Pulmonary hypertension (PH) is common and may result from a number of disorders,
including left heart disease, lung disease, and chronic thromboembolic disease. Pulmonary …

Importance Pulmonary arterial hypertension (PAH) is characterized by severe remodeling of
the distal pulmonary arteries, increased pulmonary vascular resistance, and right ventricular …

Pulmonary arterial hypertension (PAH) is a panvasculopathy that affects the distal
pulmonary arteries and leads to restricted blood flow. This increased afterload leads to …

Pulmonary arterial hypertension (PAH) is often difficult to diagnose and challenging to treat.
Untreated, it is characterized by a progressive increase in pulmonary vascular resistance …

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

Pulmonary arterial hypertension (PAH) is a rare disease, but one that continues to cause
significant morbidity and mortality despite much recent therapeutic progress. PAH is one …

Pulmonary hypertension (PH) describes a group of severe pulmonary vascular disorders
characterized by elevated mean pulmonary arterial pressure (mPAP) at rest. 1 The World …

Pulmonary arterial hypertension (PAH) is a term used to classify a variety of conditions that
have in common an injury to the pulmonary vasculature that produces elevations in …

Abstract Purpose of Review Pulmonary arterial hypertension (PAH) leads to progressive
increases in pulmonary vascular resistance (PVR), right heart failure, and death if left …

Pulmonary arterial hypertension (PAH) is diagnosed by various investigations that are
essential for making the diagnosis, and by additional tests to clarify the category of …