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Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives

Circulation (New York, N.Y.), 2019-07, Vol.140 (3), p.184-192

2019

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A review of thoracic aortic aneurysm disease

Echo research and practice, 2020-03, Vol.7 (1), p.R1-R10

2020

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A social-healthcare pathway to facilitate return to work of cancer survivors in Italy: The UNAMANO project

Work (Reading, Mass.), 2021-01, Vol.70 (4), p.1243-1253

2021

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Looks Do Matter! Aortic Arch Shape After Hypoplastic Left Heart Syndrome Palliation Correlates With Cavopulmonary Outcomes

The Annals of thoracic surgery, 2017-02, Vol.103 (2), p.645-654

2017

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Cardiac Manifestations of Myotonic Dystrophy in a Pediatric Cohort

Frontiers in pediatrics, 2022-06, Vol.10, p.910660-910660

2022

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Interventricular Delay Interval Optimization in Cardiac Resynchronization Therapy Guided by Echocardiography Versus Guided by Electrocardiographic QRS Interval Width

The American journal of cardiology, 2008-11, Vol.102 (10), p.1373-1377

2008

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Childhood-onset hypertrophic cardiomyopathy caused by thin-filament sarcomeric variants

Journal of medical genetics, 2024-05, Vol.61 (5), p.420-422

2024

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Asymptomatic adults with mild/moderate isolated native pulmonary valve stenosis are in need of treatment… but not the kind you are thinking of

Heart (British Cardiac Society), 2014-09, Vol.100 (17), p.1313-1314

2014

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Clinical Management of Atrial Fibrillation

Chest, 2011-10, Vol.140 (4), p.843-845

2011

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Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives: Evidence for a Change in Paradigm

Circulation (New York, N.Y.), 2019-07, Vol.140 (3), p.184-192

2019

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Are aortic biomechanical properties early markers of dilatation in patients with Marfan syndrome? A systematic review and meta-analysis

Biomechanics and modeling in mechanobiology, 2024-12, Vol.23 (6), p.2043-2061

2024

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7 Relation between N-terminal pro B-type natriuretic peptide (NT-probnp) and disease severity in paediatric hypertrophic cardiomyopathy

Heart (British Cardiac Society), 2021-06, Vol.107 (Suppl 1), p.A6-A6

2021

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Utility and acceptability of remote 6-lead electrocardiographic monitoring in children with inherited cardiac conditions

Archives of disease in childhood, 2024-09, Vol.109 (9), p.742-747

2024

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Disopyramide is a safe and effective treatment for children with obstructive hypertrophic cardiomyopathy

International journal of cardiology, 2023-01, Vol.371, p.523-525

2023

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Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease

Journal of the American College of Cardiology, 2022-08, Vol.80 (9), p.857-869

2022

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Management of aortic disease in children with FBN1-related Marfan syndrome: A joint statement from the paediatric subgroup of the European Reference Network of Vascular Diseases (VASCERN, Heritable Thoracic Aortic Disease working group) and the Association for European Paediatric and Congenital Cardiology (AEPC)

European heart journal, 2024-09, Vol.45 (39), p.4156-4169

2024

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Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial

The Lancet (British edition), 2019-12, Vol.394 (10216), p.2263-2270

2019

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Performance of the PRIMaCY sudden death risk prediction model for childhood hypertrophic cardiomyopathy: implications for implantable cardioverter-defibrillator decision-making

Europace (London, England), 2023-11, Vol.25 (11)

2023

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Arterial tortuosity in pediatric Loeys‐Dietz syndrome patients

American journal of medical genetics. Part A, 2024-03, Vol.194 (3), p.e63465-n/a

2024

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Management of aortic disease in children with FBN1-related Marfan syndrome

European heart journal, 2024-10, Vol.45 (39), p.4156-4169

2024

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Friedreich’s ataxia-associated childhood hypertrophic cardiomyopathy: a national cohort study

Archives of disease in childhood, 2022-05, Vol.107 (5), p.450-455

2022

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External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy

European journal of preventive cardiology, 2022-03, Vol.29 (4), p.678-686

2022

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Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes

Journal of medical genetics, 2022-08, Vol.59 (8), p.768-775

2022

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Mathematical modelling of the maternal cardiovascular system in the three stages of pregnancy

Medical engineering & physics, 2017-09, Vol.47, p.55-63

2017

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Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives

A review of thoracic aortic aneurysm disease

A social-healthcare pathway to facilitate return to work of cancer survivors in Italy: The UNAMANO project

Looks Do Matter! Aortic Arch Shape After Hypoplastic Left Heart Syndrome Palliation Correlates With Cavopulmonary Outcomes

Clinical presentation and long‐term outcomes of infantile hypertrophic cardiomyopathy: a European multicentre study

Cardiac Manifestations of Myotonic Dystrophy in a Pediatric Cohort

Interventricular Delay Interval Optimization in Cardiac Resynchronization Therapy Guided by Echocardiography Versus Guided by Electrocardiographic QRS Interval Width

Childhood-onset hypertrophic cardiomyopathy caused by thin-filament sarcomeric variants

Asymptomatic adults with mild/moderate isolated native pulmonary valve stenosis are in need of treatment… but not the kind you are thinking of

Clinical Management of Atrial Fibrillation

Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives: Evidence for a Change in Paradigm

Are aortic biomechanical properties early markers of dilatation in patients with Marfan syndrome? A systematic review and meta-analysis

7 Relation between N-terminal pro B-type natriuretic peptide (NT-probnp) and disease severity in paediatric hypertrophic cardiomyopathy

Utility and acceptability of remote 6-lead electrocardiographic monitoring in children with inherited cardiac conditions

Disopyramide is a safe and effective treatment for children with obstructive hypertrophic cardiomyopathy

Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease

Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial

Performance of the PRIMaCY sudden death risk prediction model for childhood hypertrophic cardiomyopathy: implications for implantable cardioverter-defibrillator decision-making

Arterial tortuosity in pediatric Loeys‐Dietz syndrome patients

Management of aortic disease in children with FBN1-related Marfan syndrome

Friedreich’s ataxia-associated childhood hypertrophic cardiomyopathy: a national cohort study

External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy

Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes

Mathematical modelling of the maternal cardiovascular system in the three stages of pregnancy

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