Pulmonary hypertension is defined as a resting mean pulmonary artery pressure of 25 mm
Hg or above. This review deals with pulmonary arterial hypertension (PAH), a type of …

Pulmonary arterial hypertension (PAH) is caused by functional and structural changes in the
pulmonary vasculature, leading to increased pulmonary vascular resistance. The process of …

Pulmonary arterial hypertension (PAH) is a syndrome in which pulmonary arterial
obstruction increases pulmonary vascular resistance, which leads to right ventricular (RV) …

Recent investigations have suggested that it might be possible to reverse the pathology of
pulmonary arterial hypertension (PAH), a disorder that can be rapidly progressive and fatal …

Pulmonary arterial hypertension (PAH) is a lethal syndrome characterized by vascular
obstruction and right ventricular failure. Although the fundamental cause remains elusive …

Pulmonary arterial hypertension (PAH) is a complex disease that causes significant
morbidity and mortality and is clinically characterized by an increase in pulmonary vascular …

Rationale: Pulmonary arterial hypertension (PAH) is a lethal, female-predominant, vascular
disease. Pathologic changes in PA smooth muscle cells (PASMC) include excessive …

High-frequency echocardiography and high-field-strength magnetic resonance imaging
(MRI) are new noninvasive methods for quantifying pulmonary arterial hypertension (PAH) …

Idiopathic pulmonary arterial hypertension (PAH) is a life-threatening condition
characterized by pulmonary arteriolar remodeling. This investigation aimed to identify genes …

Pulmonary arterial hypertension (PAH) is a chronic disease characterized by a progressive
elevation in mean pulmonary arterial pressure. This occurs due to abnormal remodeling of …