The receptor for advanced glycation endproducts (RAGE) is a pro-inflammatory pattern
recognition receptor (PRR) that has been implicated in the pathogenesis of numerous …

Interstitial lung disease in children (chILD) is rare, and most centres will only see a few
cases/year. There are numerous possible underlying diagnoses, with specific and non …

Objective Systemic juvenile idiopathic arthritis (JIA) is associated with a recently recognized,
albeit poorly defined and characterized, lung disease (LD). The objective of this study was to …

Methods A working group from PPHNet specialists that included neonatologists,
cardiologists, pulmonologists, and intensivists was established to create this document …

Genetic predisposition to pulmonary fibrosis has been confirmed by the discovery of several
gene mutations that cause pulmonary fibrosis. Although genetic sequencing of familial …

The National Heart, Lung, and Blood Institute is funding an effort to create a molecular atlas
of the developing lung (LungMAP) to serve as a research resource and public education …

Interstitial lung diseases (ILD) or diffuse parenchymal lung diseases (DPLD) comprise a
large number of disorders. Disease definition and classification allow advanced and …

Club cell secretory protein (CC16) is encoded by the SCGB1A1 gene. It is also known as
CC10, secretoglobin, or uteroglobin. CC16 is a 16 kDa homodimeric protein secreted …

Advances in physiology and biochemistry have provided fundamental insights into the role
of pulmonary surfactant in the pathogenesis and treatment of preterm infants with respiratory …

Childhood interstitial lung diseases (chILDs) are rare and heterogeneous diseases with
significant morbidity and mortality. An accurate and quick aetiological diagnosis may …