Objectives The aim of the present study was to determine whether adult CF patients with pulmonary NTM infection have worse clinical outcomes, when compared to a matched group of CF patients who have never had NTM isolated. Additionally, the study also aims to determine what proportion of the overall bacterial community is NTM compared to other bacteria. Method Clinical data were collected from 12 spontaneously expec-torating CF patients who cultured M abscessus in the sputum since they were first infected with M abscessus, and 24 matched controls who have CF, but never been infected with M abscessus. Student unpaired t-test was used to compare the mean forced expiratory volume (FEV1) per year between the two groups. Results Data from 36 ind...
Introduction: In CF, infective pulmonary exacerbations are common. Despite this, significant aspects...
The aim of this study was to investigate the polymicrobial communities in an adult Cystic Fibrosis p...
Pulmonary deterioration has remained the major cause of mortality in cystic fibrosis (C17) patients ...
Introduction and Objectives The microbial communities present in CF sputum are polymicrobial and c...
Rationale Pulmonary infections with nontuberculous mycobacteria (NTM) are increasingly prevalent in ...
Although nontuberculous mycobacteria (NTM) are recognized pathogens in cystic fibrosis (CF), associa...
Several predictive models have been proposed to understand the microbial risk factors associated wit...
The prevalence of nontuberculous mycobacteria (NTM) is high (approximately 13%) in sputum of patient...
Nontuberculous mycobacteria (NTM) are potential respiratory pathogens in cystic fibrosis (CF). To as...
<div><p>Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of t...
AbstractBackgroundAlthough nontuberculous mycobacteria (NTM) are recognized pathogens in cystic fibr...
<p>The airways of patients with CF are colonized from various host (as indicated) and environmental ...
<div><p>Background</p><p>Routine clinical diagnostics of CF patients focus only on a restricted set ...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
The respiratory mycobiome is an important but understudied component of the human microbiota. Like b...
Introduction: In CF, infective pulmonary exacerbations are common. Despite this, significant aspects...
The aim of this study was to investigate the polymicrobial communities in an adult Cystic Fibrosis p...
Pulmonary deterioration has remained the major cause of mortality in cystic fibrosis (C17) patients ...
Introduction and Objectives The microbial communities present in CF sputum are polymicrobial and c...
Rationale Pulmonary infections with nontuberculous mycobacteria (NTM) are increasingly prevalent in ...
Although nontuberculous mycobacteria (NTM) are recognized pathogens in cystic fibrosis (CF), associa...
Several predictive models have been proposed to understand the microbial risk factors associated wit...
The prevalence of nontuberculous mycobacteria (NTM) is high (approximately 13%) in sputum of patient...
Nontuberculous mycobacteria (NTM) are potential respiratory pathogens in cystic fibrosis (CF). To as...
<div><p>Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of t...
AbstractBackgroundAlthough nontuberculous mycobacteria (NTM) are recognized pathogens in cystic fibr...
<p>The airways of patients with CF are colonized from various host (as indicated) and environmental ...
<div><p>Background</p><p>Routine clinical diagnostics of CF patients focus only on a restricted set ...
Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airwa...
The respiratory mycobiome is an important but understudied component of the human microbiota. Like b...
Introduction: In CF, infective pulmonary exacerbations are common. Despite this, significant aspects...
The aim of this study was to investigate the polymicrobial communities in an adult Cystic Fibrosis p...
Pulmonary deterioration has remained the major cause of mortality in cystic fibrosis (C17) patients ...