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Prolonged overcirculation-induced pulmonary arterial hypertension as a cause of right ventricular failure

European heart journal, 2012-04, Vol.33 (8), p.1017-1026

2012

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Pulmonary arterial hypertension associated with congenital heart disease: Recent advances and future directions

International journal of cardiology, 2014-12, Vol.177 (2), p.340-347

2014

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Role of Cardiac Magnetic Resonance Imaging in the Management of Patients With Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2008-11, Vol.52 (21), p.1683-1692

2008

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Early echocardiographic evaluation of right ventricular load adaptability after sequential combination treatment in pulmonary arterial hypertension

Herz, 2023-08, Vol.48 (4), p.316-324

2023

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Clinical and Prognostic Relevance of Echocardiographic Evaluation of Right Ventricular Geometry in Patients With Idiopathic Pulmonary Arterial Hypertension

The American journal of cardiology, 2011-02, Vol.107 (4), p.628-632

2011

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Impact of pulmonary hypertension on outcomes after aortic valve replacement for aortic valve stenosis

The Journal of thoracic and cardiovascular surgery, 2011-06, Vol.141 (6), p.1424-1430

2011

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PET Imaging May Provide a Novel Biomarker and Understanding of Right Ventricular Dysfunction in Patients With Idiopathic Pulmonary Arterial Hypertension

Circulation. Cardiovascular imaging, 2011-11, Vol.4 (6), p.641-647

2011

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Prolonged beneficial effect of bosentan treatment and 4-year survival rates in adult patients with pulmonary arterial hypertension associated with congenital heart disease

International journal of cardiology, 2013-03, Vol.164 (1), p.64-69

2013

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Pulmonary arterial hypertension in adults born with a heart septal defect: the Euro Heart Survey on adult congenital heart disease

Heart (British Cardiac Society), 2007-06, Vol.93 (6), p.682-687

2007

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Serum soluble ST2 and interleukin-33 levels in patients with pulmonary arterial hypertension

International journal of cardiology, 2013-09, Vol.168 (2), p.1545-1547

2013

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Therapy for pulmonary arterial hypertension due to congenital heart disease and Down's syndrome

International journal of cardiology, 2013-04, Vol.164 (3), p.323-326

2013

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Right atrial volume and phasic function in pulmonary hypertension

International journal of cardiology, 2013-09, Vol.168 (1), p.420-426

2013

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Significance of Echocardiographic Assessment for Right Ventricular Function After Balloon Pulmonary Angioplasty in Patients With Chronic Thromboembolic Induced Pulmonary Hypertension

The American journal of cardiology, 2015-01, Vol.115 (2), p.256-261

2015

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Prognostic implications of pulmonary hypertension in patients with severe aortic stenosis

The Journal of thoracic and cardiovascular surgery, 2011-10, Vol.142 (4), p.800-808

2011

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Long-term results from the EARLY study of bosentan in WHO functional class II pulmonary arterial hypertension patients

International journal of cardiology, 2014-03, Vol.172 (2), p.332-339

2014

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Treatment of segmental pulmonary artery hypertension in adults with congenital heart disease

International journal of cardiology, 2013-03, Vol.164 (1), p.106-110

2013

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Left Ventricular Diastolic Dysfunction Predicts Mortality in Patients With Systemic Sclerosis

Journal of the American College of Cardiology, 2018-10, Vol.72 (15), p.1804-1813

2018

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A Simple Echocardiographic Prediction Rule for Hemodynamics in Pulmonary Hypertension

Circulation. Cardiovascular imaging, 2012-11, Vol.5 (6), p.765-775

2012

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Venovenous extracorporeal membrane oxygenation using a single cannula in patients with pulmonary hypertension and atrial septal defects

The Journal of thoracic and cardiovascular surgery, 2012-04, Vol.143 (4), p.982-984

2012

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Ambrisentan for Pulmonary Arterial Hypertension Due to Congenital Heart Disease

The American journal of cardiology, 2011-05, Vol.107 (9), p.1381-1385

2011

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C-reactive protein in adults with pulmonary arterial hypertension associated with congenital heart disease and its prognostic value

Heart (British Cardiac Society), 2014-09, Vol.100 (17), p.1335-1341

2014

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Quercetin regulates pulmonary vascular remodeling in pulmonary hypertension by downregulating TGF-β1-Smad2/3 pathway

BMC cardiovascular disorders, 2024-10, Vol.24 (1), p.535-16, Article 535

2024

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Pulmonary arterial capacitance in children with idiopathic pulmonary arterial hypertension and pulmonary arterial hypertension associated with congenital heart disease: Relation to pulmonary vascular resistance, exercise capacity, and survival

The American heart journal, 2011-09, Vol.162 (3), p.562-568

2011

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Abnormal left ventricular diastolic filling in chronic thromboembolic pulmonary hypertension : True diastolic dysfunction or left ventricular underfilling?

Journal of the American College of Cardiology, 2007-03, Vol.49 (12), p.1334-1339

2007

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Prolonged overcirculation-induced pulmonary arterial hypertension as a cause of right ventricular failure

Pulmonary arterial hypertension associated with congenital heart disease: Recent advances and future directions

Role of Cardiac Magnetic Resonance Imaging in the Management of Patients With Pulmonary Arterial Hypertension

Early echocardiographic evaluation of right ventricular load adaptability after sequential combination treatment in pulmonary arterial hypertension

Clinical and Prognostic Relevance of Echocardiographic Evaluation of Right Ventricular Geometry in Patients With Idiopathic Pulmonary Arterial Hypertension

Impact of pulmonary hypertension on outcomes after aortic valve replacement for aortic valve stenosis

Clinical Profile, Prognostic Implication, and Response to Treatment of Pulmonary Hypertension in Patients With Severe Aortic Stenosis

PET Imaging May Provide a Novel Biomarker and Understanding of Right Ventricular Dysfunction in Patients With Idiopathic Pulmonary Arterial Hypertension

Prolonged beneficial effect of bosentan treatment and 4-year survival rates in adult patients with pulmonary arterial hypertension associated with congenital heart disease

Pulmonary arterial hypertension in adults born with a heart septal defect: the Euro Heart Survey on adult congenital heart disease

Serum soluble ST2 and interleukin-33 levels in patients with pulmonary arterial hypertension

Therapy for pulmonary arterial hypertension due to congenital heart disease and Down's syndrome

Right atrial volume and phasic function in pulmonary hypertension

Significance of Echocardiographic Assessment for Right Ventricular Function After Balloon Pulmonary Angioplasty in Patients With Chronic Thromboembolic Induced Pulmonary Hypertension

Prognostic implications of pulmonary hypertension in patients with severe aortic stenosis

Long-term results from the EARLY study of bosentan in WHO functional class II pulmonary arterial hypertension patients

Treatment of segmental pulmonary artery hypertension in adults with congenital heart disease

Left Ventricular Diastolic Dysfunction Predicts Mortality in Patients With Systemic Sclerosis

A Simple Echocardiographic Prediction Rule for Hemodynamics in Pulmonary Hypertension

Venovenous extracorporeal membrane oxygenation using a single cannula in patients with pulmonary hypertension and atrial septal defects

Ambrisentan for Pulmonary Arterial Hypertension Due to Congenital Heart Disease

C-reactive protein in adults with pulmonary arterial hypertension associated with congenital heart disease and its prognostic value

Quercetin regulates pulmonary vascular remodeling in pulmonary hypertension by downregulating TGF-β1-Smad2/3 pathway

Pulmonary arterial capacitance in children with idiopathic pulmonary arterial hypertension and pulmonary arterial hypertension associated with congenital heart disease: Relation to pulmonary vascular resistance, exercise capacity, and survival

Abnormal left ventricular diastolic filling in chronic thromboembolic pulmonary hypertension : True diastolic dysfunction or left ventricular underfilling?

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