The paranasal sinuses can be a focus for colonisation of the cystic fibrosis (CF) lungs with
pathogens. In the sinuses, bacteria can adapt to the lung environment and enhance their …

Conclusions: Chronic rhinosinusitis diagnosed according to the European Position Paper on
Rhinosinusitis and Nasal Polyps 2012, not by computed tomography alone, is one of the …

The cystic fibrosis (CF) respiratory tract is inhabited by complex polymicrobial communities
[1–4]. The sinonasal site has been proposed as a gateway and reservoir for subsequent …

More research is needed to discriminate offending pathogens from contaminating microbiota
and to be able to identify the anatomical origin of the many detected microbes. Furthermore …

Background Tracheal diverticula (TD) are rare anomalies that may harbor infected
secretions, posing potential risk to patients with lung disease. In an end-stage cystic fibrosis …

People with the genetic disorder cystic fibrosis (CF) harbor lifelong respiratory infections,
with morbidity and mortality frequently linked to chronic lung infections dominated by the …

Муковисцидоз (МВ)—системное наследственное заболевание, характеризующееся
тяжелыми нарушениями функций желудочно-кишечного тракта и органов дыхания …

Муковисцидоз (МВ)-системное наследственное заболевание, характеризующееся
тяжелыми нарушениями функций желудочно-кишечного тракта и органов дыхания …

The respiratory tract is known to harbor a microbial community including bacteria, viruses,
and fungi. New techniques contribute enormously to the identification of unknown or culture …

Cystic Fibrosis is an autosomal recessive genetic disease that manifests in multiple organs
leading to various complications throughout the patient, but most notable is the progressive …