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The Role of Short-Chain Fatty Acids, Produced by Anaerobic Bacteria, in the Cystic Fibrosis Airway

American journal of respiratory and critical care medicine, 2015-12, Vol.192 (11), p.1314-1324

2015

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The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6-11 with cystic fibrosis in a real-world setting

Respiratory research, 2023-08, Vol.24 (1), p.199-199, Article 199

2023

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A role for whey acidic protein four-disulfide-core 12 (WFDC12) in the regulation of the inflammatory response in the lung

Thorax, 2015-05, Vol.70 (5), p.426-432

2015

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Appearance of Pancreatic Sufficiency and Discontinuation of Pancreatic Enzyme Replacement Therapy in Children with Cystic Fibrosis on Ivacaftor

Annals of the American Thoracic Society, 2021-01, Vol.18 (1), p.182-183

2021

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Apples to apples? Comparative analyses of national CF registries

Thorax, 2022-02, Vol.77 (2), p.112

2022

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Reply to Dournes and Benlala: Hierarchical Computed Tomography Scoring Systems Cannot Discriminate Between Reversible Bronchiectasis and Mucus Plugs

American journal of respiratory and critical care medicine, 2024-04, Vol.209 (8), p.1039

2024

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Six-lobe bronchoalveolar lavage in children with cystic fibrosis

The lancet respiratory medicine, 2018-10, Vol.6 (10), p.e51-e51

2018

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Role of extracellular vesicles in chronic lung disease

Thorax, 2021-10, Vol.76 (10), p.1047

2021

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Lower Airway Infection in Preschool Children with Cystic Fibrosis: An International Comparison

American journal of respiratory and critical care medicine, 2020-03, Vol.201 (6), p.748-750

2020

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Efficacy and adherence of noninvasive ventilation treatment in children with Down syndrome

Pediatric pulmonology, 2021-06, Vol.56 (6), p.1704-1715

2021

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Investigating serum extracellular vesicles in Cystic Fibrosis

Journal of cystic fibrosis, 2023-07, Vol.22 (4), p.674-679

2023

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Ivacaftor and Airway Inflammation in Preschool Children with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2021-09, Vol.204 (5), p.605-608

2021

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Pediatric invasive long‐term ventilation—A 10‐year review

Pediatric pulmonology, 2021-10, Vol.56 (10), p.3410-3416

2021

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Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged ⩾6 Years with Cystic Fibrosis and at Least One F508del Allele: A Phase 3, Open-Label Clinical Trial

American journal of respiratory and critical care medicine, 2023-07, Vol.208 (1), p.68

2023

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Update on Clinical Outcomes of Highly Effective Modulator Therapy

Clinics in chest medicine, 2022-12, Vol.43 (4), p.677-695

2022

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miR-17 overexpression in cystic fibrosis airway epithelial cells decreases interleukin-8 production

The European respiratory journal, 2015-11, Vol.46 (5), p.1350-1360

2015

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Anaerobic bacteria cultured from cystic fibrosis airways correlate to milder disease: a multisite study

The European respiratory journal, 2018-07, Vol.52 (1), p.1800242-1800242

2018

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miR-31 Dysregulation in Cystic Fibrosis Airways Contributes to Increased Pulmonary Cathepsin S Production

American journal of respiratory and critical care medicine, 2014-07, Vol.190 (2), p.165-174

2014

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Longitudinal Trends in Real-World Outcomes after Initiation of Ivacaftor. A Cohort Study from the Cystic Fibrosis Registry of Ireland

Annals of the American Thoracic Society, 2019-02, Vol.16 (2), p.209-216

2019

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Active video games as an exercise tool for children with cystic fibrosis

Journal of cystic fibrosis, 2014-05, Vol.13 (3), p.341-346

2014

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The findings of a clinical surveillance bronchoalveolar lavage programme in pre-school patients with cystic fibrosis

Pediatric pulmonology, 2015-04, Vol.50 (4), p.327-332

2015

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Tracheostomy speaking valve modification in children: A standardized approach leads to widespread use

Pediatric pulmonology, 2019-04, Vol.54 (4), p.428-435

2019

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Resolvin D1 regulates epithelial ion transport and inflammation in cystic fibrosis airways

Journal of cystic fibrosis, 2018-09, Vol.17 (5), p.607-615

2018

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The benefit of taking a control sample when performing bronchoalveolar lavage

Thorax, 2015-10, Vol.70 (10), p.990-990

2015

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The Role of Short-Chain Fatty Acids, Produced by Anaerobic Bacteria, in the Cystic Fibrosis Airway

The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6-11 with cystic fibrosis in a real-world setting

A role for whey acidic protein four-disulfide-core 12 (WFDC12) in the regulation of the inflammatory response in the lung

Appearance of Pancreatic Sufficiency and Discontinuation of Pancreatic Enzyme Replacement Therapy in Children with Cystic Fibrosis on Ivacaftor

Apples to apples? Comparative analyses of national CF registries

Reply to Dournes and Benlala: Hierarchical Computed Tomography Scoring Systems Cannot Discriminate Between Reversible Bronchiectasis and Mucus Plugs

Six-lobe bronchoalveolar lavage in children with cystic fibrosis

Role of extracellular vesicles in chronic lung disease

Lower Airway Infection in Preschool Children with Cystic Fibrosis: An International Comparison

Efficacy and adherence of noninvasive ventilation treatment in children with Down syndrome

Investigating serum extracellular vesicles in Cystic Fibrosis

Ivacaftor and Airway Inflammation in Preschool Children with Cystic Fibrosis

Pediatric invasive long‐term ventilation—A 10‐year review

Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged ⩾6 Years with Cystic Fibrosis and at Least One F508del Allele: A Phase 3, Open-Label Clinical Trial

Update on Clinical Outcomes of Highly Effective Modulator Therapy

miR-17 overexpression in cystic fibrosis airway epithelial cells decreases interleukin-8 production

Anaerobic bacteria cultured from cystic fibrosis airways correlate to milder disease: a multisite study

miR-31 Dysregulation in Cystic Fibrosis Airways Contributes to Increased Pulmonary Cathepsin S Production

Longitudinal Trends in Real-World Outcomes after Initiation of Ivacaftor. A Cohort Study from the Cystic Fibrosis Registry of Ireland

Active video games as an exercise tool for children with cystic fibrosis

The findings of a clinical surveillance bronchoalveolar lavage programme in pre-school patients with cystic fibrosis

Tracheostomy speaking valve modification in children: A standardized approach leads to widespread use

Resolvin D1 regulates epithelial ion transport and inflammation in cystic fibrosis airways

The natural history of cystic fibrosis liver disease a prospective cohort study

The benefit of taking a control sample when performing bronchoalveolar lavage

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