Pulmonary hypertension (PH) encompasses a syndrome of diseases that are characterized
by elevated pulmonary artery pressure and pulmonary vascular remodeling and that …

Pulmonary arterial hypertension (PAH) is a disease resulting in increased right ventricular
(RV) afterload and RV remodeling. PAH results in altered RV structure and function at …

Pulmonary arterial hypertension (PAH) is a rare, life-threatening condition characterized by
dysregulated metabolism, pulmonary vascular remodeling, and loss of pulmonary vascular …

With each heartbeat, the right ventricle (RV) inputs blood into the pulmonary vascular (PV)
compartment, which conducts blood through the lungs at low pressure and concurrently fills …

17b-estradiol (E2), the most abundant female sex steroid, has been implicated in the
development and progression of pulmonary arterial hypertension (PAH)(1, 2). Although …

Left heart failure (LHF) is the most common cause of pulmonary hypertension, which confers
an increase in morbidity and mortality in this context. Pulmonary vascular resistance has …

Nitric oxide (NO) inhalation improves pulmonary hemodynamics in participants with
pulmonary arterial hypertension (PAH). Although it can reduce pulmonary vascular …

Pregnancy with pulmonary hypertension (PH) seriously threatens the life and safety of
mothers and infants. Here, the long-term effect of maternal PH on the postpartum growth of …

Background Wave reflection is enhanced in patients with pulmonary arterial hypertension
(PAH), which may be derived from a mismatch of pulmonary artery (PA) impedance between …

Background: Prior studies have established the impact of sex differences on pulmonary
arterial hypertension (PAH). However, it remains unclear whether these sex differences …