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Is cardiac resynchronization therapy for right ventricular failure in pulmonary arterial hypertension of benefit?World Health Organization Group I Pulmonary Hypertension: Epidemiology and Pathophysiology.The Critical Role of Pulmonary Arterial Compliance in Pulmonary Hypertension.Late-onset pulmonary arterial hypertension in repaired D-transposition of great arteries: an uncommon complicationLung ¹⁸F-fluorodeoxyglucose positron emission tomography for diagnosis and monitoring of pulmonary arterial hypertensionValidation of high-resolution echocardiography and magnetic resonance imaging vs. high-fidelity catheterization in experimental pulmonary hypertension.The WHO classification of pulmonary hypertension: A case-based imaging compendium.QTc prolongation is associated with impaired right ventricular function and predicts mortality in pulmonary hypertension.United States validation of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR).A systematic review and meta-analysis of trials using statins in pulmonary arterial hypertension.Pulmonary pulse wave transit time is associated with right ventricular-pulmonary artery coupling in pulmonary arterial hypertension.Epidemiology of pulmonary hypertension and right ventricular failure in left heart failure.Pulmonary hypertension secondary to heart failure with preserved ejection fraction.Chronic use of PAH-specific therapy in World Health Organization Group III Pulmonary Hypertension: a systematic review and meta-analysisEvolving Concepts of Pulmonary Hypertension Secondary to Left Heart Disease.Update in treatment options in pulmonary hypertension.CD28/B7 Deficiency Attenuates Systolic Overload-Induced Congestive Heart Failure, Myocardial and Pulmonary Inflammation, and Activated T Cell Accumulation in the Heart and Lungs.Resistance over compliance describes right ventricular afterload better than resistance-compliance time: a friendly amendment.Usefulness of red cell distribution width as a prognostic marker in pulmonary hypertension.Association of serum creatinine with abnormal hemodynamics and mortality in pulmonary arterial hypertension.Colchicine Depolymerizes Microtubules, Increases Junctophilin-2, and Improves Right Ventricular Function in Experimental Pulmonary Arterial Hypertension.Adding fuel to the fire: Coronary artery dissection complicating blunt chest trauma.Air in the Left Ventricle. An Unusual Case of Endocarditis.Interleukin-6 is independently associated with right ventricular function in pulmonary arterial hypertension.The heterogeneity of heart failure: will enhanced phenotyping be necessary for future clinical trial success?Disproportionate Right Ventricular Dysfunction and Poor Survival in Group 3 Pulmonary Hypertension.The Nitric Oxide Pathway-A Potential Target for Precision Medicine in Pulmonary Arterial Hypertension.Pulmonary hypertension in chronic kidney disease: a hemodynamic characterization.Treatment of left ventricular assist device thrombosis with extended catheter-directed intraventricular thrombolytic therapy.Trends and Outcomes of Pulmonary Arterial Hypertension-Related Hospitalizations in the United States: Analysis of the Nationwide Inpatient Sample Database From 2001 Through 2012.Clinical characteristics of pulmonary hypertension in patients with heart failure and preserved ejection fraction.Validation of the pulmonary hypertension connection equation for survival prediction in pulmonary arterial hypertension.The End Is Near... Do We Know Everything About Cardiopulmonary Exercise Testing in HF Patients?Out with the old, in with the new: an updated risk stratification equation for pulmonary arterial hypertension.A USA-based registry for pulmonary arterial hypertension: 1982-2006.Survival in pulmonary arterial hypertension: a reappraisal of the NIH risk stratification equation.Pulmonary arterial hypertension: pathogenesis and clinical management.Reply: applying cluster analysis to data of previously published chronic heart failure trials.Telangiectasia and Pulmonary Arterial Hypertension Following Treatment With Trastuzumab Emtansine: A Case Report.Isolated heart transplantation for familial transthyretin (TTR) V122I cardiac amyloidosis
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