Rationale: Cystic fibrosis (CF) is an autosomal recessive disease characterized by abnormal
airways secretions, chronic endobronchial infection, and progressive airway obstruction …

Pulmonary exacerbations have very important consequences in cystic fibrosis (CF), both in
terms of current morbidity as well as implications for long term morbidity and mortality. Even …

Background Bronchiectasis develops early in the course of cystic fibrosis, being detectable
in infants as young as 10 weeks of age, and is persistent and progressive. We sought to …

Background Studies suggest that a diet rich in omega‐3 essential fatty acids may have
beneficial anti‐inflammatory effects for chronic conditions such as cystic fibrosis. Objectives …

Cystic fibrosis (CF) lung disease is characterized by chronic bacterial infection and an
unremitting inflammatory response, which are responsible for most of CF morbidity and …

Non-cystic fibrosis bronchiectasis remains a common and important respiratory disease to
date. It is a chronic pathology and consequently the patients usually require continuous …

Abstract In Cystic Fibrosis (CF), mutations of the CFTR gene result in defective Cl− secretion
and Na+ hyperabsorption by epithelia which leads to airway lumen dehydration and mucus …

В статье приводятся данные по фармакокинетике нестероидного
противовоспалительного средства (НПВС) ибупрофена, представлен обзор …

There is increasing evidence to suggest the presence of chronic inflammation in the
gastrointestinal (GI) tract of cystic fibrosis (CF) patients. Some CF patients continue to have …

The paper presents data on the pharmacokinetics of the nonsteroidal anti-inflammatory drug
ibuprofen and a review of the evidence base that suggests its clinical efficacy and safety in …