Reports and Findings
Protease elastase exocytosis by airway neutrophils occurs in all cystic fibrosis children, and its cellular measure correlates with early lung damage
This Research Note has explored the strengths, risks and potential complexity of adaptive trials
Structural changes identified on CT scans in primary ciliary dyskinesia are not identical to those previously described in cystic fibrosis patients
Our maps provide a baseline for measuring change and a mechanism to guide interventions during the era of the Sustainable Development Goals
Results indicate that early childhood education is beneficial for children's early development
The findings indicated that in spite of continued promotion of the AIFG over the past ten years achieving the around six months guideline is challenging
This review will discuss the necessary steps required for a Bayesian adaptive platform trial to optimize treatment of pulmonary exacerbations of cystic fibrosis
We confirmed the strong association between high DAT and/or rK39 titers and progression to disease among asymptomatic subjects
First study to show that the increase in extreme preterm birth in high-income jurisdiction is no longer evident after medical terminations and birth defects are excluded
Streptococcus pneumoniae causes substantial morbidity and mortality among children. The introduction of pneumococcal conjugate vaccines (PCV) has the potential to dramatically reduce disease burden. As with any vaccine, it is important to evaluate PCV impact, to help guide decision-making and resource-allocation.