Introduction Primary ciliary dyskinesia (PCD) is characterized by an alteration in the ciliary
structure causing difficulty in the clearance of respiratory secretions. Diagnosis is complex …

Background: Due to the lack of a gold standard diagnostic test, reference centres with
experienced personnel and costly procedures are needed for primary ciliary dyskinesia …

Air-liquid interface (ALI) cell culture of primary airway progenitors enables the differentiation
and recapitulation of a pseudostratified epithelium in vitro, providing a highly useful tool for …

Background: Primary Ciliary Dyskinesia (PCD) represents a rare condition marked by an
abnormal mobility pattern of cilia and flagella, resulting in impaired mucociliary clearance …

4. Chang RYK, Chen K, Wang J, Wallin M, Britton W, Morales S, et al. Proof-of-principle
study in a murine lung infection model of antipseudomonal activity of phage PEV20 in a dry …

Primary Ciliary Dyskinesia (PCD) is a genetic motile ciliopathy, leading to significant
otosinopulmonary disease. PCD diagnosis is often missed or delayed due to challenges …

Ciliary dyskinesia in severe asthma is not affected by chronic mucus hypersecretion | European
Respiratory Society Skip to main content Main menu Home Current issue Early View Archive …

Abstract Background Primary Ciliary Dyskinesia (PCD) diagnosis relies on a combination of
tests which may include (a) nasal Nitric Oxide (nNO),(b) High Speed Video Microscopy …

Rationale: Primary ciliary dyskinesia is a rare genetic disease affecting ciliary motility and
causing respiratory symptoms. Diagnosis can be done by high-speed-videomicroscopy …

Background Primary ciliary dyskinesia (PCD) is diagnosed through multiple methods,
including transmission electron microscopy (TEM), a high-speed video microscopy analysis …