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  1. The Minimal Important Difference in Borg Dyspnea Score in Pulmonary Arterial Hypertension
  2. Quality of life in patients with chronic thromboembolic pulmonary hypertension
  3. Association Between Initial Oral Therapy and Outcomes in Systemic Sclerosis-Related Pulmonary Arterial Hypertension
  4. Prognostic Significance of Biomarkers in Pulmonary Arterial Hypertension
  5. Health-related Quality of Life and Survival in Pulmonary Arterial Hypertension
  6. Measuring Outcomes in Patients With Pulmonary Arterial Hypertension (PAH) Not on Active Treatment (MOTION): A Study of the Effects of Riociguat on Patient-Reported Outcomes and an Exploration of Telemetric Technology in PAH
  7. The minimal important difference of the epistaxis severity score in hereditary hemorrhagic telangiectasia
  8. Exercise Echocardiography in Connective Tissue Disease∗
  9. Right ventricular remodeling in idiopathic and scleroderma-associated pulmonary arterial hypertension: two distinct phenotypes
  10. Vascular Receptor Autoantibodies in Pulmonary Arterial Hypertension
  11. Sex Differences in Response to Tadalafil in Pulmonary Arterial Hypertension
  12. Severity of Systemic Sclerosis-Associated Pulmonary Arterial Hypertension in African Americans
  13. What Costs Can a U.S. Health Plan Expect if an Enrollee Has Chronic Thromboembolic Pulmonary Hypertension? A Guideline-Based Estimate of Healthcare Resource Use and Cost
  14. Guideline Based Estimates of Diagnostic and Treatment-Related Resource Use and Costs of a Typical Pulmonary Arterial Hypertension Patient to U.S. Health Plan
  15. Pulmonary Hypertension Associated with Connective Tissue Disease
  16. Chronic Expanding Hematoma of the Lung
  17. Recommendations for Screening and Detection of Connective Tissue Disease–Associated Pulmonary Arterial Hypertension
  18. Combined Pulmonary Fibrosis and Emphysema Among Patients With Scleroderma-Associated Pulmonary Hypertension
  19. A Look to the Past, Present, and Future of Pulmonary Hypertension
  20. Comparison of Moderate versus Deep Sedation for Endobronchial Ultrasound Transbronchial Needle Aspiration
  21. Reply: A Call to Apply the Minimal Important Difference in Pulmonary Arterial Hypertension beyond the Flawed 6-Minute-Walk Test
  22. Solvitur Ambulando…or Maybe Not?
  23. Development and validation of the living with pulmonary hypertension questionnaire in pulmonary arterial hypertension patients
  24. Regional and Global Biventricular Function in Pulmonary Arterial Hypertension: A Cardiac MR Imaging Study
  25. Pulmonary hypertension topics
  26. A Beginning’s End
  27. The Minimal Important Difference in the 6-Minute Walk Test for Patients with Pulmonary Arterial Hypertension
  28. Pulmonary Arterial Hypertension in Connective Tissue Diseases
  29. Pulmonary Arterial Hypertension: MR Imaging-derived First-Pass Bolus Kinetic Parameters Are Biomarkers for Pulmonary Hemodynamics, Cardiac Function, and Ventricular Remodeling
  30. Macrophage Migration Inhibitory Factor (MIF) Promoter Polymorphisms Are Associated With Favorable Hemodynamic Indices In Pulmonary Arterial Hypertension
  31. Gene Expression In The Neurohormonal Axis And Disease Severity In Treatment-Naive Scleroderma-Related Pulmonary Arterial Hypertension
  32. The Minimal Important Difference For The Six Minute Walk Test In Patients With Pulmonary Arterial Hypertension
  33. Epigenetic Regulations And Metabolic Abnormalities In Scleroderma-Associated Pulmonary Arterial Hypertension
  34. Cardiac MRI (cMRI) As A Screening Tool For Pulmonary Arterial Hypertension Associated With Systemic Sclerosis (PAH-SSc)
  35. Assessment Of Tricuspid Annular Plane Systolic Excursion (TAPSE) By 2D And M-Mode Echocardiography In Pulmonary Arterial Hypertension Patients
  36. The cost to managed care of managing pulmonary hypertension
  37. Increased Right Ventricular Septomarginal Trabeculation Mass is a Novel Marker for Pulmonary Hypertension
  38. Systemic sclerosis-related pulmonary hypertension associated with interstitial lung disease: Impact of pulmonary arterial hypertension therapies
  39. Serum Macrophage Migration Inhibitory Factor (MIF) Is Increased In Patients With Pulmonary Arterial Hypertension
  40. Exhaled Nitric Oxide In Scleroderma Patients Without Pulmonary Involvement
  41. Tricuspid Annular Plane Systolic Excursion In Idiopathic Versus Scleroderma-Related Pulmonary Arterial Hypertension
  42. The Relationship Between NT-ProBNP And Right Ventricular Function In Pulmonary Arterial Hypertension
  43. Bi-Ventricular Regional Function In Relation To Global Function And Hemodynamics In Pulmonary Hypertension: A Cardiac MRI Study
  44. Pulmonary Arterial Hypertension: First-Pass Contrast Bolus Kinetics Contain Information On RV Function, Remodeling, And Lung Resistance
  45. Pulmonary arterial hypertension associated with systemic sclerosis
  46. Myocardial Delayed Enhancement in Pulmonary Hypertension: Pulmonary Hemodynamics, Right Ventricular Function, and Remodeling
  47. Cardiac complications of systemic sclerosis: recent progress in diagnosis
  48. Is Pulmonary Arterial Hypertension Really a Late Complication of Systemic Sclerosis?
  49. Renal Dysfunction In Patients With Scleroderma-associated Pulmonary Arterial Hypertension: Severity And Impact On Outcomes
  50. The Impact Of Health-Related Quality Of Life On Outcomes In Pulmonary Arterial Hypertension
  51. Characteristics And Survival Of African-American Patients With Pulmonary Hypertension Associated With Scleroderma
  52. Epigenetic Modification Of Circulating Lymphocytes In Pulmonary Arterial Hypertension
  53. Effect Of Pulmonary Arterial Hypertension On Transcriptomics Of Peripheral Blood Mononuclear Cells
  54. Prognostic Value Of Percent Predicted Six Minute Walk Test Distance In Idiopathic Pulmonary Arterial Hypertension Patients: An Analysis Of The REVEAL Registry
  55. Combined Pulmonary Hypertension (PH) And Interstitial Lung Disease In Systemic Sclerosis: The Role Of PH Therapy
  56. Scleroderma Lung Disease
  57. Survival in Systemic Sclerosis–related Pulmonary Arterial Hypertension in the Modern Treatment Era
  58. Therapy for pulmonary arterial hypertension associated with systemic sclerosis
  59. Survival in pulmonary hypertension associated with the scleroderma spectrum of diseases: Impact of interstitial lung disease
  60. Sleep Quality and Health-Related Quality of Life in Idiopathic Pulmonary Fibrosis
  61. Hyponatremia Predicts Right Heart Failure and Poor Survival in Pulmonary Arterial Hypertension
  62. Identification of candidate genes in scleroderma-related pulmonary arterial hypertension
  63. Pulmonary Hypertension Related to Respiratory Disease
  64. Pulmonary Hypertension Associated with Chronic Respiratory Disease
  65. TRICUSPID ANNULAR PLANE SYSTOLIC EXCURSION PREDICTS MORTALITY IN PULMONARY ARTERIAL HYPERTENSION ASSOCIATED WITH SCLERODERMA
  66. Clinical differences between idiopathic and scleroderma-related pulmonary hypertension
  67. The Questionable Efficacy of Pirfenidone in IPF
  68. THE ADDITION OF SILDENAFIL TO BOSENTAN THERAPY IN THE TREATMENT OF PULMONARY ARTERIAL HYPERTENSION
  69. Long-Term Outcome of Bosentan Treatment in Idiopathic Pulmonary Arterial Hypertension and Pulmonary Arterial Hypertension Associated with the Scleroderma Spectrum of Diseases
  70. Faculty of 1000 evaluation for Iron deficiency is common in idiopathic pulmonary arterial hypertension.
  71. Faculty of 1000 evaluation for Impaired cardiac autonomic control relates to disease severity in pulmonary hypertension.
  72. Faculty of 1000 evaluation for Long-term outcome with intravenous iloprost in pulmonary arterial hypertension.
  73. Faculty of 1000 evaluation for Somatic chromosome abnormalities in the lungs of patients with pulmonary arterial hypertension.
  74. Faculty of 1000 evaluation for Riociguat for patients with pulmonary hypertension caused by systolic left ventricular dysfunction: a phase IIb double-blind, randomized, placebo-controlled, dose-ranging hemodynamic study.