Pulmonary arterial hypertension (PAH) is a rare disease characterized by pulmonary
vascular remodeling leading to right heart failure and death. To date, despite the three …

Pulmonary arterial hypertension (PAH) is a progressive disease characterized by elevated
pulmonary arterial pressure due to increased pulmonary vascular resistance, secondary to …

Pulmonary arterial hypertension (PAH) is an orphan disease of the cardiopulmonary unit
that reflects an obstructive pulmonary vasculopathy and presents with hypertrophy …

Pulmonary arterial hypertension (PAH) is a vascular remodeling disease of the lungs
resulting in heart failure and premature death. Although, until recently, it was thought that …

Numerous molecular abnormalities have been described in pulmonary arterial hypertension
(PAH), complicating the translation of candidate therapies to patients because, typically, 1 …

Pulmonary arterial hypertension (PAH) is characterized by impaired regulation of pulmonary
hemodynamics and vascular growth. Alterations of metabolism and bioenergetics are …

Pulmonary hypertension (PH) is a deadly and increasingly prevalent vascular disease
characterized by excessive pulmonary vascular remodeling and right ventricular dysfunction …

Significance: Pulmonary hypertension (PH) is a progressive disease characterized by
pulmonary vascular remodeling and lung vasculopathy. The disease displays progressive …

Pulmonary arterial hypertension (PAH) is a syndrome characterised by an increase in
pulmonary vascular resistance. This results in elevated resting pulmonary artery pressure …

Pulmonary hypertension (PH) represents a group of disorders characterized by elevated
mean pulmonary artery (PA) pressure, progressive right ventricular failure, and often death …