All Stories

  1. Bridging Disciplines in Portopulmonary Hypertension: A Multidisciplinary Call for Harmonized Patient Management
  2. Chronic thromboembolic pulmonary hypertension associated with venous thoracic outlet syndrome: a retrospective case series
  3. Correspondence on: Pulmonary arterial hypertension in adults with Still’s disease: another pulmonary manifestation associated with HLA-DRB1*15–reply
  4. Response to correspondence on: Pulmonary arterial hypertension in adults with Still's disease: another pulmonary manifestation associated with HLA-DRB1*15
  5. Safety and Efficacy of upfront triple therapy including parenteral treprostinil compared to double oral therapy in PAH (TripleTRE): study protocol for a randomized trial
  6. Seralutinib for the Treatment of Pulmonary Arterial Hypertension in Adults: TORREY Open-Label Extension Study
  7. Clustering Patients with Pulmonary Hypertension Using the Plasma Proteome
  8. The Activin Pathway in Chronic Thromboembolic Pulmonary Hypertension: A Potential Biomarker for Residual Pulmonary Hypertension After Endarterectomy
  9. Diuretic adherence in patients with precapillary pulmonary hypertension: insights from the PHARE study
  10. Drugs targeting novel pathways in pulmonary arterial hypertension
  11. Risk stratification in Eisenmenger syndrome
  12. ERS Congress 2024: highlights from the Pulmonary Vascular Diseases Assembly
  13. Effect of Balloon Pulmonary Angioplasty and Riociguat on Right Ventricular Afterload and Function in CTEPH: Insights From the RACE Trial
  14. Changes in REVEAL Lite 2 risk status are associated with long-term outcomes in patients with pulmonary arterial hypertension: A post-hoc analysis of the GRIPHON study
  15. Effect of sotatercept on circulating proteomics in pulmonary arterial hypertension
  16. Thirty years of surgical management of pediatric pulmonary hypertension: Mid-term outcomes following reverse Potts shunt and transplantation
  17. Treatment algorithm for pulmonary arterial hypertension
  18. Medication adherence, related factors and outcomes among patients with pulmonary arterial hypertension or chronic thromboembolic pulmonary hypertension: a systematic review
  19. Risk Assessment in Pulmonary Veno-Occlusive Disease: The First Step Towards Future Trials?
  20. Percutaneous atrial septal defect closure in patients with pulmonary arterial hypertension
  21. POINT: Should the Use of Upfront Triple Combination Therapy Be Standard of Care in Pulmonary Arterial Hypertension? Yes
  22. Pulmonary veno-occlusive disease: illustrative cases and literature review
  23. The Management of Pulmonary Arterial Hypertension in the Setting of Systemic Sclerosis
  24. From the microscopic to the macroscopic: clinical–radiological–pathological correlation in pulmonary hypertension
  25. ERS International Congress 2023: highlights from the Pulmonary Vascular Diseases Assembly
  26. Sequential multimodal therapy in chronic thromboembolic pulmonary hypertension with mixed anatomical lesions: a proof of concept
  27. Pulmonary arterial hypertension
  28. Diagnosis and management of pulmonary veno-occlusive disease
  29. New trends in pulmonary hypertension
  30. Reply to Jha
  31. The Influence of Methods for Cardiac Output Determination on the Diagnosis of Precapillary Pulmonary Hypertension: A Mathematical Model
  32. To be or not to be… treated with initial combination therapy, that is the (PAH) question
  33. Erythrocytes are altered in pulmonary arterial hypertension
  34. ERS statement on chronic thromboembolic pulmonary hypertension
  35. Sequential combination therapy with parenteral prostacyclin in BMPR2 mutations carriers
  36. Reply to Jin et al. and to Sun et al.
  37. Sex and gender in pulmonary arterial hypertension
  38. Outcomes of patients with decreased arterial oxyhaemoglobin saturation on pulmonary arterial hypertension drugs
  39. The isobaric pulmonary arterial compliance in pulmonary hypertension
  40. Pulmonary Vascular Resistance in Pulmonary Arterial Hypertension: La Pièce de Résistance?
  41. Initial triple therapy in pulmonary arterial hypertension: coming of age and rejuvenated
  42. Reply to: “Management of portopulmonary hypertension: What is more important, PAH severity or liver disease severity?”
  43. ERS statement on chronic thromboembolic pulmonary hypertension
  44. Reversible pulmonary hypertension associated with multivisceral Whipple's disease
  45. Long-term outcomes with initial triple oral therapy in pulmonary arterial hypertension (PAH): Insights from TRITON
  46. Pulmonary Hypertension Complicating Pulmonary Artery Involvement in Pseudoxanthoma Elasticum
  47. Pulmonary complications of Bcr-Abl tyrosine kinase inhibitors
  48. Severe Pulmonary Hypertension Management Across Europe (PHAROS): an ERS Clinical Research Collaboration
  49. Initial combination therapy of macitentan and tadalafil in pulmonary arterial hypertension
  50. Transition from intravenous epoprostenol to selexipag in pulmonary arterial hypertension: a word of caution
  51. Pulmonary arterial hypertension registries: past, present and into the future
  52. Intensity and quality of exertional dyspnoea in patients with stable pulmonary hypertension
  53. A dynamic prognostic model to predict survival and determine treatment goals in pulmonary arterial hypertension (PAH): the EFORT study
  54. Assembly 13: placing the pulmonary circulation in the heart of ERS
  55. Highlights from the ERS International Congress 2018: Assembly 13 – Pulmonary Vascular Diseases
  56. Clinical trial design and new therapies for pulmonary arterial hypertension
  57. Hépatopathies et maladies vasculaires pulmonaires
  58. Clinical and Hemodynamic Correlates of Pulmonary Arterial Stiffness in Incident, Untreated Patients With Idiopathic Pulmonary Arterial Hypertension
  59. Association Between BMI and Obesity With Survival in Pulmonary Arterial Hypertension
  60. Impact of the initiation of balloon pulmonary angioplasty program on referral of patients with chronic thromboembolic pulmonary hypertension to surgery
  61. Risk stratification in pulmonary arterial hypertension
  62. Évaluation de l’IRM cardiaque dans le suivi des patients ayant une hypertension artérielle pulmonaire (EVITA). IRM cardiaque dans le suivi de l’hypertension artérielle pulmonaire
  63. Pulmonary hypertension associated with neurofibromatosis type 1
  64. Natural History over 8 Years of Pulmonary Vascular Disease in a Patient Carrying Biallelic EIF2AK4 Mutations
  65. Pharmacovigilance in a rare disease: example of the VIGIAPATH program in pulmonary arterial hypertension
  66. Portopulmonary hypertension
  67. Factors predicting outcome after pulmonary endarterectomy
  68. Genetic determinants of risk and survival in pulmonary arterial hypertension
  69. Clinical phenotypes and survival of pre-capillary pulmonary hypertension in systemic sclerosis
  70. Age, risk and outcomes in idiopathic pulmonary arterial hypertension
  71. Pulmonary vascular remodeling patterns and expression of general control nonderepressible 2 (GCN2) in pulmonary veno-occlusive disease
  72. The Low-Risk Profile in Pulmonary Arterial Hypertension. Time for a Paradigm Shift to Goal-oriented Clinical Trial Endpoints?
  73. Outcome of Portopulmonary Hypertension After Liver Transplantation
  74. Association between six-minute walk distance and long-term outcomes in patients with pulmonary arterial hypertension: Data from the randomized SERAPHIN trial
  75. Risk assessment in pulmonary arterial hypertension
  76. Temporary treatment interruptions with oral selexipag in pulmonary arterial hypertension: Insights from the Prostacyclin (PGI 2 ) Receptor Agonist in Pulmonary Arterial Hypertension (GRIPHON) study
  77. Prognostic Value of Follow-Up Hemodynamic Variables After Initial Management in Pulmonary Arterial Hypertension
  78. RV Fractional Area Change and TAPSE as Predictors of Severe Right Ventricular Dysfunction in Pulmonary Hypertension: A CMR Study
  79. Pulmonary Arterial Hypertension-Related Morbidity Is Prognostic for Mortality
  80. La maladie veino-occlusive pulmonaire
  81. Targeting the Prostacyclin Pathway with Selexipag in Patients with Pulmonary Arterial Hypertension Receiving Double Combination Therapy: Insights from the Randomized Controlled GRIPHON Study
  82. Association between Rheumatoid Arthritis and Pulmonary Hypertension: Data from the French Pulmonary Hypertension Registry
  83. Pulmonary Arterial Hypertension Associated With Systemic Lupus Erythematosus
  84. Acute decompensated pulmonary hypertension
  85. Dead-space ventilation is linked to exercise capacity and survival in distal chronic thromboembolic pulmonary hypertension
  86. Management and long-term outcomes of sarcoidosis-associated pulmonary hypertension
  87. Medical Treatment of Pulmonary Arterial Hypertension
  88. Portopulmonary Hypertension
  89. Exertional dyspnoea in pulmonary arterial hypertension
  90. Are indexed values better for defining exercise pulmonary hypertension?
  91. Plasma proteome analysis in patients with pulmonary arterial hypertension: an observational cohort study
  92. Risk assessment, prognosis and guideline implementation in pulmonary arterial hypertension
  93. Selexipag for the treatment of connective tissue disease-associated pulmonary arterial hypertension
  94. Impact of High-Priority Allocation on Lung and Heart-Lung Transplantation for Pulmonary Hypertension
  95. Long-term outcomes of dasatinib-induced pulmonary arterial hypertension: a population-based study
  96. Validation of a risk assessment instrument for pulmonary arterial hypertension
  97. Pulmonary hypertension due to left heart disease
  98. Outcome of adults with Eisenmenger syndrome treated with drugs specific to pulmonary arterial hypertension: A French multicentre study
  99. Long-term outcomes of pulmonary arterial hypertension under specific drug therapy in Eisenmenger syndrome
  100. Ambrisentan use for pulmonary arterial hypertension in a post-authorization drug registry: The VOLibris Tracking Study
  101. Long-term outcome in liver transplantation candidates with portopulmonary hypertension
  102. Gut–Lung Connection in Pulmonary Arterial Hypertension
  103. SERAPHIN haemodynamic substudy: the effect of the dual endothelin receptor antagonist macitentan on haemodynamic parameters and NT-proBNP levels and their association with disease progression in patients with pulmonary arterial hypertension
  104. Clinical phenotypes and outcomes of heritable and sporadic pulmonary veno-occlusive disease: a population-based study
  105. Epoprostenol and pulmonary arterial hypertension: 20 years of clinical experience
  106. Macitentan Improves Health-Related Quality of Life for Patients With Pulmonary Arterial Hypertension
  107. Proceedings of Réanimation 2017, the French Intensive Care Society International Congress
  108. A Clinical and Echocardiographic Score to Identify Pulmonary Hypertension Due to HFpEF
  109. Beyond a single pathway: combination therapy in pulmonary arterial hypertension
  110. BMPR2mutation status influences bronchial vascular changes in pulmonary arterial hypertension
  111. Deterioration of pulmonary hypertension and pleural effusion with bosutinib following dasatinib lung toxicity
  112. Interferon-induced pulmonary hypertension
  113. Pulmonary arterial hypertension in idiopathic inflammatory myopathies
  114. Non-invasive diagnosis of pulmonary hypertension from lung Doppler signal: a proof of concept study
  115. Dasatinib induces lung vascular toxicity and predisposes to pulmonary hypertension
  116. Direct-Acting Antiviral Medications for Hepatitis C Virus Infection and Pulmonary Arterial Hypertension
  117. International Liver Transplant Society Practice Guidelines
  118. Regulatory T Cell Dysfunction in Idiopathic, Heritable and Connective Tissue-Associated Pulmonary Arterial Hypertension
  119. Lung capillary blood volume and membrane diffusion in precapillary pulmonary hypertension
  120. Response to Letter Regarding Article, “Mitomycin-Induced Pulmonary Veno-Occlusive Disease: Evidence From Human Disease and Animal Model”
  121. Diagnostic concordance of different criteria for exercise pulmonary hypertension in subjects with normal resting pulmonary artery pressure
  122. Pulmonary veno-occlusive disease
  123. Initial dual oral combination therapy in pulmonary arterial hypertension
  124. Resting pulmonary artery pressure of 21–24 mmHg predicts abnormal exercise haemodynamics
  125. A rare case of sarcoidosis-associated pulmonary hypertension in a patient exposed to silica
  126. Patients’, relatives’, and practitioners’ views of pulmonary arterial hypertension: A qualitative study
  127. BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis
  128. Loss of Vascular Distensibility During Exercise Is an Early Hemodynamic Marker of Pulmonary Vascular Disease
  129. Comparative Safety and Tolerability of Prostacyclins in Pulmonary Hypertension
  130. Kinetics of Cardiac Output at the Onset of Exercise in Precapillary Pulmonary Hypertension
  131. Infections liées aux cathéters veineux centraux tunnélisés chez les patients ayant une hypertension artérielle pulmonaire traitée par prostacycline intraveineuse
  132. Selexipag for the Treatment of Pulmonary Arterial Hypertension
  133. Genetic counselling in a national referral centre for pulmonary hypertension
  134. Usefulness of Cardiovascular Magnetic Resonance Indices to Rule In or Rule Out Precapillary Pulmonary Hypertension
  135. Chronic thromboembolic pulmonary hypertension
  136. Pulmonary arterial hypertension in patients treated with interferon: TABLE 1
  137. Occupational exposure to organic solvents: a risk factor for pulmonary veno-occlusive disease
  138. Pulmonary Hypertension Complicating Fibrosing Mediastinitis
  139. Incident and prevalent cohorts with pulmonary arterial hypertension: insight from SERAPHIN
  140. The 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: a practical chronicle of progress
  141. Response to Letter Regarding Article, “Advances in Therapeutic Interventions for Patients With Pulmonary Arterial Hypertension”
  142. Mitomycin-Induced Pulmonary Veno-Occlusive Disease
  143. A prospective study of the 6 min walk test as a surrogate marker for haemodynamics in two independent cohorts of treatment-naïve systemic sclerosis-associated pulmonary arterial hypertension
  144. New pharmacotherapy options for pulmonary arterial hypertension
  145. Non-Invasive Determination of Cardiac Output in Pre-Capillary Pulmonary Hypertension
  146. Nasal decongestant exposure in patients with pulmonary arterial hypertension: a pilot study: TABLE 1
  147. Criteria for diagnosis of exercise pulmonary hypertension
  148. Characteristics of Pulmonary Arterial Hypertension in Affected Carriers of a Mutation Located in the Cytoplasmic Tail of Bone Morphogenetic Protein Receptor Type 2
  149. Inspiratory muscle function, dynamic hyperinflation and exertional dyspnoea in pulmonary arterial hypertension
  150. Validation of two predictive models for survival in pulmonary arterial hypertension
  151. Systolic and Mean Pulmonary Artery Pressures
  152. Relation between left ventricular ejection time and pulmonary hemodynamics in pulmonary hypertension
  153. Chemotherapy-Induced Pulmonary Hypertension
  154. Effect of Macitentan on Hospitalizations
  155. Advances in Therapeutic Interventions for Patients With Pulmonary Arterial Hypertension
  156. Connective tissue disease associated with pulmonary arterial hypertension: management of a patient with severe haemodynamic impairment
  157. Pulmonary arterial hypertension
  158. Clinical Pharmacology of Endothelin Receptor Antagonists Used in the Treatment of Pulmonary Arterial Hypertension
  159. Pulmonary arterial hypertension in patients treated with interferon
  160. Lung and heart-lung transplantation for systemic sclerosis patients. A monocentric experience of 13 patients, review of the literature and position paper of a multidisciplinary Working Group
  161. Hypertension pulmonaire et maladies hépatiques
  162. Traitement chirurgical de l’hypertension pulmonaire post-embolique
  163. Traitement de l’hypertension artérielle pulmonaire
  164. Mechanisms of exertional dyspnoea in pulmonary veno-occlusive disease with EIF2AK4 mutations
  165. Long-term sildenafil added to intravenous epoprostenol in patients with pulmonary arterial hypertension
  166. Prognostic value of exercise pulmonary haemodynamics in pulmonary arterial hypertension
  167. The potential for macitentan, a new dual endothelin receptor antagonist, in the treatment of pulmonary arterial hypertension
  168. Current epoprostenol use in patients with severe idiopathic, heritable or anorexigen-associated pulmonary arterial hypertension: Data from the French pulmonary hypertension registry
  169. Biomarkers for the prognosis of pulmonary arterial hypertension: Holy grail or flying circus?
  170. Upfront triple combination therapy in pulmonary arterial hypertension: a pilot study
  171. EPITOME-2: An open-label study assessing the transition to a new formulation of intravenous epoprostenol in patients with pulmonary arterial hypertension
  172. Right heart failure: Toward a common language
  173. Targeted therapies in pulmonary arterial hypertension
  174. EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension
  175. Treatment Goals of Pulmonary Hypertension
  176. Proinflammatory cytokine levels are linked to death in pulmonary arterial hypertension
  177. Left Ventricular Ejection Time in Acute Heart Failure Complicating Precapillary Pulmonary Hypertension
  178. Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy
  179. Inflammatory Mechanisms in HIV-Associated Pulmonary Arterial Hypertension
  180. Macitentan and Morbidity and Mortality in Pulmonary Arterial Hypertension
  181. Pharmacokinetic evaluation of sildenafil as a pulmonary hypertension treatment
  182. Pulmonary arterial hypertension
  183. Calcium-Channel Blockers in Pulmonary Arterial Hypertension
  184. Pathways in pulmonary arterial hypertension: the future is here
  185. Survival in systemic sclerosis-associated pulmonary arterial hypertension in the modern management era
  186. Independent Association of Urinary F2-Isoprostanes With Survival in Pulmonary Arterial Hypertension
  187. Pulmonary veno-occlusive disease and pulmonary capillary haemangiomatosis
  188. Hemodynamics in Pulmonary Arterial Hypertension: Current and Future Perspectives
  189. The study of risk in pulmonary arterial hypertension
  190. Treat-to-target approach in pulmonary arterial hypertension: a consensus-based proposal
  191. Computed tomography findings of pulmonary venoocclusive disease in scleroderma patients presenting with precapillary pulmonary hypertension
  192. Renal Replacement Therapy in Patients with Severe Precapillary Pulmonary Hypertension with Acute Right Heart Failure
  193. Out-of-Proportion Pulmonary Hypertension and Heart Failure with Preserved Ejection Fraction
  194. Dynamic respiratory mechanics and exertional dyspnoea in pulmonary arterial hypertension
  195. EBUS-TBNA in the differential diagnosis of pulmonary artery sarcoma and thromboembolism: Figure 1–
  196. Efficacy, safety and pharmacokinetics of bosentan in portopulmonary hypertension
  197. Pulmonary Arterial Hypertension in Patients Treated by Dasatinib
  198. Mediastinal Fibrosis Mimicking Proximal Chronic Thromboembolic Disease
  199. Pulmonary hypertension associated with benfluorex exposure
  200. Portopulmonary Hypertension
  201. L’hypertension artérielle pulmonaire associée au VIH
  202. Usefulness of first-line combination therapy with epoprostenol and bosentan in pulmonary arterial hypertension: An observational study
  203. Portopulmonary Hypertension and Hepatopulmonary Syndrome
  204. Optimal management of severe pulmonary arterial hypertension
  205. Systemic lupus erythematosus-associated PAH: is targeting inflammation the key to success?
  206. Ventilation/perfusion lung scan in pulmonary veno-occlusive disease
  207. Screening for pulmonary arterial hypertension in patients with systemic sclerosis: Clinical characteristics at diagnosis and long-term survival
  208. Pulmonary Arterial Hypertension in a Patient With Cowden Syndrome and Anorexigen Exposure
  209. Systemic sclerosis-related pulmonary hypertension associated with interstitial lung disease: Impact of pulmonary arterial hypertension therapies
  210. Treatment of pulmonary arterial hypertension with targeted therapies
  211. The association between resting and mild-to-moderate exercise pulmonary artery pressure
  212. Pulmonary hypertension related to appetite suppressants
  213. Pulmonary Hypertension in Patients With Neurofibromatosis Type I
  214. Endothelin receptor antagonists for the treatment of pulmonary arterial hypertension
  215. Prise en charge de l’hypertension artérielle pulmonaire en 2011 : les innovations depuis les recommandations ERS/ESC 2009
  216. Pulmonary veno-occlusive disease: The bête noire of pulmonary hypertension in connective tissue diseases?
  217. Current management approaches to portopulmonary hypertension
  218. Pulmonary arterial hypertension: combination therapy in the modern management era
  219. Treat-to-target strategies in pulmonary arterial hypertension: the importance of using multiple goals
  220. Pharmacokinetic evaluation of continuous intravenous epoprostenol
  221. Effects of HIV Protease Inhibitors on Progression of Monocrotaline- and Hypoxia-Induced Pulmonary Hypertension in Rats
  222. Evidence for the use of combination targeted therapeutic approaches for the management of pulmonary arterial hypertension
  223. Pulmonary veno-occlusive disease: Recent progress and current challenges
  224. Survival in Patients With Idiopathic, Familial, and Anorexigen-Associated Pulmonary Arterial Hypertension in the Modern Management Era
  225. Survival in incident and prevalent cohorts of patients with pulmonary arterial hypertension
  226. Long-term response to calcium-channel blockers in non-idiopathic pulmonary arterial hypertension
  227. Absence of influence of gender and BMPR2 mutation type on clinical phenotypes of pulmonary arterial hypertension
  228. Objectifs thérapeutiques dans l’hypertension artérielle pulmonaire
  229. Characterization of Pulmonary Arterial Hypertension Patients Walking More Than 450 m in 6 Min at Diagnosis
  230. Assessing effectiveness of pulmonary arterial hypertension therapies in daily practice
  231. Clinical Outcomes of Pulmonary Arterial Hypertension in Patients Carrying anACVRL1(ALK1) Mutation
  232. Pulmonary arterial hypertension associated with systemic sclerosis in patients with functional class II dyspnoea: mild symptoms but severe outcome
  233. Diagnostic et prise en charge de l’hypertension pulmonaire en 2009. Commentaires sur les nouvelles recommandations de l’European Society of Cardiology (ESC) et de l’European Respiratory Society (ERS)
  234. HIV-associated pulmonary arterial hypertension: survival and prognostic factors in the modern therapeutic era
  235. Maladie veino-occlusive et hémangiomatose capillaire pulmonaire
  236. Long-term outcome of systemic sclerosis-associated pulmonary arterial hypertension treated with bosentan as first-line monotherapy followed or not by the addition of prostanoids or sildenafil
  237. Implementing the ESC/ERS pulmonary hypertension guidelines: real-life cases from a national referral centre
  238. Prognostic factors of acute heart failure in patients with pulmonary arterial hypertension
  239. Noncardiothoracic nonobstetric surgery in mild-to-moderate pulmonary hypertension
  240. Is Pulmonary Arterial Hypertension Really a Late Complication of Systemic Sclerosis?
  241. Goal-oriented therapy in pulmonary veno-occlusive disease: a word of caution
  242. Pulmonary Venoocclusive Disease and Failure of Specific Therapy
  243. Phosphodiesterase type 5 inhibitors in pulmonary arterial hypertension
  244. Fatal dissection of the pulmonary artery in pulmonary arterial hypertension
  245. Idiopathic Pulmonary Arterial Hypertension and Pulmonary Veno-occlusive Disease: Similarities and Differences
  246. Pulmonary Arterial Hypertension and HIV Infection
  247. Intravenous iloprost for pulmonary arterial hypertension: still waiting for evidence
  248. Cautious epoprostenol therapy is a safe bridge to lung transplantation in pulmonary veno-occlusive disease
  249. The three-year incidence of pulmonary arterial hypertension associated with systemic sclerosis in a multicenter nationwide longitudinal study in France
  250. End Points and Clinical Trial Design in Pulmonary Arterial Hypertension
  251. Updated Evidence-Based Treatment Algorithm in Pulmonary Arterial Hypertension
  252. Cirrhosis ameliorates monocrotaline-induced pulmonary hypertension in rats
  253. Fenfluramine-like cardiovascular side-effects of benfluorex
  254. Pulmonary veno-occlusive disease
  255. Long-term effects of bosentan in patients with HIV-associated pulmonary arterial hypertension
  256. Addition of Sildenafil to Long-Term Intravenous Epoprostenol Therapy in Patients with Pulmonary Arterial Hypertension
  257. Risk factors for death and the 3-year survival of patients with systemic sclerosis: the French ItinerAIR-Sclerodermie study
  258. Portopulmonary Hypertension
  259. HIV-related pulmonary arterial hypertension: clinical presentation and management
  260. Review: Therapeutic advances in pulmonary arterial hypertension
  261. Pulmonary Veno-Occlusive Disease
  262. Clinical Outcomes of Pulmonary Arterial Hypertension in Carriers ofBMPR2Mutation
  263. Changes in exercise haemodynamics during treatment in pulmonary arterial hypertension
  264. Pulmonary arterial hypertension associated with fenfluramine exposure: report of 109 cases
  265. Immunosuppressive therapy in lupus- and mixed connective tissue disease–associated pulmonary arterial hypertension: A retrospective analysis of twenty-three cases
  266. Prevalence of HIV-related Pulmonary Arterial Hypertension in the Current Antiretroviral Therapy Era
  267. Intravenous Epoprostenol in Inoperable Chronic Thromboembolic Pulmonary Hypertension
  268. Hypertension pulmonaire postembolique
  269. Hypertension artérielle pulmonaire postembolique tumorale
  270. Pulmonary vascular abnormalities in cirrhosis
  271. Rapid Switch From Intravenous Epoprostenol to Intravenous Treprostinil in Patients With Pulmonary Arterial Hypertension
  272. Hypertension portopulmonaire
  273. Cœur pulmonaire chronique postembolique révélant une bêtathalassémie intermédiaire après splénectomie
  274. Bosentan for the treatment of pulmonary arterial hypertension associated with congenital heart defects
  275. Long term imatinib treatment in pulmonary arterial hypertension
  276. Immunosuppressive Therapy in Connective Tissue Diseases-Associated Pulmonary Arterial Hypertension
  277. Pulmonary Arterial Hypertension in France
  278. Mutations of the TGF-β type II receptorBMPR2 in pulmonary arterial hypertension
  279. Long-term outcome with first-line bosentan therapy in idiopathic pulmonary arterial hypertension
  280. Deleterious Effects of β-Blockers on Exercise Capacity and Hemodynamics in Patients With Portopulmonary Hypertension
  281. Heart rate responses during the 6-minute walk test in pulmonary arterial hypertension
  282. Occult alveolar haemorrhage in pulmonary veno-occlusive disease
  283. Clinical Challenges in Pulmonary Hypertension
  284. Pulmonary Endothelin-1 Clearance in Human Pulmonary Arterial Hypertension
  285. Splenectomy and chronic thromboembolic pulmonary hypertension
  286. Survival in patients with class III idiopathic pulmonary arterial hypertension treated with first line oral bosentan compared with an historical cohort of patients started on intravenous epoprostenol
  287. Reversibility of pulmonary arterial hypertension in HIV/HHV8-associated Castleman's disease
  288. Diagnostic et classification des hypertensions artérielles pulmonaires
  289. Génétique de l’hypertension artérielle pulmonaire: données récentes et applications pratiques
  290. Traitement chirurgical de la maladie thromboembolique pulmonaire chronique
  291. Les traitements de l’hypertension artérielle pulmonaire à l’heure de la T2A. Recommandations du groupe de travail “Maladies vasculaires pulmonaires” de la Société de pneumologie de langue française
  292. Traitement de l’hypertension artérielle pulmonaire
  293. Pulmonary hypertension associated with sarcoidosis: mechanisms, haemodynamics and prognosis
  294. Hypertension artérielle pulmonaire
  295. Human herpes virus 8 in HIV and non-HIV infected patients with pulmonary arterial hypertension in France
  296. Treatment of pulmonary arterial hypertension with bosentan: from pathophysiology to clinical evidence
  297. Long-Term Response to Calcium Channel Blockers in Idiopathic Pulmonary Arterial Hypertension
  298. Severe Pulmonary Hypertension during Pregnancy
  299. Bosentan therapy for pulmonary arterial hypertension
  300. Survival with first-line bosentan in patients with primary pulmonary hypertension
  301. Évaluation pronostique de biomarqueurs dans l’hypertension artérielle pulmonaire
  302. Bosentan for the Treatment of Human Immunodeficiency Virus–associated Pulmonary Arterial Hypertension
  303. Caractéristiques cliniques, hémodynamiques et génétiques de l’hypertension artérielle pulmonaire familiale
  304. Traitement de l'hypertension artérielle pulmonaire
  305. Treatment of Pulmonary Arterial Hypertension
  306. Pulmonary Hypertension:CT of the Chest in Pulmonary Venoocclusive Disease
  307. Diagnosis and differential assessment of pulmonary arterial hypertension
  308. Endothelin receptor antagonists in pulmonary arterial hypertension
  309. Prostanoid therapy for pulmonary arterial hypertension
  310. Prise en charge thérapeutique de l’hypertension porto-pulmonaire
  311. Automatic quantification of right ventricular function with gated blood pool SPECT
  312. Chronic thromboembolic pulmonary hypertension
  313. Traitement chirurgical de l’hypertension artérielle pulmonaire post-embolique
  314. Prise en charge thérapeutique de l’hypertension porto-pulmonaire
  315. Novel therapeutic perspectives in pulmonary arterial hypertension
  316. Effects of the Dual Endothelin Receptor Antagonist Bosentan in Patients With Pulmonary Arterial Hypertension
  317. Prognostic Factors for Survival in Human Immunodeficiency Virus–associated Pulmonary Arterial Hypertension
  318. BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives
  319. Primary pulmonary hypertension: Current therapy
  320. Inhaled Iloprost for Severe Pulmonary Hypertension
  321. Long-term intravenous epoprostenol infusion in primary pulmonary hypertension
  322. Pulmonary arterial hypertension and type-I glycogen-storage disease: the serotonin hypothesis
  323. Effects of beraprost sodium, an oral prostacyclin analogue, in patients with pulmonary arterial hypertension: a randomized, double-blind, placebo-controlled trial
  324. Pulmonary Arterial Hypertension: Thin-Section CT Predictors of Epoprostenol Therapy Failure
  325. Pulmonary Artery Pressure–Flow Relations after Prostacyclin in Primary Pulmonary Hypertension
  326. Hypertension artérielle pulmonaire associée aux connectivites
  327. Effects of the dual endothelin-receptor antagonist bosentan in patients with pulmonary hypertension: a randomised placebocontrolled study
  328. PATHOBIOLOGY OF PULMONARY HYPERTENSION
  329. RISK FACTORS FOR PULMONARY ARTERIAL HYPERTENSION
  330. Improvement of von Willebrand Factor Proteolysis After Prostacyclin Infusion in Severe Pulmonary Arterial Hypertension
  331. Imbalance between Platelet Vascular Endothelial Growth Factor and Platelet-derived Growth Factor in Pulmonary Hypertension
  332. Severe Pulmonary Hypertension in Histiocytosis X
  333. Short-term and long-term epoprostenol (prostacyclin) therapy in pulmonary hypertension secondary to connective tissue diseases: results of a pilot study
  334. Treatment of pulmonary hypertension secondary to connective tissue diseases
  335. Primary Pulmonary Hypertension Associated With the Use of Fenfluramine Derivatives
  336. Inhaled nitric oxide as a screening agent for safely identifying responders to oral calcium-channel blockers in primary pulmonary hypertension
  337. Treatment of Severe Pulmonary Hypertension Secondary to Connective Tissue Diseases With Continuous IV Epoprostenol (Prostacyclin)
  338. Pulmonary vascular disorders in portal hypertension
  339. Clinical Significance of the Pulmonary Vasodilator Response During Short-term Infusion of Prostacyclin in Primary Pulmonary Hypertension
  340. Increased interleukin-1 and interleukin-6 serum concentrations in severe primary pulmonary hypertension.
  341. Inhaled nitric oxide as a screening vasodilator agent in primary pulmonary hypertension. A dose-response study and comparison with prostacyclin.
  342. Pneumopathie aiguë tipidique
  343. Minocycline pneumonitis and eosinophilia. A report on eight patients
  344. Minocycline Pneumonitis and Eosinophilia
  345. Auranofin in steroid dependent asthma.
  346. Prostanoid Treatment for Pulmonary Arterial Hypertension