International audienceSeveral predictive models have been proposed to understand the microbial risk factors associated with cystic fibrosis (CF) progression. Very few have integrated fungal airways colonisation, which is increasingly recognized as a key player regarding CF progression. To assess the association between the percent predicted forced expiratory volume in 1 s (ppFEV1) change and the fungi or bacteria identified in the sputum, 299 CF patients from the “MucoFong” project were included and followed-up with over two years. The relationship between the microorganisms identified in the sputum and ppFEV1 course of patients was longitudinally analysed. An adjusted linear mixed model analysis was performed to evaluate the effect of a tr...
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the gene encoding the ...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
Although anaerobic bacteria exist in abundance in cystic fibrosis (CF) airways, their role in diseas...
Several predictive models have been proposed to understand the microbial risk factors associated wit...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
<div><p>Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of t...
Rationale Pulmonary infections with nontuberculous mycobacteria (NTM) are increasingly prevalent in ...
<p>The airways of patients with CF are colonized from various host (as indicated) and environmental ...
The defective mucociliary clearance due to CFTR malfunctioning causes predisposition to the coloniza...
Introduction and Objectives The microbial communities present in CF sputum are polymicrobial and c...
The respiratory mycobiome is an important but understudied component of the human microbiota. Like b...
International audienceLung infections play a critical role in cystic fibrosis (CF) pathogenesis. CF ...
Background: Chronic infection and concomitant airway inflammation is the leading cause of morbidity ...
Background: Pulmonary exacerbations (PEx), frequently associated with airway infection and inflammat...
Pulmonary exacerbations (PEx), frequently associated with airway infection and inflammation, are the...
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the gene encoding the ...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
Although anaerobic bacteria exist in abundance in cystic fibrosis (CF) airways, their role in diseas...
Several predictive models have been proposed to understand the microbial risk factors associated wit...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
<div><p>Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of t...
Rationale Pulmonary infections with nontuberculous mycobacteria (NTM) are increasingly prevalent in ...
<p>The airways of patients with CF are colonized from various host (as indicated) and environmental ...
The defective mucociliary clearance due to CFTR malfunctioning causes predisposition to the coloniza...
Introduction and Objectives The microbial communities present in CF sputum are polymicrobial and c...
The respiratory mycobiome is an important but understudied component of the human microbiota. Like b...
International audienceLung infections play a critical role in cystic fibrosis (CF) pathogenesis. CF ...
Background: Chronic infection and concomitant airway inflammation is the leading cause of morbidity ...
Background: Pulmonary exacerbations (PEx), frequently associated with airway infection and inflammat...
Pulmonary exacerbations (PEx), frequently associated with airway infection and inflammation, are the...
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the gene encoding the ...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
Although anaerobic bacteria exist in abundance in cystic fibrosis (CF) airways, their role in diseas...