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Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Current cardiology reports, 2019-11, Vol.21 (12), p.155-155, Article 155

2019

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Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

Heart (British Cardiac Society), 2008-11, Vol.94 (11), p.1478-1484

2008

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Uncertain diagnosis of Fabry disease: Consensus recommendation on diagnosis in adults with left ventricular hypertrophy and genetic variants of unknown significance

International journal of cardiology, 2014-12, Vol.177 (2), p.400-408

2014

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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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Effects of enzyme replacement therapy on the cardiomyopathy of Anderson–Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa

Heart (British Cardiac Society), 2008-02, Vol.94 (2), p.153-158

2008

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Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy

Heart (British Cardiac Society), 2006-06, Vol.92 (6), p.785-791

2006

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Prevalence of exercise-induced left ventricular outflow tract obstruction in symptomatic patients with non-obstructive hypertrophic cardiomyopathy

Heart (British Cardiac Society), 2008-10, Vol.94 (10), p.1288-1294

2008

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Hypertrophic cardiomyopathy: the interrelation of disarray, fibrosis, and small vessel disease

British heart journal, 2000-11, Vol.84 (5), p.476-482

2000

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Coronary microvascular dysfunction in male patients with Anderson-Fabry disease and the effect of treatment with α galactosidase A

Heart (British Cardiac Society), 2006-03, Vol.92 (3), p.357-360

2006

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A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM Risk-SCD)

European heart journal, 2014-08, Vol.35 (30), p.2010-2020

2014

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Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases

European heart journal, 2013-05, Vol.34 (19), p.1448-1458

2013

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Left ventricular diastolic function assessed using Doppler tissue imaging in patients with hypertrophic cardiomyopathy: relation to symptoms and exercise capacity

British heart journal, 2002-03, Vol.87 (3), p.247-251

2002

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Quantitative SPECT/CT parameters of myocardial 99mTechnetium-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD) uptake in suspected cardiac transthyretin amyloidosis

EJNMMI research, 2021-09, Vol.11 (1), p.86-86, Article 86

2021

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Septal myotomy–myectomy and transcoronary septal alcohol ablation in hypertrophic obstructive cardiomyopathy. A comparison of clinical, haemodynamic and exercise outcomes

European heart journal, 2002-10, Vol.23 (20), p.1617-1624

2002

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Pregnancy related complications in women with hypertrophic cardiomyopathy

British heart journal, 2003-07, Vol.89 (7), p.752-756

2003

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Episodic syncope in hypertrophic cardiomyopathy: evidence for inappropriate vasodilation

Heart (British Cardiac Society), 2008-10, Vol.94 (10), p.1312-1317

2008

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Prevalence and clinical significance of systolic impairment in hypertrophic cardiomyopathy

Heart (British Cardiac Society), 2005-07, Vol.91 (7), p.920-925

2005

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The heart in Anderson-Fabry disease and other lysosomal storage disorders

Heart (British Cardiac Society), 2007-04, Vol.93 (4), p.528-535

2007

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Anderson-Fabry disease in heart failure

Biophysical reviews, 2018-08, Vol.10 (4), p.1107-1119

2018

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Loss‐of‐function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

British journal of dermatology (1951), 2019-05, Vol.180 (5), p.1114-1122

2019

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Myocardial late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy caused by mutations in troponin I

Heart (British Cardiac Society), 2005-08, Vol.91 (8), p.1036-1040

2005

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Prospective prognostic assessment of blood pressure response during exercise in patients with hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 1997-11, Vol.96 (9), p.2987-2991

1997

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B-type natriuretic peptide predicts disease severity in children with hypertrophic cardiomyopathy

Heart (British Cardiac Society), 2008-10, Vol.94 (10), p.1307-1311

2008

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Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

Uncertain diagnosis of Fabry disease: Consensus recommendation on diagnosis in adults with left ventricular hypertrophy and genetic variants of unknown significance

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

Effects of enzyme replacement therapy on the cardiomyopathy of Anderson–Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa

Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy

Prevalence of exercise-induced left ventricular outflow tract obstruction in symptomatic patients with non-obstructive hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy: the interrelation of disarray, fibrosis, and small vessel disease

Coronary microvascular dysfunction in male patients with Anderson-Fabry disease and the effect of treatment with α galactosidase A

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM Risk-SCD)

Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases

Left ventricular diastolic function assessed using Doppler tissue imaging in patients with hypertrophic cardiomyopathy: relation to symptoms and exercise capacity

Quantitative SPECT/CT parameters of myocardial 99mTechnetium-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD) uptake in suspected cardiac transthyretin amyloidosis

Septal myotomy–myectomy and transcoronary septal alcohol ablation in hypertrophic obstructive cardiomyopathy. A comparison of clinical, haemodynamic and exercise outcomes

Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Pregnancy related complications in women with hypertrophic cardiomyopathy

Episodic syncope in hypertrophic cardiomyopathy: evidence for inappropriate vasodilation

Prevalence and clinical significance of systolic impairment in hypertrophic cardiomyopathy

The heart in Anderson-Fabry disease and other lysosomal storage disorders

Anderson-Fabry disease in heart failure

Loss‐of‐function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

Myocardial late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy caused by mutations in troponin I

Prospective prognostic assessment of blood pressure response during exercise in patients with hypertrophic cardiomyopathy

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)

B-type natriuretic peptide predicts disease severity in children with hypertrophic cardiomyopathy

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