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Lung microbiota across age and disease stage in cystic fibrosis

Scientific reports, 2015-05, Vol.5 (1), p.10241-10241, Article 10241

2015

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Selective Sweeps and Parallel Pathoadaptation Drive Pseudomonas aeruginosa Evolution in the Cystic Fibrosis Lung

mBio, 2015-09, Vol.6 (5), p.e00981-e00915

2015

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Global Analysis of the Fungal Microbiome in Cystic Fibrosis Patients Reveals Loss of Function of the Transcriptional Repressor Nrg1 as a Mechanism of Pathogen Adaptation

PLoS pathogens, 2015-11, Vol.11 (11), p.e1005308-e1005308

2015

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Phenotypic diversity within a Pseudomonas aeruginosa population infecting an adult with cystic fibrosis

Scientific reports, 2015-06, Vol.5 (1), p.10932-10932, Article 10932

2015

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Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor

Journal of cystic fibrosis, 2018-01, Vol.17 (1), p.83-88

2018

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Analysis of the cystic fibrosis lung microbiota via serial Illumina sequencing of bacterial 16S rRNA hypervariable regions

PloS one, 2012-10, Vol.7 (10), p.e45791-e45791

2012

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A genome-wide association analysis reveals a potential role for recombination in the evolution of antimicrobial resistance in Burkholderia multivorans

PLoS pathogens, 2018-12, Vol.14 (12), p.e1007453-e1007453

2018

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Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass

Frontiers in pharmacology, 2023-07, Vol.14, p.1157459-1157459

2023

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Genomic epidemiology of Mycobacterium abscessus in a Canadian cystic fibrosis centre

Scientific reports, 2022-09, Vol.12 (1), p.16116-16116, Article 16116

2022

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Functional integrity in children with anoxic brain injury from drowning

Human brain mapping, 2017-10, Vol.38 (10), p.4813-4831

2017

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Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations

NPJ biofilms and microbiomes, 2019-01, Vol.5 (1), p.4-4, Article 4

2019

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Management of pregnancy in cystic fibrosis

Breathe (Lausanne, Switzerland), 2022-06, Vol.18 (2), p.220005-220005

2022

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Clinical development of triple-combination CFTR modulators for cystic fibrosis patients with one or two F508del alleles

ERJ open research, 2019-04, Vol.5 (2), p.82

2019

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Treatment of Aspergillus fumigatus in patients with cystic fibrosis: a randomized, placebo-controlled pilot study

PloS one, 2012-04, Vol.7 (4), p.e36077-e36077

2012

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High-flow nasal oxygen versus noninvasive ventilation in adult patients with cystic fibrosis: a randomized crossover physiological study

Annals of intensive care, 2018-09, Vol.8 (1), p.85-9, Article 85

2018

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Gaps in the inpatient management of chronic obstructive pulmonary disease exacerbation and impact of an evidence-based order set

Canadian respiratory journal, 2015-05, Vol.22 (3), p.157-162

2015

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Epidemiology of Clonal Pseudomonas aeruginosa Infection in a Canadian Cystic Fibrosis Population

Annals of the American Thoracic Society, 2018-07, Vol.15 (7), p.827-836

2018

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Clinical Manifestations of Cystic Fibrosis Among Patients With Diagnosis in Adulthood

Chest, 2004-10, Vol.126 (4), p.1215-1224

2004

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Fourier Transform Infrared Spectroscopy for Typing Burkholderia cenocepacia ET12 Isolates

Microbiology spectrum, 2021-12, Vol.9 (3), p.e0183121-e0183121

2021

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Prevalence of Vertebral Fractures in Adults With Cystic Fibrosis and Their Relationship to Bone Mineral Density

Chest, 2006-08, Vol.130 (2), p.539-544

2006

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Clinical Outcomes Associated with Achromobacter Species Infection in Patients with Cystic Fibrosis

Annals of the American Thoracic Society, 2017-09, Vol.14 (9), p.1412-1418

2017

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Human neutrophil peptides induce interleukin-8 production through the P2Y6 signaling pathway

Blood, 2006-04, Vol.107 (7), p.2936-2942

2006

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Significant differences in type IV pilin allele distribution among Pseudomonas aeruginosa isolates from cystic fibrosis (CF) versus non-CF patients

Microbiology (Society for General Microbiology), 2004-05, Vol.150 (Pt 5), p.1315

2004

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Lung microbiota across age and disease stage in cystic fibrosis

The future of cystic fibrosis care: a global perspective

Selective Sweeps and Parallel Pathoadaptation Drive Pseudomonas aeruginosa Evolution in the Cystic Fibrosis Lung

Global Analysis of the Fungal Microbiome in Cystic Fibrosis Patients Reveals Loss of Function of the Transcriptional Repressor Nrg1 as a Mechanism of Pathogen Adaptation

Phenotypic diversity within a Pseudomonas aeruginosa population infecting an adult with cystic fibrosis

Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor

Analysis of the cystic fibrosis lung microbiota via serial Illumina sequencing of bacterial 16S rRNA hypervariable regions

A genome-wide association analysis reveals a potential role for recombination in the evolution of antimicrobial resistance in Burkholderia multivorans

Weight increase in people with cystic fibrosis on CFTR modulator therapy is mainly due to increase in fat mass

Genomic epidemiology of Mycobacterium abscessus in a Canadian cystic fibrosis centre

Functional integrity in children with anoxic brain injury from drowning

Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations

Management of pregnancy in cystic fibrosis

Clinical development of triple-combination CFTR modulators for cystic fibrosis patients with one or two F508del alleles

Treatment of Aspergillus fumigatus in patients with cystic fibrosis: a randomized, placebo-controlled pilot study

High-flow nasal oxygen versus noninvasive ventilation in adult patients with cystic fibrosis: a randomized crossover physiological study

Gaps in the inpatient management of chronic obstructive pulmonary disease exacerbation and impact of an evidence-based order set

Epidemiology of Clonal Pseudomonas aeruginosa Infection in a Canadian Cystic Fibrosis Population

Clinical Manifestations of Cystic Fibrosis Among Patients With Diagnosis in Adulthood

Fourier Transform Infrared Spectroscopy for Typing Burkholderia cenocepacia ET12 Isolates

Prevalence of Vertebral Fractures in Adults With Cystic Fibrosis and Their Relationship to Bone Mineral Density

Clinical Outcomes Associated with Achromobacter Species Infection in Patients with Cystic Fibrosis

Human neutrophil peptides induce interleukin-8 production through the P2Y6 signaling pathway

High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification

Significant differences in type IV pilin allele distribution among Pseudomonas aeruginosa isolates from cystic fibrosis (CF) versus non-CF patients

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