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An Evaluation of Long-term Survival From Time of Diagnosis in Pulmonary Arterial Hypertension From the REVEAL Registry

Chest, 2012-08, Vol.142 (2), p.448-456

2012

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Five-Year Outcomes of Patients Enrolled in the REVEAL Registry

Chest, 2015-10, Vol.148 (4), p.1043-1054

2015

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Updated Treatment Algorithm of Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2013-12, Vol.62 (25), p.D60-D72

2013

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The importance of patient perspectives in pulmonary hypertension

The European respiratory journal, 2019-01, Vol.53 (1), p.1801919

2019

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Predicting outcomes in pulmonary arterial hypertension based on the 6-minute walk distance

The Journal of heart and lung transplantation, 2015-03, Vol.34 (3), p.362-368

2015

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The REVEAL Registry Risk Score Calculator in Patients Newly Diagnosed With Pulmonary Arterial Hypertension

Chest, 2012-02, Vol.141 (2), p.354-362

2012

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The 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: a practical chronicle of progress

The European respiratory journal, 2015-10, Vol.46 (4), p.879-882

2015

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Role of Serial Quantitative Assessment of Right Ventricular Function by Strain in Pulmonary Arterial Hypertension

The American journal of cardiology, 2013, Vol.111 (1), p.143-148

2013

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Long-Term Ambrisentan Therapy for the Treatment of Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2009-11, Vol.54 (21), p.1971-1981

2009

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Right Ventricular Strain for Prediction of Survival in Patients With Pulmonary Arterial Hypertension

Chest, 2011-06, Vol.139 (6), p.1299-1309

2011

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Four- and Seven-Year Outcomes of Patients With Congenital Heart Disease–Associated Pulmonary Arterial Hypertension (from the REVEAL Registry)

The American journal of cardiology, 2014, Vol.113 (1), p.147-155

2014

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Sex Differences in the Diagnosis, Treatment, and Outcome of Patients With Pulmonary Arterial Hypertension Enrolled in the Registry to Evaluate Early and Long-term Pulmonary Arterial Hypertension Disease Management

Chest, 2012-02, Vol.141 (2), p.363-373

2012

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Prognostic implications of serial risk score assessments in patients with pulmonary arterial hypertension: A Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL) analysis

The Journal of heart and lung transplantation, 2015-03, Vol.34 (3), p.356-361

2015

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Functional Class Improvement and 3-Year Survival Outcomes in Patients With Pulmonary Arterial Hypertension in the REVEAL Registry

Chest, 2013-07, Vol.144 (1), p.160-168

2013

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Relationship of Pulmonary Arterial Capacitance and Mortality in Idiopathic Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2006-02, Vol.47 (4), p.799-803

2006

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Pulmonary Hypertension in Hereditary Hemorrhagic Telangiectasia

Chest, 2016-02, Vol.149 (2), p.362-371

2016

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Portopulmonary hypertension: Results from a 10‐year screening algorithm

Hepatology (Baltimore, Md.), 2006-12, Vol.44 (6), p.1502-1510

2006

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Characterization of First-Time Hospitalizations in Patients With Newly Diagnosed Pulmonary Arterial Hypertension in the REVEAL Registry

Chest, 2014-11, Vol.146 (5), p.1263-1273

2014

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Validation of two predictive models for survival in pulmonary arterial hypertension

The European respiratory journal, 2015-07, Vol.46 (1), p.152-164

2015

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Treatment of patients with pulmonary arterial hypertension at the time of death or deterioration to functional class IV: Insights from the REVEAL Registry

The Journal of heart and lung transplantation, 2013-11, Vol.32 (11), p.1114-1122

2013

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Integration of Clinical and Hemodynamic Parameters in the Prediction of Long-term Survival in Patients With Pulmonary Arterial Hypertension

Chest, 2011-06, Vol.139 (6), p.1285-1293

2011

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Pulmonary Hypertension: Diagnosis and Management

Mayo Clinic proceedings, 2009-02, Vol.84 (2), p.191-207

2009

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Impact of declining renal function on outcomes in pulmonary arterial hypertension: A REVEAL registry analysis

The Journal of heart and lung transplantation, 2018-06, Vol.37 (6), p.696-705

2018

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Ambrisentan Therapy in Patients With Pulmonary Arterial Hypertension Who Discontinued Bosentan or Sitaxsentan Due to Liver Function Test Abnormalities

Chest, 2009-01, Vol.135 (1), p.122-129

2009

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Predicting Survival in Patients With Pulmonary Arterial Hypertension: The REVEAL Risk Score Calculator 2.0 and Comparison With ESC/ERS-Based Risk Assessment Strategies

Chest, 2019-08, Vol.156 (2), p.323-337

2019

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An Evaluation of Long-term Survival From Time of Diagnosis in Pulmonary Arterial Hypertension From the REVEAL Registry

Five-Year Outcomes of Patients Enrolled in the REVEAL Registry

Updated Treatment Algorithm of Pulmonary Arterial Hypertension

The importance of patient perspectives in pulmonary hypertension

Predicting outcomes in pulmonary arterial hypertension based on the 6-minute walk distance

The REVEAL Registry Risk Score Calculator in Patients Newly Diagnosed With Pulmonary Arterial Hypertension

The 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: a practical chronicle of progress

Role of Serial Quantitative Assessment of Right Ventricular Function by Strain in Pulmonary Arterial Hypertension

Long-Term Ambrisentan Therapy for the Treatment of Pulmonary Arterial Hypertension

Right Ventricular Strain for Prediction of Survival in Patients With Pulmonary Arterial Hypertension

Four- and Seven-Year Outcomes of Patients With Congenital Heart Disease–Associated Pulmonary Arterial Hypertension (from the REVEAL Registry)

Sex Differences in the Diagnosis, Treatment, and Outcome of Patients With Pulmonary Arterial Hypertension Enrolled in the Registry to Evaluate Early and Long-term Pulmonary Arterial Hypertension Disease Management

Prognostic implications of serial risk score assessments in patients with pulmonary arterial hypertension: A Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL) analysis

Functional Class Improvement and 3-Year Survival Outcomes in Patients With Pulmonary Arterial Hypertension in the REVEAL Registry

Relationship of Pulmonary Arterial Capacitance and Mortality in Idiopathic Pulmonary Arterial Hypertension

Pulmonary Hypertension in Hereditary Hemorrhagic Telangiectasia

Portopulmonary hypertension: Results from a 10‐year screening algorithm

Characterization of First-Time Hospitalizations in Patients With Newly Diagnosed Pulmonary Arterial Hypertension in the REVEAL Registry

Validation of two predictive models for survival in pulmonary arterial hypertension

Treatment of patients with pulmonary arterial hypertension at the time of death or deterioration to functional class IV: Insights from the REVEAL Registry

Integration of Clinical and Hemodynamic Parameters in the Prediction of Long-term Survival in Patients With Pulmonary Arterial Hypertension

Pulmonary Hypertension: Diagnosis and Management

Impact of declining renal function on outcomes in pulmonary arterial hypertension: A REVEAL registry analysis

Ambrisentan Therapy in Patients With Pulmonary Arterial Hypertension Who Discontinued Bosentan or Sitaxsentan Due to Liver Function Test Abnormalities

Predicting Survival in Patients With Pulmonary Arterial Hypertension: The REVEAL Risk Score Calculator 2.0 and Comparison With ESC/ERS-Based Risk Assessment Strategies

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