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Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations

PloS one, 2013-04, Vol.8 (4), p.e62917-e62917

2013

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Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

The Journal of pediatrics, 2008-08, Vol.153 (2), p.S4-S14

2008

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Diagnosis of Cystic Fibrosis in Screened Populations

The Journal of pediatrics, 2017-02, Vol.181, p.S33-S44.e2

2017

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Molecular identification of bacteria in bronchoalveolar lavage fluid from children with cystic fibrosis

Proceedings of the National Academy of Sciences - PNAS, 2007-12, Vol.104 (51), p.20529-20533

2007

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Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis

The Journal of pediatrics, 2009-12, Vol.155 (6), p.S73-S93

2009

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Molecular Identification of Staphylococcus aureus in Airway Samples from Children with Cystic Fibrosis

PloS one, 2016-01, Vol.11 (1), p.e0147643-e0147643

2016

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Cystic Fibrosis Foundation Practice Guidelines for the Management of Infants with Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome during the First Two Years of Life and Beyond

The Journal of pediatrics, 2009-12, Vol.155 (6), p.S106-S116

2009

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Reliability of quantitative real-time PCR for bacterial detection in cystic fibrosis airway specimens

PloS one, 2010-11, Vol.5 (11), p.e15101

2010

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Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation

PloS one, 2013-07, Vol.8 (7), p.e66955

2013

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Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection

PloS one, 2017-05, Vol.12 (5), p.e0177215-e0177215

2017

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Evaluation of circulating proteins and hemodynamics towards predicting mortality in children with pulmonary arterial hypertension

PloS one, 2013-11, Vol.8 (11), p.e80235-e80235

2013

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Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections

American journal of respiratory and critical care medicine, 2017-06, Vol.195 (12), p.1617-1628

2017

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Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis

BMC pulmonary medicine, 2017-12, Vol.17 (1), p.188-188, Article 188

2017

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Airway microbiota across age and disease spectrum in cystic fibrosis

The European respiratory journal, 2017-11, Vol.50 (5), p.1700832-1700832

2017

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Entering the era of highly effective CFTR modulator therapy

The Lancet (British edition), 2019-11, Vol.394 (10212), p.1886-1888

2019

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Airway Inflammation in Children with Cystic Fibrosis and Healthy Children Assessed by Sputum Induction

American journal of respiratory and critical care medicine, 2001-10, Vol.164 (8), p.1425-1431

2001

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Preterm Birth and Airway Inflammation in Childhood

The Journal of pediatrics, 2012-12, Vol.161 (6), p.979-980

2012

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Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis

Nature communications, 2015-09, Vol.6 (1), p.8382-8382, Article 8382

2015

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Treatment of cystic fibrosis in infants

The lancet respiratory medicine, 2018-07, Vol.6 (7), p.483-484

Accurso, Frank J

2018

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A New Cystic Fibrosis Newborn Screening Algorithm: IRT/IRT1↑/DNA

The Journal of pediatrics, 2009-11, Vol.155 (5), p.618-622

2009

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Circulating Cytokines and Growth Factors in Pediatric Pulmonary Hypertension

Mediators of Inflammation, 2012-01, Vol.2012, p.143428-7

2012

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Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTR Mutation

The New England journal of medicine, 2010-11, Vol.363 (21), p.1991-2003

2010

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Assessment of airway microbiota and inflammation in cystic fibrosis using multiple sampling methods

Annals of the American Thoracic Society, 2015-02, Vol.12 (2), p.221-229

2015

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Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations

Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

Diagnosis of Cystic Fibrosis in Screened Populations

Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial

Molecular identification of bacteria in bronchoalveolar lavage fluid from children with cystic fibrosis

Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis

Molecular Identification of Staphylococcus aureus in Airway Samples from Children with Cystic Fibrosis

Cystic Fibrosis Foundation Practice Guidelines for the Management of Infants with Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome during the First Two Years of Life and Beyond

Reliability of quantitative real-time PCR for bacterial detection in cystic fibrosis airway specimens

Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation

Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection

Evaluation of circulating proteins and hemodynamics towards predicting mortality in children with pulmonary arterial hypertension

Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections

Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis

Airway microbiota across age and disease spectrum in cystic fibrosis

Entering the era of highly effective CFTR modulator therapy

Airway Inflammation in Children with Cystic Fibrosis and Healthy Children Assessed by Sputum Induction

Preterm Birth and Airway Inflammation in Childhood

Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis

Treatment of cystic fibrosis in infants

A New Cystic Fibrosis Newborn Screening Algorithm: IRT/IRT1↑/DNA

Circulating Cytokines and Growth Factors in Pediatric Pulmonary Hypertension

Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation

Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTR Mutation

Assessment of airway microbiota and inflammation in cystic fibrosis using multiple sampling methods

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