times They Are a-Changin

Diagnostic delay in arrhythmogenic cardiomyopathy

Clinical course of hypertrophic cardiomyopathy patients implanted with a transvenous or subcutaneous defibrillator

A national survey on prevalence of possible echocardiographic red flags of amyloid cardiomyopathy in consecutive patients undergoing routine echocardiography: study design and patients characterization - the first insight from the AC-TIVE Study

Arrhythmic risk stratification in patients with left ventricular ring-like scar

1064 LONG QTC IN HCM: A CONSEQUENCE OF MYOCARDIAL HYPERTROPHY OR A DISTINCT GENETIC DISEASE?

Prognostic relevance of GRACE risk score in Takotsubo syndrome

310 CLINICAL COURSE AND CHARACTERISTICS OF ADVANCED HEART FAILURE ASSOCIATED WITH ARRHYTHMOGENIC CARDIOMYOPATHY

1041 ELECTROCARDIOGRAPHIC HETEROGENEITY OF PATIENTS WITH VARIANT TRANSTHYRETIN AMYLOID CARDIOMYOPATHY: GENOTYPE PHENOTYPE CORRELATIONS

Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA(Ile) mutation causing hypertrophic cardiomyopathy

370 The CO-existence of KCNQ1 and TNNI3 genes mutations supports the genetic origin of QTC abnormalities in hypertrophic cardiomyopathy

53 Exercise oxygen kinetic in hypertrophic cardiomyopathy: results from a multicentre cardiopulmonary exercise testing study

Apical hypertrophic cardiomyopathy or left ventricular non-compaction? A difficult differential diagnosisThe opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology

Apical hypertrophic cardiomyopathy or left ventricular non-compaction? A difficult differential diagnosis The opinions expressed in this article are not necessarily those of the Editors of the European Heart Journal or of the European Society of Cardiology

QRS duration and QRS fractionation on surface electrocardiogram are markers of right ventricular dysfunction and atrialization in patients with Ebstein anomaly

465 Unmasking the prevalence of cardiac amyloidosis in the real world: first insights from the phase 2 of active study, an Italian nationwide survey

Apical hypertrophic cardiomyopathy or left ventricular non-compaction? A difficult differential diagnosis

'QRS duration and QRS fractionation on surface electrocardiogram are markers of right ventricular dysfunction and atrialization in patients with Ebstein anomaly' [Eur Heart J 2012;34:191-200, doi:10.1093/eurheartj/ehs362]

Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA super(Ile) mutation causing hypertrophic cardiomyopathy

Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIle mutation causing hypertrophic cardiomyopathy

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