Pulmonary arterial hypertension (PAH) is a relatively rare but potentially life-threatening
disease. In most forms, the disease is likely to be diagnosed late and is associated with …

Abstract Fraidenburg, Dustin, Jason Yuan. Current and future targets for pulmonary arterial
hypertension. High Alt Med Biol 14: 134–143, 2013.—Pulmonary arterial hypertension …

Pulmonary arterial hypertension (PAH) is a rare condition that has attracted much attention
in recent years. Previously perceived as an orphan within pulmonary pathologies due to its …

Pulmonary arterial hypertension (PAH) is a disease characterized by progressive loss and
remodeling of the pulmonary arteries, resulting in right heart failure and death. Until recently …

Although idiopathic pulmonary arterial hypertension, formerly called “primary,” is rare, other
forms of PAH and associated cor pulmonale are more prevalent than conventionally …

Pulmonary arterial hypertension (PAH) is a rare disease affecting mainly the pre-capillary
pulmonary vascular bed. However, some forms of the disease have venous/capillary …

Pulmonary arterial hypertension (PAH) is a disease of progressive pulmonary vascular
remodeling due to abnormal proliferation of pulmonary vascular endothelial and smooth …

Pulmonary arterial hypertension (PAH) is a pathological condition of the small pulmonary
arteries. PAH is characterized histopathologically by vasoconstriction, vascular proliferation …

Pulmonary Arterial Hypertension (PAH) is a clinical syndrome consisting of physiologic/
hemodynamic criteria that are a consequence of several etiologies. Confirmation of …