All Stories

  1. Pulmonary Exacerbations and Treatment in PCD: A Narrative Review
  2. Tracking early cystic fibrosis in the new era
  3. The CARMUCI Study Design: A Double‐Blind, Cross‐Over Sham‐Controlled Trial of Indoor Air Purification in People With Cystic Fibrosis and Primary Ciliary Dyskinesia
  4. Quantifying the effects of mucociliary clearance and cilia–drug interactions on partial drug dissolution and epithelial deposition in the airway surface liquid
  5. Pulmonary exacerbations in patients with genetically confirmed PCD: A prospective observational multicentre study
  6. Cystic Fibrosis and Primary Ciliary Dyskinesia Share Extensive Similarities: Is It Time to Place Them Under a Common Umbrella?
  7. Multiple breath washout in primary ciliary dyskinesia: a systematic review of the literature
  8. A BEAT-PCD consensus statement: a core outcome set for pulmonary disease interventions in primary ciliary dyskinesia
  9. MEDEA randomised intervention study protocol in Cyprus, Greece and Israel for mitigation of desert dust health effects in adults with atrial fibrillation
  10. Observational study of health utilities in adult primary ciliary dyskinesia patients: preliminary data on associations with molecular diagnosis, clinical phenotype and HRQOL measures
  11. “Normative data for multiple breath washout outcomes in school-aged Caucasian children.” Pinelopi Anagnostopoulou, Philipp Latzin, Renee Jensen, et al. Eur Respir J 2020; 55: 1901302.
  12. Normative multiple-breath washout data in school-aged children corrected for sensor error
  13. The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTN
  14. Pediatric asthma symptom control during lockdown for the COVID‐19 pandemic in Spring 2020: A prospective community‐based study in Cyprus and Greece
  15. Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry
  16. Neonatal ßENaC-Tg mice with cystic fibrosis-like lung disease possess enlarged airspaces
  17. Prospective assessment of pediatric asthma morbidity in Cyprus and Greece during COVID-19 lockdown measures in Spring 2020
  18. Compliance of asthmatic children to lockdown measures for the COVID-19 pandemic: Objective assessment using wearable sensors
  19. Implementation of multigene panel NGS diagnosis in the national primary ciliary dyskinesia cohort of Cyprus: An island with a high disease prevalence
  20. Use of wearable sensors to assess compliance of asthmatic children in response to lockdown measures for the COVID-19 epidemic
  21. Health state utilities in adult Primary Ciliary Dyskinesia patients
  22. Dehydration and electrolyte imbalance: a common presenting manifestation of cystic fibrosis in Cyprus
  23. Evaluation of a multiple breath nitrogen washout system in children
  24. Normative data for multiple breath washout outcomes in school-aged Caucasian children
  25. A mathematical model to understand the airway clearance in cystic fibrosis
  26. A multi-scale model of gas transport in the lung to study heterogeneous lung ventilation during the multiple-breath washout test
  27. An innovative lung model for multiple breath washout testing in health and disease
  28. A Multi-Scale Lung Model to Study Heterogeneous Ventilation During the Multiple-Breath Washout Test
  29. Exposure to moderate air pollution and associations with lung function at school-age: A birth cohort study
  30. Variability of Tidal Breathing Parameters in Preterm Infants and Associations with Respiratory Morbidity during Infancy: A Cohort Study
  31. Respiratory rate in infants with cystic fibrosis throughout the first year of life and association with lung clearance index measured shortly after birth
  32. Dynamics of respiratory symptoms during infancy and associations with wheezing at school age
  33. Normative data for the new setup of the SF6 multiple-breath washout in unsedated infants
  34. Protective effects of breastfeeding on respiratory symptoms in infants with 17q21 asthma risk variants
  35. A modified CO2/O2 Guedel airway improves capnographic accuracy compared with a CO2/O2 nasal cannula
  36. Comparison of different analysis algorithms to calculate multiple-breath washout outcomes
  37. Efficacy and safety of the combination fluticasone propionate plus salmeterol in asthmatic preschoolers: An observational study
  38. Infant multiple breath washout using a new commercially available device: Ready to replace the previous setup?
  39. Elevated lung clearance index in infants with cystic fibrosis shortly after birth
  40. Multiple breath washout outcomes in infants are setup-dependent
  41. Temporal behavior of respiratory symptoms during infancy and associations with asthma at school age
  42. Interrupter technique in infancy: Higher airway resistance and lower short‐term variability in preterm versus term infants
  43. Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls
  44. Unexpected results in infant multiple breath washout: Is the truth hidden in the washin?
  45. Applicability of interrupter technique to assess airways resistance in term and preterm infants
  46. Efficacy and safety of inhaled corticosteroids in combination with a long-acting beta2-agonist in asthmatic children under age 5
  47. Usefulness of exhaled nitric oxide in newborns to predict asthma at school age
  48. New reference values for N2multiple breath washout outcomes in pre-school and school-aged children
  49. Predictive value of exhaled nitric oxide in healthy infants for asthma at school age
  50. Lung clearance index and moment ratios at different cut-off values in infant multiple-breath washout measurements
  51. Multiple breath washout analysis in infants: quality assessment and recommendations for improvement
  52. Underestimation of lung clearance index values in infants with cystic fibrosis due to software analysis algorithms
  53. False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms
  54. SLC26A9-mediated chloride secretion prevents mucus obstruction in airway inflammation
  55. mCLCA3 Does Not Contribute to Calcium-Activated Chloride Conductance in Murine Airways
  56. : Figure 2–
  57. Allergic airway inflammation induces a pro-secretory epithelial ion transport phenotype in mice