All Stories

  1. Revised ISHAM-ABPA working group clinical practice guidelines for diagnosing, classifying and treating allergic bronchopulmonary aspergillosis/mycoses
  2. Food and Drug Administration (FDA) Public Workshop Summary—Addressing Challenges in Inhaled Antifungal Drug Development
  3. Correction: Moss, R.B. Severe Fungal Asthma: A Role for Biologics and Inhaled Antifungals. J. Fungi 2023, 9, 85
  4. Evaluation of Acebilustat, a Selective Inhibitor of Leukotriene B4 Biosynthesis, for Treatment of Outpatients With Mild-Moderate Coronavirus Disease 2019: A Randomized, Double-Blind, Placebo-Controlled Phase 2 Trial
  5. Severe Fungal Asthma: A Role for Biologics and Inhaled Antifungals
  6. Rate of Lung Function Decline in People with Cystic Fibrosis Having a Residual Function Gene Mutation
  7. Clinician variability in the diagnosis and treatment of aspergillus fumigatus-related conditions in cystic fibrosis: An international survey
  8. Biomarkers for the Diagnosis of Allergic Bronchopulmonary Aspergillosis in Cystic Fibrosis: A Systematic Review and Meta-Analysis
  9. Diagnosing allergic bronchopulmonary aspergillosis/mycosis: Return to lost horizons
  10. Mucosal humoral immunity in cystic fibrosis - a tangled web of failed proteostasis, infection and adaptive immunity
  11. Long-Term Ivacaftor in People Aged 6 Years and Older with Cystic Fibrosis with Ivacaftor-Responsive Mutations
  12. Manifestations of pulmonary aspergillosis in pediatrics
  13. Early Aspergillosis in Cystic Fibrosis and Air Trapping: Guilt by Association?
  14. Mucus plugging, air trapping, and bronchiectasis are important outcome measures in assessing progressive childhood cystic fibrosis lung disease
  15. Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function
  16. Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adults
  17. The myriad challenges of respiratory fungal infection in cystic fibrosis
  18. Cystic fibrosis transmembrane conductance regulator modulators: precision medicine in cystic fibrosis
  19. Susceptibility of Candida albicans from Cystic Fibrosis Patients
  20. The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurements
  21. Assessment of safety and efficacy of long-term treatment with combination lumacaftor and ivacaftor therapy in patients with cystic fibrosis homozygous for the F508del-CFTR mutation (PROGRESS): a phase 3, extension study
  22. Are Cystic Fibrosis Aspergillus fumigatus Isolates Different? Intermicrobial Interactions with Pseudomonas
  23. Basophil activation test determination of CD63 combined with CD203c is not superior to CD203c alone in identifying allergic bronchopulmonary aspergillosis in cystic fibrosis
  24. Allergic Bronchopulmonary Aspergillosis
  25. “Blood basophil activation is a reliable biomarker of allergic bronchopulmonary aspergillosis in cystic fibrosis.” Yael Gernez, Jeffrey Waters, Bojana Mirković, Gillian M. Lavelle, Colleen E. Dunn, Zoe A. Davies, Cassie Everson, Rabindra Tirouvanziam, ...
  26. Effect of Media Modified To Mimic Cystic Fibrosis Sputum on the Susceptibility of Aspergillus fumigatus, and the Frequency of Resistance at One Center
  27. Earth Mover’s Distance (EMD): A True Metric for Comparing Biomarker Expression Levels in Cell Populations
  28. Modulatory Effects of Aspergillus Colonization and Abpa on Blood and Sputum Granulocytes in CF
  29. The basophil surface marker CD203c identifies Aspergillus species sensitization in patients with cystic fibrosis
  30. Discusses advances in treating a common and serious complication of allergic asthma.
  31. Blood basophil activation is a reliable biomarker of allergic bronchopulmonary aspergillosis in cystic fibrosis
  32. Inhibition of Aspergillus fumigatus and Its Biofilm by Pseudomonas aeruginosa Is Dependent on the Source, Phenotype and Growth Conditions of the Bacterium
  33. Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508delCFTR
  34. Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trial
  35. Molecular epidemiology of Aspergillus collected from cystic fibrosis patients
  36. Recent advances in cystic fibrosis
  37. Fungi in Cystic Fibrosis and Non–Cystic Fibrosis Bronchiectasis
  38. Long-term treatment with oral N-acetylcysteine: Affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial
  39. A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial
  40. Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial
  41. A Little CFTR Goes a Long Way: CFTR-Dependent Sweat Secretion from G551D and R117H-5T Cystic Fibrosis Subjects Taking Ivacaftor
  42. Basophil Activation Is a Reliable Biomarker Of Allergic Bronchopulmonary Aspergillosis (ABPA) In CF: One Year Results Of a Longitudinal Cohort Study
  43. Treatment options in severe fungal asthma and allergic bronchopulmonary aspergillosis
  44. Allergic bronchopulmonary aspergillosis: review of literature and proposal of new diagnostic and classification criteria
  45. Optimizing Nasal Potential Difference Analysis for CFTR Modulator Development: Assessment of Ivacaftor in CF Subjects with the G551D-CFTR Mutation
  46. Safety and early treatment effects of the CXCR2 antagonist SB-656933 in patients with cystic fibrosis
  47. Pitfalls of Drug Development: Lessons Learned from Trials of Denufosol in Cystic Fibrosis
  48. Sputum Tobramycin Concentrations in Cystic Fibrosis Patients with Repeated Administration of Inhaled Tobramycin
  49. Current treatment options for invasive aspergillosis
  50. Blood basophils from cystic fibrosis patients with allergic bronchopulmonary aspergillosis are primed and hyper-responsive to stimulation by aspergillus allergens
  51. Long term effects of denufosol tetrasodium in patients with cystic fibrosis
  52. Fungi and allergic lower respiratory tract diseases
  53. Specific Induction Of CD203c Expression In Blood Basophils Discriminates Between CF patients With Aspergillus Colonization And Those With CF-ABPA
  54. Socioeconomic Status and the Likelihood of Antibiotic Treatment for Signs and Symptoms of Pulmonary Exacerbation in Children with Cystic Fibrosis
  55. Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for theF508del-CFTRmutation
  56. Denufosol Tetrasodium in Patients with Cystic Fibrosis and Normal to Mildly Impaired Lung Function
  57. Allergic bronchopulmonary aspergillosis and Aspergillus infection in cystic fibrosis
  58. Baseline Characteristics and Factors Associated With Nutritional and Pulmonary Status at Enrollment in the Cystic Fibrosis EPIC Observational Cohort
  59. Safety, Tolerability, and Efficacy of High-Frequency Chest Wall Oscillation in Pediatric Patients With Cerebral Palsy and Neuromuscular Diseases: An Exploratory Randomized Controlled Trial
  60. Cystic fibrosis HRCT scores correlate strongly with pseudomonas infection
  61. Study Of Sublingual Immunotherapy In Subjects With Dermatophagoides Farniae And Timothy Grass Allergy
  62. Highlights of a workshop to discuss targeting inflammation in cystic fibrosis
  63. No Detectable Improvements in Cystic Fibrosis Transmembrane Conductance Regulator by Nasal Aminoglycosides in Patients with Cystic Fibrosis with Stop Mutations
  64. Duration of treatment effect after tobramycin solution for inhalation in young children with cystic fibrosis
  65. Critique of trials in allergic bronchopulmonary aspergillosis and fungal allergy
  66. High-dose oral N -acetylcysteine, a glutathione prodrug, modulates inflammation in cystic fibrosis
  67. Pathophysiology and immunology of allergic bronchopulmonary aspergillosis
  68. Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis
  69. Quantitative air‐trapping analysis in children with mild cystic fibrosis lung disease
  70. Composite Spirometric–Computed Tomography Outcome Measure in Early Cystic Fibrosis Lung Disease
  71. Significant Microbiological Effect of Inhaled Tobramycin in Young Children with Cystic Fibrosis
  72. Allergic Bronchopulmonary Aspergillosis
  73. Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein
  74. Spirometer-Triggered High Resolution Computed Tomography (HRCT) of the Chest, Clinical Score, and Pulmonary Function Measurements in Cystic Fibrosis (CF) Patients before and after Treatment for a Pulmonary Exacerbation
  75. Vocal Cord Dysfunction Syndrome and “Steroid-Dependent” Asthmatics
  76. 486 Defective antibody-mediated opsonization of pseudomonas aeruginosa (PA) in cystic fibrosis (CF): An isotype-dependent deffect?
  77. 493 Suppression of the Late Cutaneous Response (LCR) by immunotherapy (IT)
  78. 282 A quantitative immunoenzymatic assay for grass pollen-specific IgG antibodies
  79. 8 Once a day theophylline (uniphyl) for treatment of patients with asthma (AS) and cystic fibrosis(CF)
  80. 124 Grass pollen immunotherapy, clinical and immunologic effects in a double-blind placebo-controlled study
  81. 37 Infantile allergy and milk-specific antibodies in breast milk