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Marfan Sartan: a randomized, double-blind, placebo-controlled trial

European heart journal, 2015-08, Vol.36 (32), p.2160-2166

2015

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MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

American journal of human genetics, 2014-12, Vol.95 (6), p.736-743

2014

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Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study

Orphanet journal of rare diseases, 2024-04, Vol.19 (1), p.180-180

2024

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The usefulness of 3D printed heart models for medical student education in congenital heart disease

BMC medical education, 2021-09, Vol.21 (1), p.1-480, Article 480

2021

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TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Nature communications, 2024-04, Vol.15 (1), p.3380-3380

2024

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Parental mosaicism in Marfan and Ehlers-Danlos syndromes and related disorders

European journal of human genetics : EJHG, 2021-05, Vol.29 (5), p.771-779

2021

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Impact of a transition education program on health-related quality of life in pediatric patients with congenital heart disease: study design for a randomised controlled trial

Health and quality of life outcomes, 2021-01, Vol.19 (1), p.23-23, Article 23

2021

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Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methods

Health and quality of life outcomes, 2021-07, Vol.19 (1), p.1-187, Article 187

2021

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FUTURE-2: Results from an open-label, long-term safety and tolerability extension study using the pediatric FormUlation of bosenTan in pUlmonary arterial hypeRtEnsion

International journal of cardiology, 2016-01, Vol.202, p.52-58

2016

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Advancing paediatric cardiac imaging: a comprehensive analysis of the feasibility and accuracy of a novel 3D paediatric transoesophageal probe

Frontiers in cardiovascular medicine, 2023-12, Vol.10, p.1294109-1294109

2023

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Assessment of Ventricular Septal Defect Size and Morphology by Three-Dimensional Transthoracic Echocardiography

Journal of the American Society of Echocardiography, 2016-08, Vol.29 (8), p.777-785

2016

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Outcome of coronary artery bypass grafting performed in young children

The Journal of thoracic and cardiovascular surgery, 2010-02, Vol.139 (2), p.349-353

2010

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Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of Age

Journal of clinical medicine, 2023-04, Vol.12 (8), p.2902

2023

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Impact of 3D-printed models in meetings with parents of children undergoing interventional cardiac catheterisation

Frontiers in pediatrics, 2023-01, Vol.10, p.947340-947340

2023

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Effect of Beta-Blockade on Ascending Aortic Dilatation in Children With the Marfan Syndrome

The American journal of cardiology, 2007-02, Vol.99 (3), p.406-409

2007

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A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus

Molecular genetics & genomic medicine, 2021-11, Vol.9 (11), p.e1814-n/a

2021

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Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature

Molecular genetics & genomic medicine, 2020-05, Vol.8 (5), p.e1132-n/a

2020

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Corrigendum to “FUTURE-2: Results from an open-label, long-term safety and tolerability extension study using the pediatric FormUlation of bosenTan in pUlmonary arterial hypeRtEnsion” [Int. J. Cardiol. 202 (2016) 52–58]

International journal of cardiology, 2016-11, Vol.223, p.1072-1073

2016

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Cardiac strangulation: An atypical complication from epicardial pacemaker leads in a newborn

Annals of pediatric cardiology, 2018-05, Vol.11 (2), p.191-193

2018

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Impact of Sophrology on cardiopulmonary fitness in teenagers and young adults with a congenital heart disease: The SOPHROCARE study rationale, design and methods

International journal of cardiology. Heart & vasculature, 2020-04, Vol.27, p.100489-100489, Article 100489

2020

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Echocardiographic Parameters Predictive of Poor Outcome in Persistent Pulmonary Hypertension of the Newborn (PPHN): Preliminary Results

Pediatric cardiology, 2021-12, Vol.42 (8), p.1848-1853

2021

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Three-dimensional printing of a complex CHD to plan surgical repair

Cardiology in the young, 2016-10, Vol.26 (7), p.1432-1434

2016

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Ventricular Septal Defect Area by Three-Dimensional Echocardiography for Assessment of Shunt Severity in Children

Journal of the American Society of Echocardiography, 2021-10, Vol.34 (10), p.1109-1111

2021

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Marfan Sartan: a randomized, double-blind, placebo-controlled trial

MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study

The usefulness of 3D printed heart models for medical student education in congenital heart disease

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Parental mosaicism in Marfan and Ehlers-Danlos syndromes and related disorders

Impact of a transition education program on health-related quality of life in pediatric patients with congenital heart disease: study design for a randomised controlled trial

Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methods

FUTURE-2: Results from an open-label, long-term safety and tolerability extension study using the pediatric FormUlation of bosenTan in pUlmonary arterial hypeRtEnsion

Advancing paediatric cardiac imaging: a comprehensive analysis of the feasibility and accuracy of a novel 3D paediatric transoesophageal probe

Assessment of Ventricular Septal Defect Size and Morphology by Three-Dimensional Transthoracic Echocardiography

Outcome of coronary artery bypass grafting performed in young children

Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of Age

Impact of 3D-printed models in meetings with parents of children undergoing interventional cardiac catheterisation

Effect of Beta-Blockade on Ascending Aortic Dilatation in Children With the Marfan Syndrome

A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus

Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature

Corrigendum to “FUTURE-2: Results from an open-label, long-term safety and tolerability extension study using the pediatric FormUlation of bosenTan in pUlmonary arterial hypeRtEnsion” [Int. J. Cardiol. 202 (2016) 52–58]

Parental Electrocardiographic Screening Identifies a High Degree of Inheritance for Congenital and Childhood Nonimmune Isolated Atrioventricular Block

Cardiac strangulation: An atypical complication from epicardial pacemaker leads in a newborn

Impact of Sophrology on cardiopulmonary fitness in teenagers and young adults with a congenital heart disease: The SOPHROCARE study rationale, design and methods

The Impact of Clinical and Genetic Findings on The Management of Young Brugada Syndrome Patients

Echocardiographic Parameters Predictive of Poor Outcome in Persistent Pulmonary Hypertension of the Newborn (PPHN): Preliminary Results

Three-dimensional printing of a complex CHD to plan surgical repair

Ventricular Septal Defect Area by Three-Dimensional Echocardiography for Assessment of Shunt Severity in Children

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