Lysosomal dysfunction and inflammatory sterol metabolism in pulmonary arterial hypertension
ZENITH trial & a long-term follow-up study of Sotatercept for treatment of Pulmonary Arterial Hypertension: Interim results of SOTERIA. Our Community Call host Katrina Barry, participant in the long-term follow-up study of SOTERIA, joined the discussion with Aaron Waxman to answer any patient-related audience questions
Defining echocardiographic degrees of right heart size and function in pulmonary vascular disease from the PVDOMICS study
Skeletal muscle SIRT3 deficiency contributes to pulmonary vascular remodeling in pulmonary hypertension due to heart failure with preserved ejection fraction
Digital spatial profiling identifies distinct molecular signatures of vascular lesions in PAH
Phosphodiesterase-5 inhibitor treatment is associated with improved survival in pulmonary hypertension associated with COPD in the PVRI GoDeep meta-registry