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2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension

The European respiratory journal, 2015-10, Vol.46 (4), p.903-975

2015

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Acute Heart Failure in Multisystem Inflammatory Syndrome in Children in the Context of Global SARS-CoV-2 Pandemic

Circulation (New York, N.Y.), 2020-08, Vol.142 (5), p.429-436

2020

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Echocardiographic Evaluation of Pulmonary Pressures and Right Ventricular Function after Pediatric Cardiac Surgery: A Simple Approach for the Intensivist

Frontiers in pediatrics, 2017-08, Vol.5, p.184-184

Beghetti, Maurice

2017

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Physical Activity Reduces Systemic Blood Pressure and Improves Early Markers of Atherosclerosis in Pre-Pubertal Obese Children

Journal of the American College of Cardiology, 2009-12, Vol.54 (25), p.2396-2406

2009

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Bosentan in pediatric patients with pulmonary arterial hypertension

Current vascular pharmacology, 2009-04, Vol.7 (2), p.225-233

Beghetti, Maurice

2009

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Pediatric Pulmonary Hypertension

Journal of the American College of Cardiology, 2013-12, Vol.62 (25), p.D117-D126

2013

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Clinical features of paediatric pulmonary hypertension: a registry study

The Lancet (British edition), 2012-02, Vol.379 (9815), p.537-546

2012

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Updated Clinical Classification of Pulmonary Hypertension

Journal of the American College of Cardiology, 2009-06, Vol.54 (1), p.S43-S54

2009

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Assessment of Operability of Patients With Pulmonary Arterial Hypertension Associated With Congenital Heart Disease: Do We Have the Good Tools to Predict Success?

Circulation Journal, 2014, Vol.78(1), pp.4-11

2014

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Bosentan as Adjunctive Therapy for Persistent Pulmonary Hypertension of the Newborn: Results of the Randomized Multicenter Placebo-Controlled Exploratory Trial

The Journal of pediatrics, 2016-10, Vol.177, p.90-96.e3

2016

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Clinical classification of pulmonary hypertension

Journal of the American College of Cardiology, 2004-06, Vol.43 (12), p.S5-S12

2004

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Efficacy and safety of oral sildenafil in children with Down syndrome and pulmonary hypertension

BMC cardiovascular disorders, 2017-07, Vol.17 (1), p.177-177, Article 177

2017

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Endothelial glycocalyx degradation in multisystem inflammatory syndrome in children related to COVID-19

Journal of molecular medicine (Berlin, Germany), 2022-05, Vol.100 (5), p.735-746

2022

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Growing up with Idiopathic Pulmonary Arterial Hypertension: An Arduous Journey

Pediatric reports, 2023-05, Vol.15 (2), p.301-310

2023

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An update on current and emerging treatments for pulmonary arterial hypertension in childhood and adolescence

Expert review of respiratory medicine, 2019-02, Vol.13 (2), p.205-215

2019

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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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Medical Therapy for Pediatric Pulmonary Arterial Hypertension

The Journal of pediatrics, 2010-10, Vol.157 (4), p.528-532

2010

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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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Use of CO2-Derived Variables in Cardiac Intensive Care Unit: Pathophysiology and Clinical Implications

Journal of cardiovascular development and disease, 2023-05, Vol.10 (5), p.208

2023

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Fulminant Infective Endocarditis Due to Kingella Kingae and Several Complications in a 6-Year-Old Girl: A Case Report

Frontiers in pediatrics, 2021-07, Vol.9

2021

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Home Respiratory Polygraphy and Spirometry in Normal Weight and Children with Obesity Suspected for Obstructive Sleep Apnea Syndrome: Are There Any Associations?

Pulmonary medicine, 2023-01, Vol.2023, p.1532443-7

2023

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Short- and Long-Term Effects of Inhaled Iloprost Therapy in Children With Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2008-01, Vol.51 (2), p.161-169

2008

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International registry of congenital porto-systemic shunts: a multi-centre, retrospective and prospective registry of neonates, children and adults with congenital porto-systemic shunts

Orphanet journal of rare diseases, 2022-07, Vol.17 (1), p.1-284, Article 284

2022

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Application of a modified clinical classification for pulmonary arterial hypertension associated with congenital heart disease in children: emphasis on atrial septal defects and transposition of the great arteries. An analysis from the TOPP registry

Frontiers in cardiovascular medicine, 2024, Vol.11, p.1344014-1344014

2024

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The challenges in paediatric pulmonary arterial hypertension

European respiratory review, 2014-12, Vol.23 (134), p.498-504

2014

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2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension

Acute Heart Failure in Multisystem Inflammatory Syndrome in Children in the Context of Global SARS-CoV-2 Pandemic

Echocardiographic Evaluation of Pulmonary Pressures and Right Ventricular Function after Pediatric Cardiac Surgery: A Simple Approach for the Intensivist

Physical Activity Reduces Systemic Blood Pressure and Improves Early Markers of Atherosclerosis in Pre-Pubertal Obese Children

Bosentan in pediatric patients with pulmonary arterial hypertension

Pediatric Pulmonary Hypertension

Clinical features of paediatric pulmonary hypertension: a registry study

Updated Clinical Classification of Pulmonary Hypertension

Assessment of Operability of Patients With Pulmonary Arterial Hypertension Associated With Congenital Heart Disease: Do We Have the Good Tools to Predict Success?

Bosentan as Adjunctive Therapy for Persistent Pulmonary Hypertension of the Newborn: Results of the Randomized Multicenter Placebo-Controlled Exploratory Trial

Clinical classification of pulmonary hypertension

Efficacy and safety of oral sildenafil in children with Down syndrome and pulmonary hypertension

Endothelial glycocalyx degradation in multisystem inflammatory syndrome in children related to COVID-19

Growing up with Idiopathic Pulmonary Arterial Hypertension: An Arduous Journey

An update on current and emerging treatments for pulmonary arterial hypertension in childhood and adolescence

Definition and Management of Segmental Pulmonary Hypertension

Medical Therapy for Pediatric Pulmonary Arterial Hypertension

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

Use of CO2-Derived Variables in Cardiac Intensive Care Unit: Pathophysiology and Clinical Implications

Fulminant Infective Endocarditis Due to Kingella Kingae and Several Complications in a 6-Year-Old Girl: A Case Report

Home Respiratory Polygraphy and Spirometry in Normal Weight and Children with Obesity Suspected for Obstructive Sleep Apnea Syndrome: Are There Any Associations?

Short- and Long-Term Effects of Inhaled Iloprost Therapy in Children With Pulmonary Arterial Hypertension

International registry of congenital porto-systemic shunts: a multi-centre, retrospective and prospective registry of neonates, children and adults with congenital porto-systemic shunts

Application of a modified clinical classification for pulmonary arterial hypertension associated with congenital heart disease in children: emphasis on atrial septal defects and transposition of the great arteries. An analysis from the TOPP registry

The challenges in paediatric pulmonary arterial hypertension

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