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Contemporary Natural History and Management of Nonobstructive Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2016-03, Vol.67 (12), p.1399-1409

2016

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Obesity and its Association to Phenotype and Clinical Course in Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2013-07, Vol.62 (5), p.449-457

2013

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Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations

Journal of the American College of Cardiology, 2014-12, Vol.64 (24), p.2589-2600

2014

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Recurrent Intra-Stent Coronary Restenosis in a Carrier of Non-Disease-Specific Antinuclear Antibodies

European journal of case reports in internal medicine, 2024, Vol.11 (5), p.004412-004412

2024

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Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy

Circulation. Cardiovascular imaging, 2017-02, Vol.10 (2)

2017

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Prognostic Value of N-Terminal Pro-Brain Natriuretic Peptide in Outpatients With Hypertrophic Cardiomyopathy

The American journal of cardiology, 2013-10, Vol.112 (8), p.1190-1196

2013

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Comprehensive Risk Management in Arrhythmogenic Cardiomyopathy Associated With Autosomal Dominant Carvajal Syndrome

JACC. Case reports, 2020-06, Vol.2 (6), p.925-929

2020

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Atrial fibrillation and its influence on stroke risk

Research reports in clinical cardiology, 2015-01, Vol.6 (default), p.11-15

2015

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Peripheral artery disease and amputations with Sodium-Glucose co-Transporter-2 (SGLT-2) inhibitors: A meta-analysis of randomized controlled trials

Diabetes research and clinical practice, 2019-07, Vol.153, p.138-144

2019

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Anderson-Fabry, the Histrionic Disease: From Genetics to Clinical Management

Cardiogenetics, 2013-02, Vol.3 (11), p.e3-e3

2013

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Resurrection of a New Old Technique: Rotational Atherectomy

Circulation. Cardiovascular interventions, 2018-11, Vol.11 (11), p.e007421-e007421

2018

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Clinical Course and Significance of Hypertrophic Cardiomyopathy Without Left Ventricular Hypertrophy

Circulation (New York, N.Y.), 2019-02, Vol.139 (6), p.830-833

2019

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Intravascular lithotripsy for calcific coronary and peripheral artery stenoses

EuroIntervention, 2019-10, Vol.15 (8), p.714-721

2019

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Clinical and molecular classification of cardiomyopathies

Global Cardiology Science & Practice, 2012-07, Vol.2012 (1), p.4-4

2012

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Early Diagnosis and Outcome in Patients With Wild-Type Transthyretin Cardiac Amyloidosis

Mayo Clinic proceedings, 2021-08, Vol.96 (8), p.2185-2191

2021

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Comparison of long‐term outcome in anthracycline‐related versus idiopathic dilated cardiomyopathy: a single centre experience

European journal of heart failure, 2018-05, Vol.20 (5), p.898-906

2018

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Efficacy of Ranolazine in Patients With Symptomatic Hypertrophic Cardiomyopathy: The RESTYLE-HCM Randomized, Double-Blind, Placebo-Controlled Study

Circulation. Heart failure, 2018-01, Vol.11 (1), p.e004124-e004124

2018

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Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications

Journal of cardiovascular medicine (Hagerstown, Md.), 2018-01, Vol.19 (1), p.1-11

2018

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Defining phenotypes and disease progression in sarcomeric cardiomyopathies: contemporary role of clinical investigations

Cardiovascular research, 2015-04, Vol.105 (4), p.409-423

2015

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Pathophysiology and Treatment of Hypertrophic Cardiomyopathy: New Perspectives

Current heart failure reports, 2021-08, Vol.18 (4), p.169-179

2021

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Coronary microvascular dysfunction is an early feature of cardiac involvement in patients with Anderson-Fabry disease

European journal of heart failure, 2013-12, Vol.15 (12), p.1363-1373

2013

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Prevalence of Inherited Cardiac Diseases Among Young Patients Requiring Permanent Pacing

Circulation. Arrhythmia and electrophysiology, 2021-12, Vol.14 (12), p.e010562-e010562

2021

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Timing of invasive septal reduction therapies and outcome of patients with obstructive hypertrophic cardiomyopathy

International journal of cardiology, 2018-12, Vol.273, p.155-161

2018

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Contemporary Natural History and Management of Nonobstructive Hypertrophic Cardiomyopathy

Obesity and its Association to Phenotype and Clinical Course in Hypertrophic Cardiomyopathy

Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations

Recurrent Intra-Stent Coronary Restenosis in a Carrier of Non-Disease-Specific Antinuclear Antibodies

Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy

Significance of Late Gadolinium Enhancement at Right Ventricular Attachment to Ventricular Septum in Patients With Hypertrophic Cardiomyopathy

Prognostic Value of N-Terminal Pro-Brain Natriuretic Peptide in Outpatients With Hypertrophic Cardiomyopathy

Comprehensive Risk Management in Arrhythmogenic Cardiomyopathy Associated With Autosomal Dominant Carvajal Syndrome

Atrial fibrillation and its influence on stroke risk

Prognostic Value of Quantitative Contrast-Enhanced Cardiovascular Magnetic Resonance for the Evaluation of Sudden Death Risk in Patients With Hypertrophic Cardiomyopathy

Peripheral artery disease and amputations with Sodium-Glucose co-Transporter-2 (SGLT-2) inhibitors: A meta-analysis of randomized controlled trials

Anderson-Fabry, the Histrionic Disease: From Genetics to Clinical Management

Resurrection of a New Old Technique: Rotational Atherectomy

Clinical Course and Significance of Hypertrophic Cardiomyopathy Without Left Ventricular Hypertrophy

Intravascular lithotripsy for calcific coronary and peripheral artery stenoses

Clinical and molecular classification of cardiomyopathies

Early Diagnosis and Outcome in Patients With Wild-Type Transthyretin Cardiac Amyloidosis

Comparison of long‐term outcome in anthracycline‐related versus idiopathic dilated cardiomyopathy: a single centre experience

Efficacy of Ranolazine in Patients With Symptomatic Hypertrophic Cardiomyopathy: The RESTYLE-HCM Randomized, Double-Blind, Placebo-Controlled Study

Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications

Defining phenotypes and disease progression in sarcomeric cardiomyopathies: contemporary role of clinical investigations

Pathophysiology and Treatment of Hypertrophic Cardiomyopathy: New Perspectives

Coronary microvascular dysfunction is an early feature of cardiac involvement in patients with Anderson-Fabry disease

Prevalence of Inherited Cardiac Diseases Among Young Patients Requiring Permanent Pacing

Timing of invasive septal reduction therapies and outcome of patients with obstructive hypertrophic cardiomyopathy

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