All Stories

  1. Hospital discharge using salbutamol as required after acute attacks of wheeze in children: a service evaluation
  2. The tracheal system of the Common Wasp (Vespula vulgaris) – A micro-CT study
  3. Asthma, classical conditioning, and the autonomic nervous system – a hypothesis for why children wheeze
  4. Elexacaftor–Tezacaftor–Ivacaftor improves exercise capacity in adolescents with cystic fibrosis
  5. Structured transition is associated with improved outcomes in diabetes
  6. Projecting the impact of triple CFTR modulator therapy on intravenous antibiotic requirements in cystic fibrosis using patient registry data combined with treatment effects from randomised trials
  7. Meconium Ileus due to GUCY2C gene mutations in three unrelated South Indian families
  8. The impact of plasma 25‐hydroxyvitamin D on pulmonary function and exercise physiology in cystic fibrosis: A multicentre retrospective study
  9. Evaluation of the impact of shielding to avoid COVID-19 infection on respiratory symptoms in children with severe asthma
  10. Circulating biomarkers of antioxidant status and oxidative stress in people with cystic fibrosis: A systematic review and meta-analysis
  11. The implications of dysglycaemia on aerobic exercise and ventilatory function in cystic fibrosis
  12. A public health emergency among young people
  13. A rational approach to e-cigarettes: challenging ERS policy on tobacco harm reduction
  14. Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial
  15. Cephalosporin nitric oxide-donor prodrug DEA-C3D disperses biofilms formed by clinical cystic fibrosis isolates of Pseudomonas aeruginosa
  16. The journey of lumacaftor-ivacaftor from bench to bedside
  17. Reply to Askew and Green
  18. Determining the reasons for poorly controlled asthma in an adolescent
  19. Airway Microbiome and Development of Bronchopulmonary Dysplasia in Preterm Infants: A Systematic Review
  20. Psychometric evaluation of a patient-reported outcome measure in pancreatic exocrine insufficiency (PEI)
  21. Reply to Cooper
  22. Dysfunctional Breathing in Children and Adults With Asthma
  23. Cardiopulmonary exercise testing with supramaximal verification produces a safe and valid assessment of V̇o2max in people with cystic fibrosis: a retrospective analysis
  24. Evaluation of a regionally based preceptorship programme for newly qualified neonatal nurses
  25. Ready, Steady, Go – Achieving successful transition in cystic fibrosis
  26. The use of lumacaftor/ivacaftor to treat acute deterioration in paediatric cystic fibrosis
  27. Low-Dose Nitric Oxide as Targeted Anti-biofilm Adjunctive Therapy to Treat Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis
  28. Current and future therapies for Pseudomonas aeruginosa infection in patients with cystic fibrosis
  29. Contributions of Composition and Interactions to Bacterial Respiration Are Reliant on the Phylogenetic Similarity of the Measured Community
  30. Qualitative Assessment of the Symptoms and Impact of Pancreatic Exocrine Insufficiency (PEI) to Inform the Development of a Patient-Reported Outcome (PRO) Instrument
  31. Cephalosporin-3′-Diazeniumdiolate NO Donor Prodrug PYRRO-C3D Enhances Azithromycin Susceptibility of Nontypeable Haemophilus influenzae Biofilms
  32. Pseudomonas aeruginosainfection in cystic fibrosis: pathophysiological mechanisms and therapeutic approaches
  33. Cystic Fibrosis Nutrition – Chewing the Fat
  34. Nutritional outcomes in cystic fibrosis – are we doing enough?
  35. Routine use of daily oral vitamin K to treat infants with cystic fibrosis
  36. Ciprofloxacin during upper respiratory tract infections to reduce Pseudomonas aeruginosa infection in paediatric cystic fibrosis: a pilot study
  37. G385 RATNO - Reducing Antibiotic Tolerance using Nitric Oxide in Cystic Fibrosis: report of a proof of concept clinical trial
  38. Impact of antibiotic treatment for pulmonary exacerbations on bacterial diversity in cystic fibrosis
  39. Self-assessment
  40. Exhaled nitric oxide monitoring does not reduce exacerbation frequency or inhaled corticosteroid dose in paediatric asthma: a randomised controlled trial
  41. A Population-Based Study of Fish Allergy in the Philippines, Singapore and Thailand
  42. A Quantitative Analysis of Ureaplasma urealyticum and Ureaplasma parvum Compared with Host Immune Response in Preterm Neonates at Risk of Developing Bronchopulmonary Dysplasia
  43. Primary Tracheomalacia and Persistent Wheezing in Cystic Fibrosis During Infancy
  44. A 2-year post-authorization safety study of high-strength pancreatic enzyme replacement therapy (pancreatin 40,000) in cystic fibrosis
  45. Review article: enzyme supplementation in cystic fibrosis, chronic pancreatitis, pancreatic and periampullary cancer
  46. Manifesting carriage of a Duchenne muscular dystrophy mutation: an unusual cause of impaired lung function in CF
  47. Molecular Microbiological Characterization of Preterm Neonates at Risk of Bronchopulmonary Dysplasia
  48. The use of culture-independent tools to characterize bacteria in endo-tracheal aspirates from pre-term infants at risk of bronchopulmonary dysplasia
  49. Studying bacteria in respiratory specimens by using conventional and molecular microbiological approaches
  50. Colloidal silver for lung disease in cystic fibrosis
  51. Acute intestinal obstruction as a presentation of cystic fibrosis in infancy
  52. British Guideline on the Management of Asthma
  53. Cystic Fibrosis Diagnosed After 2 Months of Age Leads to Worse Outcomes and Requires More Therapy
  54. Idiopathic Bilateral Vocal Cord Palsy in Extremely Premature Neonates
  55. Chest x ray and high-resolution computed tomography in cystic fibrosis
  56. Use of 16S rRNA Gene Profiling by Terminal Restriction Fragment Length Polymorphism Analysis To Compare Bacterial Communities in Sputum and Mouthwash Samples from Patients with Cystic Fibrosis
  57. Juvenile Laryngeal Papillomatosis
  58. Resolution of peanut allergy following bone marrow transplantation for primary immunodeficiency
  59. The prevalence of stress urinary incontinence in patients with cystic fibrosis: an under-recognized problem
  60. Maldigestion and malabsorption of 13C labelled tripalmitin in gastrostomy-fed patients with cystic fibrosis
  61. A rare cause of upper airway obstruction in a 5-year-old girl: a laryngeal web
  62. Clinical application of direct sputum sensitivity testing in a severe infective exacerbation of cystic fibrosis
  63. Falsely elevated serum tobraycin levels in a patient receiving nebulised tobramycin
  64. Long term results of lung resection in cystic fibrosis patients with localised lung disease
  65. Bronchoalveolar lavage
  66. Somatizing disorders affecting the respiratory tract
  67. Editorial
  68. Diagnosis of cystic fibrosis : Indian perspective
  69. Faecal Elastase 1: A Marker of Exocrine Pancreatic Insufficiency in Cystic Fibrosis
  70. Pancreatic enzymes and fibrosing colonopathy
  71. A randomised controlled trial to assess the relative benefits of large volume spacers and nebulisers to treat acute asthma in hospital
  72. Colonic wall thickening is related to age and not dose of high strength pancreatin microspheres in children with cystic fibrosis
  73. Interferon alpha  treatment of molluscum contagiosum in immunodeficiency
  74. Diffuse Microcystic Pancreatic Enlargement in a Cystic Fibrosis Patient Causing Severe Gastrointestinal Symptoms and Successfully Treated by Total Pancreatectomy
  75. Inflammatory pseudotumor of the trachea in a ten-month-old infant
  76. Dietary fibre and the occurrence of gut symptoms in cystic fibrosis
  77. Use of a reformulated Oka strain varicella vaccine (SmithKline Beecham Biologicals/Oka) in healthy children
  78. Use of a reformulated Oka strain varicella vaccine (SmithKline Beecham Biologicals/Oka) in healthy children
  79. Flexible fibre-optic bronchoscopy in the management of lung complications in cystic fibrosis
  80. Lung resection in cystic fibrosis patients with localised pulmonary disease.
  81. Veno-venous haemodiafiltration in meningococcal septicaemia
  82. Bronchoscopic appearances of congenital lobar emphysema
  83. Effects of an acaricide on asthmatic children with house dust mite allergy
  84. Lung function reference values in Singaporean children aged 6-18 years.
  85. Day care and asthma morbidity
  86. Treating childhood asthma in Singapore: when West meets East
  87. Prednisolone and salbutamol in the hospital treatment of acute asthma.
  88. Use of budesonide in severe asthmatics aged 1-3 years.
  89. Audit strategies to reduce hospital admissions for acute asthma.
  90. Use of pulse oximetry in the hospital management of acute asthma in childhood
  91. Prolonged hypoxaemia after nebulised salbutamol.
  92. Prevention of viral induced asthma attacks using inhaled budesonide.
  93. Inhaled budesonide and behavioural disturbances
  94. Acute wheezy bronchitis--lumping and splitting.