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 …

The diagnosis and management of infants and children with a significant viral lower
respiratory tract illness remains the subject of much debate and little progress. Over the …

Objective To describe the prevalence of pulmonary arterial hypertension (PAH)-associated
gene mutations, and other genetic characteristics in a national cohort of children with PAH …

Background Bleomycin (BLM) is a chemotherapy drug used to treat cancer, one of which
side effects is that it can lead to pulmonary fibrosis (PF). Atractylenoide III (AtrIII), derived …

Introduction Interstitial lung diseases (ILDs) can be caused by mutations in the SFTPA1 and
SFTPA2 genes, which encode the surfactant protein (SP) complex SP-A. Only 11 SFTPA1 or …

Vaping-associated pulmonary injury (VAPI) is a severe respiratory disorder associated with
the inhalation of nicotine, tetrahydrocannabinol, cannabidiol, or other active substances …

Interstitial lung disease (ILD) in children (chILD) is a heterogeneous group of rare respiratory
disorders that are mostly chronic and associated with high morbidity and mortality. The …

The term children interstitial lung diseases (chILD) refers to a heterogeneous group of rare
diseases that diffusely affect the lung. ChILD specific to children younger than 2 years of age …

Chronic lung disease accounts for a significant global burden with respect to death,
disability, and health-care costs. Due to the heterogeneous nature and limited treatment …

The clinical phenotype of a TBX4 variant has recently been recognised to expand from bone
disorders to different types of lung diseases. Recent data suggest that variants of TBX4, a …