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Haemodynamic definitions and updated clinical classification of pulmonary hypertension

The European respiratory journal, 2019-01, Vol.53 (1), p.1801913

2019

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Adult congenital heart disease: Past, present and future

Acta Paediatrica, 2019-10, Vol.108 (10), p.1757-1764

2019

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Pulmonary arterial hypertension in adult congenital heart disease

Heart (British Cardiac Society), 2018-10, Vol.104 (19), p.1568-1574

2018

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Updated Clinical Classification of Pulmonary Hypertension

Journal of the American College of Cardiology, 2013-12, Vol.62 (25), p.D34-D41

2013

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A propensity score-adjusted analysis of clinical outcomes after pulmonary valve replacement in tetralogy of Fallot

Heart (British Cardiac Society), 2018-05, Vol.104 (9), p.738-744

2018

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Atrial septal defect closure in adulthood is associated with normal survival in the mid to longer term

Heart (British Cardiac Society), 2019-07, Vol.105 (13), p.1014-1019

2019

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Outcome of cardiac surgery in patients with congenital heart disease in England between 1997 and 2015

PloS one, 2017-06, Vol.12 (6), p.e0178963-e0178963

2017

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Clinical Outcomes of Surgical Pulmonary Valve Replacement After Repair of Tetralogy of Fallot and Potential Prognostic Value of Preoperative Cardiopulmonary Exercise Testing

Circulation (New York, N.Y.), 2014-01, Vol.129 (1), p.18-27

2014

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Implantable Cardioverter-Defibrillators in Tetralogy of Fallot

Circulation (New York, N.Y.), 2008-01, Vol.117 (3), p.363-370

2008

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Cardiac magnetic resonance markers of progressive RV dilation and dysfunction after tetralogy of Fallot repair

Heart (British Cardiac Society), 2015-11, Vol.101 (21), p.1724-1730

2015

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Echocardiographic Predictors of Outcome in Eisenmenger Syndrome

Circulation (New York, N.Y.), 2012-09, Vol.126 (12), p.1461-1468

2012

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The ESC Working Group on Adult Congenital Heart Disease

European heart journal, 2020-05, Vol.41 (20), p.1870-1871

2020

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Early mortality and concomitant procedures related to Fontan conversion: Quantitative analysis

International journal of cardiology, 2017-06, Vol.236, p.132-137

2017

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Effect of maternal heart disease on fetal growth

Obstetrics and gynecology (New York. 1953), 2011-04, Vol.117 (4), p.886-891

2011

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Major adverse events and atrial tachycardia in Ebstein’s anomaly predicted by cardiovascular magnetic resonance

Heart (British Cardiac Society), 2018-01, Vol.104 (1), p.37-44

2018

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Survival in portopulmonary hypertension: Outcomes of the united kingdom national pulmonary arterial hypertension registry

The Journal of heart and lung transplantation, 2017-07, Vol.36 (7), p.770-779

2017

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Systemic Right Ventricle in Adults With Congenital Heart Disease: Anatomic and Phenotypic Spectrum and Current Approach to Management

Circulation (New York, N.Y.), 2018-01, Vol.137 (5), p.508-518

2018

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COVID-19 and congenital heart disease in perspective

European heart journal, 2020-05, Vol.41 (20), p.1871-1872

Gatzoulis, Michael A

2020

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Surgical and percutaneous pulmonary valve replacement in England over the past two decades

Heart (British Cardiac Society), 2019-06, Vol.105 (12), p.932-937

2019

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Outcome in adult patients after arterial switch operation for transposition of the great arteries

International journal of cardiology, 2013-09, Vol.167 (6), p.2588-2593

2013

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Perinatal Changes in Fetal Ventricular Geometry, Myocardial Performance, and Cardiac Function in Normal Term Pregnancies

Journal of the American Society of Echocardiography, 2017-05, Vol.30 (5), p.485-492.e5

2017

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Digital technology and artificial intelligence for improving congenital heart disease care: alea iacta est

European heart journal, 2024-04, Vol.45 (16), p.1386-1389

2024

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Definition and Management of Segmental Pulmonary Hypertension

Journal of the American Heart Association, 2018-07, Vol.7 (14)

2018

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Longer-term bosentan therapy improves functional capacity in Eisenmenger syndrome: Results of the BREATHE-5 open-label extension study

International journal of cardiology, 2008-06, Vol.127 (1), p.27-32

2008

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Haemodynamic definitions and updated clinical classification of pulmonary hypertension

Adult congenital heart disease: Past, present and future

Pulmonary arterial hypertension in adult congenital heart disease

Updated Clinical Classification of Pulmonary Hypertension

2019 updated consensus statement on the diagnosis and treatment of pediatric pulmonary hypertension: The European Pediatric Pulmonary Vascular Disease Network (EPPVDN), endorsed by AEPC, ESPR and ISHLT

A propensity score-adjusted analysis of clinical outcomes after pulmonary valve replacement in tetralogy of Fallot

Atrial septal defect closure in adulthood is associated with normal survival in the mid to longer term

Outcome of cardiac surgery in patients with congenital heart disease in England between 1997 and 2015

Clinical Outcomes of Surgical Pulmonary Valve Replacement After Repair of Tetralogy of Fallot and Potential Prognostic Value of Preoperative Cardiopulmonary Exercise Testing

Implantable Cardioverter-Defibrillators in Tetralogy of Fallot

Cardiac magnetic resonance markers of progressive RV dilation and dysfunction after tetralogy of Fallot repair

Echocardiographic Predictors of Outcome in Eisenmenger Syndrome

The ESC Working Group on Adult Congenital Heart Disease

Early mortality and concomitant procedures related to Fontan conversion: Quantitative analysis

Effect of maternal heart disease on fetal growth

Major adverse events and atrial tachycardia in Ebstein’s anomaly predicted by cardiovascular magnetic resonance

Survival in portopulmonary hypertension: Outcomes of the united kingdom national pulmonary arterial hypertension registry

Systemic Right Ventricle in Adults With Congenital Heart Disease: Anatomic and Phenotypic Spectrum and Current Approach to Management

COVID-19 and congenital heart disease in perspective

Surgical and percutaneous pulmonary valve replacement in England over the past two decades

Outcome in adult patients after arterial switch operation for transposition of the great arteries

Perinatal Changes in Fetal Ventricular Geometry, Myocardial Performance, and Cardiac Function in Normal Term Pregnancies

Digital technology and artificial intelligence for improving congenital heart disease care: alea iacta est

Definition and Management of Segmental Pulmonary Hypertension

Longer-term bosentan therapy improves functional capacity in Eisenmenger syndrome: Results of the BREATHE-5 open-label extension study

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