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Effects of maternal smoking during pregnancy and a family history of asthma on respiratory function in newborn infants

The Lancet (British edition), 1996-10, Vol.348 (9034), p.1060-1064

1996

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Feasibility of parental collected nasal swabs for virus detection in young children with cystic fibrosis

Journal of cystic fibrosis, 2014-12, Vol.13 (6), p.661-666

2014

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Control of breathing in infants born to smoking mothers

The Journal of pediatrics, 1999-08, Vol.135 (2), p.226-232

1999

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266 ‘Arresting’ psychological issues for better health outcomes in parents of infants and young children with cystic fibrosis

Journal of cystic fibrosis, 2014-06, Vol.13, p.S116-S116

2014

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P182 Prevalence of tracheobronchomalacia is higher than previously reported in children with cystic fibrosis

Journal of cystic fibrosis, 2023-06, Vol.22, p.S120-S120

2023

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51: ASSESSING PHAGE RESISTANCE EVOLUTION BY DISTINCT PSEUDOMONAS AERUGINOSA ISOLATES FROM INDIVIDUALS WITH CYSTIC FIBROSIS

Journal of global antimicrobial resistance., 2022-12, Vol.31, p.S31-S31

2022

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436: Effects of rhinovirus on airway-associated mucins in young children with cystic fibrosis

Journal of cystic fibrosis, 2021-11, Vol.20, p.S205

2021

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577: Outcomes from COMBAT CF: A phase 3 multicenter, randomized, placebo-controlled trial of azithromycin in primary prevention of radiologically defined bronchiectasis in infants with cystic fibrosis

Journal of cystic fibrosis, 2021-11, Vol.20, p.S274

2021

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521: Epithelial Mesenchymal Transition (EMT) in Bronchiolitis Obliterans Syndrome (BOS) Is Not Restricted to Small Airways

The Journal of heart and lung transplantation, 2009-02, Vol.28 (2), p.S246-S247

2009

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430 Ivacaftor treatment decreases prevalence of insoluble mucus flakes in young people with cystic fibrosis

Journal of cystic fibrosis, 2022-10, Vol.21, p.S247-S248

2022

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CT-detected early structural lung disease is progressive in infants and preschool children

Journal of cystic fibrosis, 2009, Vol.8, p.S68-S68

2009

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Novel broad-spectrum peptide therapy reverses respiratory infections with multidrug-resistant gram-negative bacteria

International journal of antimicrobial agents, 2021-09, Vol.58, p.21002983, Article 21002983

2021

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Novel non-invasive point of care sputum test for early identification of Pseudomonas aeruginosa airway infection

International journal of antimicrobial agents, 2021-09, Vol.58, p.21003381, Article 21003381

2021

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CD14 C-159T and early infection with Pseudomonas aeruginosa in children with cystic fibrosis

Respiratory research, 2005-06, Vol.6 (1), p.63-63, Article 63

2005

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354: Roles of mucus concentration and composition in disfunction mucociliary clearance in cystic fibrosis

Journal of cystic fibrosis, 2021-11, Vol.20, p.S168-S169

2021

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576: Ivacaftor treatment alters the relationship between mucoinflammation and structural lung disease in preschool-aged children with CF

Journal of cystic fibrosis, 2021-11, Vol.20, p.S273

2021

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489: Relationships between antibiotic exposure and early lung microbial colonization in infants with cystic fibrosis

Journal of cystic fibrosis, 2021-11, Vol.20, p.S231

2021

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414 Longitudinal analysis of early-life bronchoalveolar fluid identifies immune mediators associated with bronchiectasis risk in children with cystic fibrosis

Journal of cystic fibrosis, 2022-10, Vol.21, p.S240-S240

2022

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WS12.03 PD-1 expression on airway macrophages in early cystic fibrosis lung disease coincides with decreased expression of phagocytosis-related markers

Journal of cystic fibrosis, 2022-06, Vol.21, p.S23

2022

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377: Airway macrophages in early CF lung disease show signs of immune paralysis

Journal of cystic fibrosis, 2021-11, Vol.20, p.S178-S179

2021

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488: Bile acids, bacterial colonization, and lung inflammatory markers in infants with cystic fibrosis

Journal of cystic fibrosis, 2021-11, Vol.20, p.S230-S231

2021

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348: Pseudomonas aeruginosa infection modulates primary granule exocytosis

Journal of cystic fibrosis, 2021-11, Vol.20, p.S166-S167

2021

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386 Association between myeloperoxidase activity and methionine oxidation products in bronchoalveolar lavage and risk of bronchiectasis in infants and toddlers with cystic fibrosis

Journal of cystic fibrosis, 2022-10, Vol.21, p.S226-S226

2022

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446 Metabolites in early life bronchoalveolar fluid associate with future bronchiectasis risk in children with cystic fibrosis

Journal of cystic fibrosis, 2022-10, Vol.21, p.S256-S256

2022

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P058 The effect of hypertonic saline treatment in pre-schoolers with cystic fibrosis on lung structure as measured by chest computed tomography. SHIP-CT study

Journal of cystic fibrosis, 2021, Vol.20, p.S56

2021

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Effects of maternal smoking during pregnancy and a family history of asthma on respiratory function in newborn infants

Feasibility of parental collected nasal swabs for virus detection in young children with cystic fibrosis

Control of breathing in infants born to smoking mothers

266 ‘Arresting’ psychological issues for better health outcomes in parents of infants and young children with cystic fibrosis

P182 Prevalence of tracheobronchomalacia is higher than previously reported in children with cystic fibrosis

51: ASSESSING PHAGE RESISTANCE EVOLUTION BY DISTINCT PSEUDOMONAS AERUGINOSA ISOLATES FROM INDIVIDUALS WITH CYSTIC FIBROSIS

436: Effects of rhinovirus on airway-associated mucins in young children with cystic fibrosis

577: Outcomes from COMBAT CF: A phase 3 multicenter, randomized, placebo-controlled trial of azithromycin in primary prevention of radiologically defined bronchiectasis in infants with cystic fibrosis

521: Epithelial Mesenchymal Transition (EMT) in Bronchiolitis Obliterans Syndrome (BOS) Is Not Restricted to Small Airways

430 Ivacaftor treatment decreases prevalence of insoluble mucus flakes in young people with cystic fibrosis

CT-detected early structural lung disease is progressive in infants and preschool children

Novel broad-spectrum peptide therapy reverses respiratory infections with multidrug-resistant gram-negative bacteria

Novel non-invasive point of care sputum test for early identification of Pseudomonas aeruginosa airway infection

CD14 C-159T and early infection with Pseudomonas aeruginosa in children with cystic fibrosis

354: Roles of mucus concentration and composition in disfunction mucociliary clearance in cystic fibrosis

576: Ivacaftor treatment alters the relationship between mucoinflammation and structural lung disease in preschool-aged children with CF

489: Relationships between antibiotic exposure and early lung microbial colonization in infants with cystic fibrosis

414 Longitudinal analysis of early-life bronchoalveolar fluid identifies immune mediators associated with bronchiectasis risk in children with cystic fibrosis

WS12.03 PD-1 expression on airway macrophages in early cystic fibrosis lung disease coincides with decreased expression of phagocytosis-related markers

377: Airway macrophages in early CF lung disease show signs of immune paralysis

488: Bile acids, bacterial colonization, and lung inflammatory markers in infants with cystic fibrosis

348: Pseudomonas aeruginosa infection modulates primary granule exocytosis

386 Association between myeloperoxidase activity and methionine oxidation products in bronchoalveolar lavage and risk of bronchiectasis in infants and toddlers with cystic fibrosis

446 Metabolites in early life bronchoalveolar fluid associate with future bronchiectasis risk in children with cystic fibrosis

P058 The effect of hypertonic saline treatment in pre-schoolers with cystic fibrosis on lung structure as measured by chest computed tomography. SHIP-CT study

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