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Beyond cholesterol metabolism: The pleiotropic effects of proprotein convertase subtilisin/kexin type 9 (PCSK9). Genetics, mutations, expression, and perspective for long‐term inhibition

BioFactors (Oxford), 2020-05, Vol.46 (3), p.367-380

2020

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Lipoprotein(a): a genetic marker for cardiovascular disease and target for emerging therapies

Journal of cardiovascular medicine (Hagerstown, Md.), 2021-03, Vol.22 (3), p.151-161

2021

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Desmosomes in heart and skin: friends or foes?

Journal of translational medicine, 2024-04, Vol.22 (1), p.357-357, Article 357

2024

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Molecular Basis of Inflammation in the Pathogenesis of Cardiomyopathies

International journal of molecular sciences, 2020-09, Vol.21 (18), p.6462

2020

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Hypertrophic Cardiomyopathy—Current Challenges and Future Perspectives

Journal of clinical medicine, 2023-09, Vol.12 (18), p.6093

2023

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The Hidden Fragility in the Heart of the Athletes: A Review of Genetic Biomarkers

International journal of molecular sciences, 2020-09, Vol.21 (18), p.6682

2020

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Athlete's Heart: A Cardiovascular Step-By-Step Multimodality Approach

Reviews in cardiovascular medicine, 2023-05, Vol.24 (5), p.151

2023

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Editorial: Cardiovascular genetics-focus on paediatric cardiomyopathy

Frontiers in pediatrics, 2023-02, Vol.11, p.1147527-1147527

2023

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The Expanding Spectrum of FLNC Cardiomyopathy

Cardiogenetics, 2022-11, Vol.12 (4), p.276-277

2022

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Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes

International journal of molecular sciences, 2023-05, Vol.24 (10), p.9108

2023

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Integrated Sudden Cardiac Death Risk Prediction Model For Patients With Hypertrophic Cardiomyopathy

Circulation (New York, N.Y.), 2023-01, Vol.147 (4), p.281-283

2023

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Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases

PloS one, 2020-05, Vol.15 (5), p.e0233050

2020

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Sudden cardiac death risk prediction in Fabry disease: How many strings do we have on our bow?

International journal of cardiology, 2025-01, Vol.418, p.132592, Article 132592

2025

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Hypertrophic Cardiomyopathy in Children: Pathophysiology, Diagnosis, and Treatment of Non-sarcomeric Causes

Frontiers in pediatrics, 2021-02, Vol.9, p.632293-632293

2021

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Letter by Monda and Limongelli Regarding Article, "The Prevalence and Association of Exercise Test Abnormalities With Sudden Cardiac Death and Transplant-Free Survival in Childhood Hypertrophic Cardiomyopathy"

Circulation (New York, N.Y.), 2023-07, Vol.148 (1), p.73-73

2023

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Editorial: Paediatric Cardiomyopathies

Frontiers in pediatrics, 2021-05, Vol.9, p.696443-696443

2021

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A Roadmap to Predict Adverse Outcome in Fabry Disease

Journal of the American College of Cardiology, 2022-09, Vol.80 (10), p.995-997

2022

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Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes

Biomolecules (Basel, Switzerland), 2022-10, Vol.12 (10), p.1417

2022

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Expanding the knowledge on transthyretin p. V142I variant‐related cardiomyopathy

European journal of heart failure, 2024-02, Vol.26 (2), p.394-396

2024

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Expanding the knowledge on transthyretin p.V142I variant‐related cardiomyopathy

European journal of heart failure, 2024-02, Vol.26 (2), p.394-396

2024

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Letter by Monda and Limongelli Regarding Article, “Changes in Cardiac Function Following Fulminant Myocarditis”

Circulation. Heart failure, 2024-09, Vol.17 (9)

2024

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Thromboembolic events in peripartum cardiomyopathy: Current dilemmas and future perspectives

European journal of heart failure, 2023-08, Vol.25 (8), p.1467-1469

2023

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An Overview of Molecular Mechanisms in Fabry Disease

Biomolecules (Basel, Switzerland), 2022-10, Vol.12 (10), p.1460

2022

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Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation

Genes, 2022-08, Vol.13 (9), p.1503

2022

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Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic Cardiomyopathy

Genes, 2020-08, Vol.11 (8), p.947

2020

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Beyond cholesterol metabolism: The pleiotropic effects of proprotein convertase subtilisin/kexin type 9 (PCSK9). Genetics, mutations, expression, and perspective for long‐term inhibition

Lipoprotein(a): a genetic marker for cardiovascular disease and target for emerging therapies

Desmosomes in heart and skin: friends or foes?

Molecular Basis of Inflammation in the Pathogenesis of Cardiomyopathies

Hypertrophic Cardiomyopathy—Current Challenges and Future Perspectives

The Hidden Fragility in the Heart of the Athletes: A Review of Genetic Biomarkers

Athlete's Heart: A Cardiovascular Step-By-Step Multimodality Approach

Editorial: Cardiovascular genetics-focus on paediatric cardiomyopathy

The Expanding Spectrum of FLNC Cardiomyopathy

Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes

Integrated Sudden Cardiac Death Risk Prediction Model For Patients With Hypertrophic Cardiomyopathy

Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases

Sudden cardiac death risk prediction in Fabry disease: How many strings do we have on our bow?

Hypertrophic Cardiomyopathy in Children: Pathophysiology, Diagnosis, and Treatment of Non-sarcomeric Causes

Letter by Monda and Limongelli Regarding Article, "The Prevalence and Association of Exercise Test Abnormalities With Sudden Cardiac Death and Transplant-Free Survival in Childhood Hypertrophic Cardiomyopathy"

Editorial: Paediatric Cardiomyopathies

A Roadmap to Predict Adverse Outcome in Fabry Disease

Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes

Expanding the knowledge on transthyretin p. V142I variant‐related cardiomyopathy

Expanding the knowledge on transthyretin p.V142I variant‐related cardiomyopathy

Letter by Monda and Limongelli Regarding Article, “Changes in Cardiac Function Following Fulminant Myocarditis”

Thromboembolic events in peripartum cardiomyopathy: Current dilemmas and future perspectives

An Overview of Molecular Mechanisms in Fabry Disease

Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation

Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic Cardiomyopathy

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