All Stories

  1. The great leap backward: changes in the jumping performance of Australian children aged 11−12-years between 1985 and 2015
  2. Practical approach to the gastrointestinal manifestations of cystic fibrosis
  3. Bone mineral density is related to lung function outcomes in young people with cystic fibrosis-A retrospective study
  4. Quantitative assessment of airway dimensions in young children with cystic fibrosis lung disease using chest computed tomography
  5. The airway microbiota in early cystic fibrosis lung disease
  6. Socioeconomic Position Is Associated With Carotid Intima–Media Thickness in Mid‐Childhood: The Longitudinal Study of Australian Children
  7. Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?
  8. Asthma, bones and corticosteroids: Are inhaled corticosteroids associated with fractures in children with asthma?
  9. Vitamin D insufficiency in the first 6 months of infancy and challenge-proven IgE-mediated food allergy at 1 year of age: a case-cohort study
  10. Increasing airway obstruction from 8 to 18 years in extremely preterm/low-birthweight survivors born in the surfactant era
  11. Official American Thoracic Society Clinical Practice Guidelines: Diagnostic Evaluation of Infants with Recurrent or Persistent Wheezing
  12. Lack of transparency in software used to analyze multiple breath washout data
  13. The effects of maternal anxiety during pregnancy on IGF2/H19 methylation in cord blood
  14. Lung Clearance Index and Structural Lung Disease on Computed Tomography in Early Cystic Fibrosis
  15. Reply: Excess Risk of Cancer from Computed Tomography Scan Is Small but Not So Low as to Be Incalculable
  16. Multiple breath washout cannot be used for tidal breath parameter analysis in infants
  17. Impact of lung disease on respiratory impedance in young children with cystic fibrosis
  18. Progressive ventilation inhomogeneity in infants with cystic fibrosis after pulmonary infection
  19. Pulmonary Exacerbation Score in Cystic Fibrosis Patients: Reliability and Validity Testing
  20. Ability of the lung clearance index to detect inflammation and infection in preschool children with cystic fibrosis
  21. Infant and preschool lung function
  22. PRAGMA-CF. A Quantitative Structural Lung Disease Computed Tomography Outcome in Young Children with Cystic Fibrosis
  23. Matrix metalloproteinase activation by free neutrophil elastase contributes to bronchiectasis progression in early cystic fibrosis
  24. Cohort Profile: The Barwon Infant Study
  25. The ontogeny of naïve and regulatory CD4+ T-cell subsets during the first postnatal year: a cohort study
  26. Authors' response
  27. Use of neutrophil gelatinase-associated lipocalin (NGAL) in CF
  28. Lung clearance index during hospital admission in school-age children with cystic fibrosis
  29. Early Respiratory Infection Is Associated with Reduced Spirometry in Children with Cystic Fibrosis
  30. Antibiotic Management of Lung Infections in Cystic Fibrosis. II. Nontuberculous Mycobacteria, Anaerobic Bacteria, and Fungi
  31. Antibiotic Management of Lung Infections in Cystic Fibrosis. I. The Microbiome, Methicillin-Resistant Staphylococcus aureus , Gram-Negative Bacteria, and Multiple Infections
  32. Interpretation of lung function in infants and young children with cystic fibrosis
  33. Risk Factors for Bronchiectasis in Children With Cystic Fibrosis
  34. Chloral hydrate sedation for infant pulmonary function testing
  35. Induced sputum compared to bronchoalveolar lavage in young, non-expectorating cystic fibrosis children
  36. Increased rate of lung function decline in Australian adolescents with cystic fibrosis
  37. “Consensus statement for inert gas washout measurement using multiple- and single-breath tests.” Paul D. Robinson, Philipp Latzin, Sylvia Verbanck, Graham L. Hall, Alexander Horsley, Monika Gappa, Cindy Thamrin, Hubertus G.M. Arets, Paul Aurora, Susann...
  38. Staphylococcus aureus in early cystic fibrosis lung disease
  39. Risk Factors for Bronchiectasis in Children with Cystic Fibrosis
  40. Progression of structural lung disease on CT scans in children with cystic fibrosis related diabetes
  41. Geographical Differences in First Acquisition of Pseudomonas aeruginosa in Cystic Fibrosis
  42. An Official American Thoracic Society Workshop Report: Optimal Lung Function Tests for Monitoring Cystic Fibrosis, Bronchopulmonary Dysplasia, and Recurrent Wheezing in Children Less Than 6 Years of Age
  43. Early intervention studies in infants and preschool children with cystic fibrosis: are we ready?
  44. Consensus statement for inert gas washout measurement using multiple- and single- breath tests
  45. Authors’ response
  46. Glucose Tolerance during Pulmonary Exacerbations in Children with Cystic Fibrosis
  47. Molecular Epidemiology Of Staphylococcus Aureus Infections In A Paediatric Treatment Centre
  48. Small macrophages are present in early childhood respiratory disease
  49. The Influence Of Sighing Respirations On Infant Lung Function Measured Using Multiple Breath Washout Gas Mixing Techniques
  50. Geographical Differences In Acquisition Of Pseudomonas Aeruginosa
  51. Progression of early structural lung disease in young children with cystic fibrosis assessed using CT
  52. Pleural fluid nucleic acid testing enhances pneumococcal surveillance in children
  53. Spontaneous chylothorax in a 2-year-old child
  54. Bacterial Causes of Empyema in Children, Australia, 2007–2009
  55. Monitoring of Structure and Function in Early Cystic Fibrosis Lung Disease
  56. Air Trapping on Chest CT Is Associated with Worse Ventilation Distribution in Infants with Cystic Fibrosis Diagnosed following Newborn Screening
  57. Infection, Inflammation, and Lung Function Decline in Infants with Cystic Fibrosis
  58. A bedside assay to detect streptococcus pneumoniae in children with empyema
  59. Lung function in preschool children with a history of wheezing measured by forced oscillation and plethysmographic specific airway resistance
  60. Lung function in children with repaired tracheo-oesophageal fistula using the forced oscillation technique
  61. Progression Of Structural Lung Disease On CT Scans In Children With Cystic Fibrosis Related Diabetes
  62. Early Pulmonary Inflammation Is Associated With Worse Nutritional Status In Infants And Young Children With CF Diagnosed By Newborn Screening
  63. Identification of The Bacterial Causes of Childhood Empyema in Australia by Enhanced Molecular Surveillance
  64. Early bronchiectasis in cystic fibrosis detected by surveillance CT
  65. Bronchiectasis in Infants and Preschool Children Diagnosed with Cystic Fibrosis after Newborn Screening
  66. Evidence-based management of paediatric primary spontaneous pneumothorax
  67. Lung Disease at Diagnosis in Infants with Cystic Fibrosis Detected by Newborn Screening
  68. Endobronchial ultrasound in pediatric pulmonology
  69. Paralysis and a perihilar protuberance: An unusual presentation of sarcoidosis in a child
  70. Pneumonia and Other Respiratory Infections
  71. Respiratory function during infancy in survivors of the INNOVO trial
  72. Vitamin D in infants with cystic fibrosis diagnosed by newborn screening
  73. Lung Function in Infants with Cystic Fibrosis Diagnosed by Newborn Screening
  74. Safety of bronchoalveolar lavage in young children with cystic fibrosis
  75. Role of high-resolution computed tomography in the detection of early cystic fibrosis lung disease
  76. Early Detection of Lung Disease in Children with Cystic Fibrosis Using Lung Function
  77. A Three-Way Comparison of Tuberculin Skin Testing, QuantiFERON-TB Gold and T-SPOT.TB in Children
  78. Lung Function from Infancy to the Preschool Years after Clinical Diagnosis of Cystic Fibrosis
  79. Airway function in infants treated with inhaled nitric oxide for persistent pulmonary hypertension
  80. Optimizing Medications for Poorly Controlled Asthma
  81. Interferon-gamma release assays in children – No better than tuberculin skin testing?
  82. The Timing of rhDNase in relation to airway clearance therapy-unplugged
  83. Clinical scoring systems in cystic fibrosis
  84. Diameter of paediatric sized flexible bronchoscopes: When size matters
  85. Ventilation Inhomogeneities in Patients with Cystic Fibrosis
  86. Recent Advances in Infant and Pre-School Lung Function
  87. Intussusceptions arising from two different sites in a child with cystic fibrosis
  88. The Evolution of Airway Function in Early Childhood Following Clinical Diagnosis of Cystic Fibrosis
  89. Relative Ability of Full and Partial Forced Expiratory Maneuvers to Identify Diminished Airway Function in Infants with Cystic Fibrosis
  90. Lung function testing in infants with cystic fibrosis: Lessons from the past and future directions
  91. Respiratory Conditions
  92. Physiologic Assessment of Lung Growth and Development Throughout Infancy and Childhood