Association between Rheumatoid Arthritis and Pulmonary Hypertension: Data from the French Pulmonary Hypertension Registry

In patients with PH due to res- piratory disease, the percentages of responders ac- cording to the treating physician seemed larger, whereas the percentage of acute responder

The objective of this study is to investigate the ability and accuracy of OCT to detect and quantify intimal fibrosis, as a marker of histological remodeling of the pulmonary

During the vascular remodeling process in PAH subjects, Ang-1 was significantly decreased in the pulmonary arteries along with a reduction of Tie-2, a novel

Paediatric patients from age 0–18 years with the di- agnosis of pulmonary arterial hypertension of all aetiolo- gies except persistent pulmonary hypertension of the newborn

Rapamycin given in vivo to rats therefore inhibited the mTOR signaling pathway in a manner very similar to that seen with direct cell exposure, inhibiting both mTORC1

has received payment for lectures from Actelion. has received payment for consultancy and lectures from Actelion, Bayer, BMS, GlaxoSmithKline, MSD, and Pfizer. His institution

Thiene et al demonstrated that lung segments perfused by large, nonstenotic systemic collateral arteries in patients with pulmonary atresia had features of proliferative

Pulmonary hypertension is defined as an invasive pul- monary artery mean pressure (mPAP) ≥25 mm Hg ob- tained during right heart catheterisation at rest [16]1. A resting mPAP between