The lungs of patients with cystic fibrosis harbor a different microbial makeup, including less diversity of species, than the lungs of healthy individuals, according to a study published Wednesday ...

Between the first week of pulmonary rehabilitation and the last recorded session before transplantation, lung transplant ...

The Program for Pulmonary Fibrosis and Interstitial Lung Disease's mission is to provide state of the art evaluation and treatment for patients with interstitial lung diseases (ILD). The University of ...

Cystic fibrosis is an inherited genetic disease that causes a build-up of mucus in the lungs and digestive system. It causes ...

In a recent study published in the Journal of Cystic Fibrosis, Don Ingber and his group at the Wyss ... In 2010, his team created the first lung-on-a-chip, a small in vitro model that recreates the ...

Cystic fibrosis is a life-threatening genetic disease that clogs the lungs with thick, sticky mucus, leading to chronic infections and severe organ damage. Despite breakthrough medications that have ...

Learn how to navigate cystic fibrosis care with confidence, from treatments and school plans to building a supportive medical ...

All states should adopt updated screening protocols so more newborns with cystic fibrosis can be diagnosed in the first weeks of life, when interventions can have the greatest benefit, according to ...

Researchers at The University of Manchester in collaboration with Manchester University NHS Foundation Trust (MFT) are launching a new Cystic Fibrosis Innovation Hub to accelerate the development of ...

The Program for Pulmonary Fibrosis and Interstitial Lung Disease's mission is to provide state of the art evaluation and treatment for patients with interstitial lung diseases (ILD). The University of ...