Importance Pulmonary arterial hypertension (PAH) is a subtype of pulmonary hypertension
(PH), characterized by pulmonary arterial remodeling. The prevalence of PAH is …

Since 1973 the World Symposia on Pulmonary Hypertension (WSPH) proceedings have
summarised the scientific advances and future needs in this field through the efforts of …

Pulmonary hypertension encompasses a range of conditions directly or indirectly leading to
elevated pressures within the pulmonary arteries. Five main groups of pulmonary …

Pulmonary hypertension (PH) is defined by a mean pulmonary artery pressure≥ 25 mm Hg
at rest, measured during right heart catheterization. There is still insufficient evidence to add …

Registries of patients with pulmonary arterial hypertension (PAH) have been instrumental in
characterizing the presentation and natural history of the disease and provide a basis for …

Patients with pulmonary hypertension associated with congenital heart disease make up an
increasing proportion of the total pulmonary hypertension population who bring with them …

Pulmonary arterial hypertension (PAH) is no longer an orphan disease. There are three
different classes of drugs for the treatment of PAH that are currently being used and an …

Although a substantial amount of information about clinical pulmonary arterial hypertension
(PAH) has accumulated over the past decades, there remains a need for our understanding …

Pulmonary hypertension (PH) is defined as mean pulmonary arterial pressure(PAP)
measured by right heart catheterization of 25 mm Hg or higher at rest. 1 The most recent …

Background: Left main coronary artery (LMCA) compression is increasingly recognized as a
cause of angina in pulmonary arterial hypertension (PAH). Objectives: This study aimed to …