The impact of on lung disease in young children with cystic fibrosis is uncertain.To determine if positive respiratory cultures of species are associated with: (1) increased structural lung injury at age 5 years; (2) accelerated lung function decline between ages 5 years and 14 years and (3) to identify explanatory variables.A cross-sectional analysis of association between positive bronchoalveolar lavage (BAL) cultures and chest high-resolution CT (HRCT) scan findings at age 5 years in subjects from the Australasian Cystic Fibrosis Bronchoalveolar Lavage (ACFBAL) study was performed. A non-linear mixed-effects disease progression model was developed using FEV% predicted measurements at age 5 years from the ACFBAL study and at ages 6-14 yea...
Background: Cystic fibrosis (CF) is characterised by reduced airway clearance, microbial accumulatio...
Background: Computed tomography (CT) is used to monitor progression of structural lung disease (SLD)...
Little is known about early predictors of later cystic fibrosis (CF) structural lung disease. This s...
Rationale: Recent data show that Aspergillus species are prevalent respiratory infections in childre...
Background. The clinical relevance of Aspergillus fumigatus (Af) in cystic fibrosis (CF) is controve...
Background. The clinical relevance of Aspergillus fumigatus (Af) in cystic fibrosis (CF) is controve...
Filamentous fungi are commonly isolated from the respiratory tract of CF patients, but their clinica...
While detection rates in adults, adolescents and older children with cystic fibrosis (CF) have incre...
Lung disease in cystic fibrosis (CF) starts early, with studies identifying abnormalities on chest c...
Background: We hypothesized that the inflammatory response in the lungs of children with cystic fibr...
Objective To evaluate the effect of allergic bronchopulmonary aspergillosis (ABPA) on FEV1 percent p...
AbstractAspergillus fumigatus is commonly found in the respiratory secretions of patients with cysti...
BACKGROUND: Functional deterioration in cystic fibrosis (CF) may be reflected by increasing bronchia...
Rationale: Pulmonary inflammation, infection, and structural lung disease occur early in life in chi...
To identify potential risk factors for lung disease progression in children with cystic fibrosis (CF...
Background: Cystic fibrosis (CF) is characterised by reduced airway clearance, microbial accumulatio...
Background: Computed tomography (CT) is used to monitor progression of structural lung disease (SLD)...
Little is known about early predictors of later cystic fibrosis (CF) structural lung disease. This s...
Rationale: Recent data show that Aspergillus species are prevalent respiratory infections in childre...
Background. The clinical relevance of Aspergillus fumigatus (Af) in cystic fibrosis (CF) is controve...
Background. The clinical relevance of Aspergillus fumigatus (Af) in cystic fibrosis (CF) is controve...
Filamentous fungi are commonly isolated from the respiratory tract of CF patients, but their clinica...
While detection rates in adults, adolescents and older children with cystic fibrosis (CF) have incre...
Lung disease in cystic fibrosis (CF) starts early, with studies identifying abnormalities on chest c...
Background: We hypothesized that the inflammatory response in the lungs of children with cystic fibr...
Objective To evaluate the effect of allergic bronchopulmonary aspergillosis (ABPA) on FEV1 percent p...
AbstractAspergillus fumigatus is commonly found in the respiratory secretions of patients with cysti...
BACKGROUND: Functional deterioration in cystic fibrosis (CF) may be reflected by increasing bronchia...
Rationale: Pulmonary inflammation, infection, and structural lung disease occur early in life in chi...
To identify potential risk factors for lung disease progression in children with cystic fibrosis (CF...
Background: Cystic fibrosis (CF) is characterised by reduced airway clearance, microbial accumulatio...
Background: Computed tomography (CT) is used to monitor progression of structural lung disease (SLD)...
Little is known about early predictors of later cystic fibrosis (CF) structural lung disease. This s...