All Stories

  1. Subendocardial Involvement as an Underrecognized Cardiac MRI Phenotype in Myocarditis
  2. Effect of riociguat on right ventricular function in patients with pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension
  3. Clinical features and survival in Takayasu’s arteritis-associated pulmonary hypertension: a nationwide study
  4. Identification of Hypoxia Induced Metabolism Associated Genes in Pulmonary Hypertension
  5. Radiofrequency Catheter Ablation of Supraventricular Tachycardia in Patients With Pulmonary Hypertension: Feasibility and Long-Term Outcome
  6. Association Between Anticoagulation Outcomes and Venous Thromboembolism History in Chronic Thromboembolic Pulmonary Hypertension
  7. Venous thromboembolism in Asia and worldwide: Emerging insights from GARFIELD-VTE
  8. A Personalized Pulmonary Circulation Model to Non-Invasively Calculate Fractional Flow Reserve for Artery Stenosis Detection
  9. DNA methyltransferase 3B deficiency unveils a new pathological mechanism of pulmonary hypertension
  10. Association between congenital thrombophilia and outcomes in pulmonary embolism patients
  11. Generation of an induced pluripotent stem cell line (PUMCHi006-A) derived from a patient with pulmonary arterial hypertension carrying heterozygous c.1339 G > A mutation in PTGIS gene
  12. Inflammation and cardiovascular diseases
  13. Alteration of Extracellular Superoxide Dismutase in Idiopathic Pulmonary Arterial Hypertension
  14. The features of rare pathogenic BMPR2 variants in pulmonary arterial hypertension: Comparison between patients and reference population
  15. How should a physician approach the pharmacological management of chronic thromboembolic pulmonary hypertension?
  16. Effect of ambrisentan on echocardiographic and Doppler measures from patients in China with pulmonary arterial hypertension
  17. Efficacy and safety of ambrisentan in Chinese patients with connective tissue disease-pulmonary arterial hypertension: a post-hoc analysis
  18. Derivation of an induced pluripotent stem cell line (PUMCHi003-A) from a patient with pulmonary arterial hypertension carrying heterozygous mutation in PTGIS gene
  19. Cancer associated thrombosis in everyday practice: perspectives from GARFIELD-VTE
  20. Spermine promotes pulmonary vascular remodelling and its synthase is a therapeutic target for pulmonary arterial hypertension
  21. Association of Rare PTGIS Variants With Susceptibility and Pulmonary Vascular Response in Patients With Idiopathic Pulmonary Arterial Hypertension
  22. Protective effects of isorhamnetin on pulmonary arterial hypertension: in vivo and in vitro studies
  23. New Insights into the Use of Direct Oral Anticoagulants in Non-high Risk Thrombotic APS Patients: Literature Review and Subgroup Analysis from a Meta-analysis
  24. CSC Expert Consensus on Principles of Clinical Management of Patients With Severe Emergent Cardiovascular Diseases During the COVID-19 Epidemic
  25. Editorial: Drug Development and Target Discovery in Pulmonary Vascular Diseases
  26. Challenges and Special Aspects of Pulmonary Hypertension in Middle- to Low-Income Regions
  27. Micro RNA ‐483 amelioration of experimental pulmonary hypertension
  28. Recommendations from the Peking Union Medical College Hospital for the management of acute myocardial infarction during the COVID-19 outbreak
  29. The Key Laboratory of Pulmonary Vascular Medicine, Chinese Academy of Medical Sciences (KLPVM-CAMS)
  30. Protective effects of 18β-glycyrrhetinic acid on pulmonary arterial hypertension via regulation of Rho A/Rho kinsase pathway
  31. Association Between High FSH, Low Progesterone, and Idiopathic Pulmonary Arterial Hypertension in Women of Reproductive Age
  32. Lipocalin-2 Predicts Long-Term Outcome of Normotensive Patients with Acute Pulmonary Embolism
  33. Circulating Plasma Metabolomic Profiles Differentiate Rodent Models of Pulmonary Hypertension and Idiopathic Pulmonary Arterial Hypertension Patients
  34. Antiphospholipid Syndrome in Chronic Thromboembolic Pulmonary Hypertension: A Well-Defined Subgroup of Patients
  35. Adventitial Cell Atlas of wt (Wild Type) and ApoE (Apolipoprotein E)-Deficient Mice Defined by Single-Cell RNA Sequencing
  36. Monocrotaline pyrrole induces pulmonary endothelial damage through binding to and release from erythrocytes in lung during venous blood reoxygenation
  37. Transthoracic Pulmonary Artery Denervation for Pulmonary Arterial Hypertension
  38. Spermine on Endothelial Extracellular Vesicles Mediates Smoking-Induced Pulmonary Hypertension Partially Through Calcium-Sensing Receptor
  39. Characteristics of cardiopulmonary exercise testing of patients with borderline mean pulmonary artery pressure
  40. Management and 1‐Year Outcomes of Patients With Newly Diagnosed Atrial Fibrillation and Chronic Kidney Disease: Results From the Prospective GARFIELD‐AF Registry
  41. Prevalence of antiphospholipid (aPL) antibodies among patients with chronic thromboembolic pulmonary hypertension: a systematic review and meta-analysis
  42. Risk stratification and medical therapy of pulmonary arterial hypertension
  43. Germline BMP9 mutation causes idiopathic pulmonary arterial hypertension
  44. 3-Bromopyruvate Attenuates Experimental Pulmonary Hypertension via Inhibition of Glycolysis
  45. Percutaneous coronary intervention equates to placebo procedure in stable angina?
  46. When REVEAL meets AMBITION, does it reveal more?
  47. Increased risk of thrombosis in antiphospholipid syndrome patients treated with direct oral anticoagulants. Results from an international patient-level data meta-analysis
  48. Epigenetic Dysregulation of the Dynamin-Related Protein 1 Binding Partners MiD49 and MiD51 Increases Mitotic Mitochondrial Fission and Promotes Pulmonary Arterial Hypertension
  49. Inhibition of CRTH2-mediated Th2 activation attenuates pulmonary hypertension in mice
  50. Impact of Pituitary–Gonadal Axis Hormones on Pulmonary Arterial Hypertension in Men
  51. Metabolic reprogramming of the urea cycle pathway in experimental pulmonary arterial hypertension rats induced by monocrotaline
  52. Efficacy and safety of bivalirudin in coronary artery disease patients with mild to moderate chronic kidney disease: Meta-analysis
  53. IgG4-related disease of pulmonary artery causing pulmonary hypertension
  54. Whole-exome sequencing improves genetic testing accuracy in pulmonary artery hypertension
  55. Prognostic Significance of Reduced Blood Pressure Response to Exercise in Pediatric Pulmonary Arterial Hypertension
  56. Hemodynamic and gas exchange effects of inhaled iloprost in patients with COPD and pulmonary hypertension
  57. Hypermethylation of BMPR2 Promoter Occurs in Patients with Heritable Pulmonary Arterial Hypertension and Inhibits BMPR2 Expression
  58. Macitentan for the treatment of inoperable chronic thromboembolic pulmonary hypertension (MERIT-1): results from the multicentre, phase 2, randomised, double-blind, placebo-controlled study
  59. Reply to “Comment on direct bilirubin as predictor of severity and mortality in idiopathic pulmonary arterial hypertension”
  60. Enhancing Insights into Pulmonary Vascular Disease through a Precision Medicine Approach. A Joint NHLBI–Cardiovascular Medical Research and Education Fund Workshop Report
  61. A novel scoring index by Doppler echocardiography for predicting severe pulmonary hypertension due to chronic lung diseases: a cross-sectional diagnostic accuracy study
  62. Comparison of hemodynamic parameters in treatment-naïve and pre-treated patients with pulmonary arterial hypertension in the randomized phase III PATENT-1 study
  63. Riociguat: a soluble guanylate cyclase stimulator for the treatment of pulmonary hypertension
  64. Efficacy of 1, 5, and 20 mg oral sildenafil in the treatment of adults with pulmonary arterial hypertension: a randomized, double-blind study with open-label extension
  65. Direct bilirubin: A new risk factor of adverse outcome in idiopathic pulmonary arterial hypertension
  66. Cysteine-rich 61 (Cyr61) upregulated in pulmonary arterial hypertension promotes the proliferation of pulmonary artery smooth muscle cells
  67. Cardiopulmonary exercise testing improves diagnostic specificity in patients with echocardiography-suspected pulmonary hypertension
  68. Elevated levels of plasma transforming growth factor-β1 in idiopathic and heritable pulmonary arterial hypertension
  69. Optical coherence tomography for hypertensive pulmonary vasculature
  70. Evaluation of efficacy, safety and tolerability of Ambrisentan in Chinese adults with pulmonary arterial hypertension: a prospective open label cohort study
  71. Energetic Metabolic Roles in Pulmonary Arterial Hypertension and Right Ventricular Remodeling
  72. Profiling nitric oxide metabolites in patients with idiopathic pulmonary arterial hypertension
  73. Clinical characteristics of pulmonary hypertension in bronchiectasis
  74. Elevated Levels of Circulating Bone Morphogenetic Protein 7 Predict Mortality in Pulmonary Arterial Hypertension
  75. Identifying microRNAs targeting Wnt/β-catenin pathway in end-stage idiopathic pulmonary arterial hypertension
  76. BMPR2 mutation is a potential predisposing genetic risk factor for congenital heart disease associated pulmonary vascular disease
  77. Predictors of long-term outcomes in patients treated with riociguat for pulmonary arterial hypertension: data from the PATENT-2 open-label, randomised, long-term extension trial
  78. Riociguat for the treatment of pulmonary hypertension: Chinese subgroup analyses and comparison
  79. A global view of pulmonary hypertension
  80. Shape of the Pulmonary Artery Doppler-Flow Profile Predicts the Hemodynamics of Pulmonary Hypertension Caused by Left-Sided Heart Disease
  81. Acute Vasodilator Response in Pediatric Pulmonary Arterial Hypertension
  82. Effect of intravenous l-carnitine in Chinese patients with chronic heart failure
  83. BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis
  84. Reversal of right ventricular remodeling by dichloroacetate is related to inhibition of mitochondria-dependent apoptosis
  85. Review Common genetic risk factors of venous thromboembolism in Western and Asian populations
  86. Haemodynamic characterisation and heart catheterisation complications in children with pulmonary hypertension: Insights from the Global TOPP Registry (tracking outcomes and practice in paediatric pulmonary hypertension)
  87. The limits of oral therapy in pulmonary arterial hypertension management
  88. Research update for articles published in EJCI in 2013
  89. Effects of oral treatments on clinical outcomes in pulmonary arterial hypertension: A systematic review and meta-analysis
  90. Intravenous fasudil improves in-hospital mortality of patients with right heart failure in severe pulmonary hypertension
  91. Riociguat for the treatment of pulmonary arterial hypertension: a long-term extension study (PATENT-2)
  92. Bosentan up-front or sequential add-on combination treatment for pulmonary arterial hypertension: long-term effects and prognosis
  93. Isoprostane as a promising biomarker in pulmonary arterial hypertension: Preanalytical and analytical viewpoints. Response to letter to the editor
  94. Acute hemodynamic response of infused fasudil in patients with pulmonary arterial hypertension: A randomized, controlled, crossover study
  95. Frequency of Supraventricular Arrhythmias in Patients With Idiopathic Pulmonary Arterial Hypertension
  96. Up-regulation of hexokinase1 in the right ventricle of monocrotaline induced pulmonary hypertension
  97. Plasma 15-F2t-isoprostane in idiopathic pulmonary arterial hypertension
  98. Connective tissue disease-associated pulmonary arterial hypertension in Chinese patients
  99. BMPR2 Germline Mutation in Chronic Thromboembolic Pulmonary Hypertension
  100. Rivaroxaban for the treatment of symptomatic deep-vein thrombosis and pulmonary embolism in Chinese patients: a subgroup analysis of the EINSTEIN DVT and PE studies
  101. Updated Treatment Algorithm of Pulmonary Arterial Hypertension
  102. Pediatric Pulmonary Arterial Hypertension
  103. Epidemiology of Pulmonary Arterial Hypertension
  104. Oral Treprostinil for the Treatment of Pulmonary Arterial Hypertension in Patients Receiving Background Endothelin Receptor Antagonist and Phosphodiesterase Type 5 Inhibitor Therapy (The FREEDOM-C2 Study)
  105. Macitentan and Morbidity and Mortality in Pulmonary Arterial Hypertension
  106. Antioxidant effects of phosphodiesterase-5 inhibitors: reply
  107. Clinical and genetic characteristics of Chinese patients with hereditary haemorrhagic telangiectasia-associated pulmonary hypertension
  108. Riociguat for the Treatment of Pulmonary Arterial Hypertension
  109. Complexities of oestradiol pharmacology in pulmonary arterial hypertension
  110. The phosphodiesterase-5 inhibitor vardenafil reduces oxidative stress while reversing pulmonary arterial hypertension
  111. Efficacy and Safety of Oral Treprostinil Monotherapy for the Treatment of Pulmonary Arterial Hypertension
  112. Lower Socioeconomic Status Is Associated with Worse Outcomes in Pulmonary Arterial Hypertension
  113. BMPR2Mutations Influence Phenotype More Obviously in Male Patients With Pulmonary Arterial Hypertension
  114. Oestradiol ameliorates monocrotaline pulmonary hypertensionviaNO, prostacyclin and endothelin-1 pathways
  115. Serum High-Density Lipoprotein Cholesterol Levels as a Prognostic Indicator in Patients With Idiopathic Pulmonary Arterial Hypertension
  116. Usefulness of Intravenous Adenosine in Idiopathic Pulmonary Arterial Hypertension as a Screening Agent for Identifying Long-Term Responders to Calcium Channel Blockers
  117. Clinical features of paediatric pulmonary hypertension: a registry study
  118. Prolonged QRS Duration
  119. High-Altitude Pulmonary Hypertension
  120. Idiopathic Pulmonary Arterial Hypertension and Its Prognosis in the Modern Management Era in Developed and Developing Countries
  121. MicroRNA-134 as a potential plasma biomarker for the diagnosis of acute pulmonary embolism
  122. Oral sildenafil treatment for Eisenmenger syndrome: a prospective, open-label, multicentre study
  123. Survival of Chinese Patients With Pulmonary Arterial Hypertension in the Modern Treatment Era
  124. Molecular genetics and clinical features of Chinese idiopathic and heritable pulmonary arterial hypertension patients
  125. Vardenafil in Pulmonary Arterial Hypertension
  126. Iloprost—different indications and different national experiences in treating pulmonary hypertension
  127. Survival in incident and prevalent cohorts of patients with pulmonary arterial hypertension
  128. Efficacy, safety and tolerability of bosentan in Chinese patients with pulmonary arterial hypertension
  129. Pulmonary function testing in patients with pulmonary arterial hypertension
  130. The efficacy and safety of sildenafil in Chinese patients with pulmonary arterial hypertension
  131. Vardenafil treatment for patients with pulmonary arterial hypertension: a multicentre, open-label study
  132. Updated Clinical Classification of Pulmonary Hypertension
  133. High-altitude pulmonary hypertension
  134. Iloprost for pulmonary vasodilator testing in idiopathic pulmonary arterial hypertension
  135. Hemodynamic variables and clinical features correlated with serum uric acid in patients with pulmonary arterial hypertension
  136. Registry and Survival Study in Chinese Patients With Idiopathic and Familial Pulmonary Arterial Hypertension
  137. Post-infarction treatment with simvastatin reduces myocardial no-reflow by opening of the KATPchannel
  138. Complications of Right Heart Catheterization Procedures in Patients With Pulmonary Hypertension in Experienced Centers
  139. Different effects of tirofiban and aspirin plus clopidogrel on myocardial no-reflow in a mini-swine model of acute myocardial infarction and reperfusion
  140. Pretreatment with fosinopril or valsartan reduces myocardial no-reflow after acute myocardial infarction and reperfusion
  141. Herpes Simplex Virus Type 2 Infection Is a Risk Factor for Hypertension