Background The contribution of registered nurses towards safe patient care has been
demonstrated in many studies. However, most of the evidence linking staffing levels to outcomes is …

Background Primary ciliary dyskinesia (PCD) is a heterogeneous inherited disorder caused
by mutations in approximately 50 cilia-related genes. PCD genotype–phenotype …

Background Diagnosis of primary ciliary dyskinesia (PCD) relies on a combination of tests.
High-speed video microscopy analysis (HSVA) is widely used to contribute to the diagnosis. It …

Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sino-pulmonary
disease, with symptoms starting soon after birth. A European Respiratory …

Objectives Health systems worldwide are faced with the challenge of adequately staffing their
hospital services. Much of the current research and subsequent policy has been focusing …

Electronic health records (EHRs) offer the opportunity to ascertain clinical outcomes at large
scale and low cost, thus facilitating cohort studies, quality of care research and clinical trials. …

Rationale Primary ciliary dyskinesia is a genetically heterogeneous inherited condition
characterised by progressive lung disease arising from abnormal cilia function. Approximately …

Primary ciliary dyskinesia (PCD) is a rare genetic disease that affects the motility of cilia,
leading to impaired mucociliary clearance. It is estimated that the vast majority of patients with …

Bacterial pathogens need to acquire nutrients from the host, but for many nutrients their
importance during infection remain poorly understood. We have investigated the importance of …

Primary ciliary dyskinesia (PCD) is associated with abnormal organ positioning (situs) and
congenital heart disease (CHD). This study investigated genotype–phenotype associations in …