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Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results

International journal of cardiology, 2017-10, Vol.245, p.92-98

2017

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Childhood Hypertrophic Cardiomyopathy: A Disease of the Cardiac Sarcomere

Frontiers in pediatrics, 2021-07, Vol.9, p.708679-708679

2021

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Racial Variation in Echocardiographic Reference Ranges for Left Chamber Dimensions in Children and Adolescents: A Systematic Review

Pediatric cardiology, 2018-06, Vol.39 (5), p.859-868

2018

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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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Long-term Safety and Efficacy of Mexiletine for Patients With Skeletal Muscle Channelopathies

JAMA neurology, 2015-12, Vol.72 (12), p.1531

2015

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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

2022

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Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)

The journal of clinical endocrinology and metabolism, 2014-08, Vol.99 (8), p.E1556-E1563

2014

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Proinflammatory and cardiovascular biomarkers are associated with echocardiographic abnormalities in children with HIV taking antiretroviral therapy

AIDS (London), 2022-12, Vol.36 (15), p.2129-2137

2022

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High prevalence of echocardiographic abnormalities in older HIV-infected children taking antiretroviral therapy

AIDS (London), 2018-11, Vol.32 (18), p.2739-2748

2018

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Echocardiographic reference ranges in older children and adolescents in sub-Saharan Africa

International journal of cardiology, 2017-12, Vol.248, p.409-413

2017

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Cardiac Disease in Adolescents With Delayed Diagnosis of Vertically Acquired HIV Infection

Clinical infectious diseases, 2013-02, Vol.56 (4), p.576-582

2013

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Value of Stress Transesophageal Echocardiography in an Asymptomatic Patient With Single Coronary Artery From Noncoronary Sinus, Intramural Course, and Ostial Stenosis

Circulation. Cardiovascular imaging, 2019-12, Vol.12 (1), p.e008560-e008560

2019

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Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype

Brain (London, England : 1878), 2015-10, Vol.138 (Pt 10), p.2859-2874

2015

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Prospective follow-up in various subtypes of cardiomyopathies: insights from the ESC EORP Cardiomyopathy Registry

European heart journal. Quality of care & clinical outcomes, 2021-04, Vol.7 (2), p.134-142

2021

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Nomenclature and systems of classification for cardiomyopathy in children

Cardiology in the young, 2015-08, Vol.25 (S2), p.31-42

2015

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Increased left ventricular posterior wall end-diastolic thickness in adolescents with delayed diagnosis of vertically acquired HIV infection

Journal of acquired immune deficiency syndromes (1999), 2014-08, Vol.66 (4), p.e90

2014

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Psychosocial adjustment and quality of life in children undergoing screening in a specialist paediatric hypertrophic cardiomyopathy clinic

Cardiology in the young, 2016-06, Vol.26 (5), p.961-967

2016

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Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

European heart journal, 2019-09, Vol.40 (35), p.2964-2975

2019

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Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

European heart journal, 2023-09, Vol.44 (35), p.3357-3370

2023

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Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

JAMA cardiology, 2019-09, Vol.4 (9), p.918

2019

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The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

European journal of preventive cardiology, 2022-03, Vol.29 (4), p.645

2022

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Cardiac phenotype in ATP1A3 -related syndromes: A multicenter cohort study

Neurology, 2020-11, Vol.95 (21), p.e2866

2020

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Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results

Childhood Hypertrophic Cardiomyopathy: A Disease of the Cardiac Sarcomere

Racial Variation in Echocardiographic Reference Ranges for Left Chamber Dimensions in Children and Adolescents: A Systematic Review

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

Long-term Safety and Efficacy of Mexiletine for Patients With Skeletal Muscle Channelopathies

Endomyocardial biopsy: safety and prognostic utility in paediatric and adult myocarditis in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Long-Term Registry

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

Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)

Proinflammatory and cardiovascular biomarkers are associated with echocardiographic abnormalities in children with HIV taking antiretroviral therapy

Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results

High prevalence of echocardiographic abnormalities in older HIV-infected children taking antiretroviral therapy

Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study

Echocardiographic reference ranges in older children and adolescents in sub-Saharan Africa

Cardiac Disease in Adolescents With Delayed Diagnosis of Vertically Acquired HIV Infection

Value of Stress Transesophageal Echocardiography in an Asymptomatic Patient With Single Coronary Artery From Noncoronary Sinus, Intramural Course, and Ostial Stenosis

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype

Prospective follow-up in various subtypes of cardiomyopathies: insights from the ESC EORP Cardiomyopathy Registry

Nomenclature and systems of classification for cardiomyopathy in children

Increased left ventricular posterior wall end-diastolic thickness in adolescents with delayed diagnosis of vertically acquired HIV infection

Psychosocial adjustment and quality of life in children undergoing screening in a specialist paediatric hypertrophic cardiomyopathy clinic

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

Cardiac phenotype in ATP1A3 -related syndromes: A multicenter cohort study

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