Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis. - Wikidata - wikimedia - TriplyDB

Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis.

Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis.

http://www.wikidata.org/entity/Q49147380

about

Mechanisms of the noxious inflammatory cycle in cystic fibrosis Microbiology of airway disease in a cohort of patients with cystic fibrosis.Pseudomonas aeruginosa inhibits endocytic recycling of CFTR in polarized human airway epithelial cells The Pseudomonas aeruginosa lipid A deacylase: selection for expression and loss within the cystic fibrosis airway.Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis.Contribution of Burkholderia cenocepacia flagella to infectivity and inflammation.Early anti-pseudomonal acquisition in young patients with cystic fibrosis: rationale and design of the EPIC clinical trial and observational study'Bdellovibrio bacteriovorus directly attacks Pseudomonas aeruginosa and Staphylococcus aureus Cystic fibrosis isolates.A pilot trial on safety and efficacy of erythrocyte-mediated steroid treatment in CF patients Unfractionated heparin reduces the elasticity of sputum from patients with cystic fibrosis.Proinflammatory phenotype and increased caveolin-1 in alveolar macrophages with silenced CFTR mRNA 2-Aminoacetophenone as a potential breath biomarker for Pseudomonas aeruginosa in the cystic fibrosis lung.Achromobacter xylosoxidans genomic characterization and correlation of randomly amplified polymorphic DNA profiles with relevant clinical features [corrected] of cystic fibrosis patients.Enhanced Pseudomonas aeruginosa biofilm development mediated by human neutrophils Neutrophil extracellular trap (NET)-mediated killing of Pseudomonas aeruginosa: evidence of acquired resistance within the CF airway, independent of CFTR.Expression of PPARγ and paraoxonase 2 correlated with Pseudomonas aeruginosa infection in cystic fibrosis.Estrogen aggravates inflammation in Pseudomonas aeruginosa pneumonia in cystic fibrosis mice.Clinical significance of microbial infection and adaptation in cystic fibrosis.Neutrophilic airway inflammation and IL-17.Pediatrics, surfactant, and cystic fibrosis in AJRCCM 2002.Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints.Correlation of forced oscillation technique in preschool children with cystic fibrosis with pulmonary inflammation Early airway infection, inflammation, and lung function in cystic fibrosis.Inflammatory markers of lung disease in adult patients with cystic fibrosis.Lung inflammation as a therapeutic target in cystic fibrosis.Future directions in early cystic fibrosis lung disease research: an NHLBI workshop report Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests Airway Microbiota in Bronchoalveolar Lavage Fluid from Clinically Well Infants with Cystic Fibrosis.New insights into pulmonary inflammation in cystic fibrosis.Distribution of sputum cellular phenotype in a large asthma cohort: predicting factors for eosinophilic vs neutrophilic inflammation Endpoints for clinical trials in young children with cystic fibrosis.Impact of Pseudomonas and Staphylococcus infection on inflammation and clinical status in young children with cystic fibrosis.Quantifying pulmonary inflammation in cystic fibrosis with positron emission tomography.Galectin-9 signaling through TIM-3 is involved in neutrophil-mediated Gram-negative bacterial killing: an effect abrogated within the cystic fibrosis lung.Eradication of early Pseudomonas infection in cystic fibrosis.Mechanism of fibroblast inflammatory responses to Pseudomonas aeruginosa elastase.Outbreak of Achromobacter xylosoxidans in an Italian Cystic fibrosis center: genome variability, biofilm production, antibiotic resistance, and motility in isolated strains.Lung function testing in preschool-aged children with cystic fibrosis in the clinical setting.Assessment and monitoring of cystic fibrosis lung disease in infants and young children.The cystic fibrosis neutrophil: a specialized yet potentially defective cell.

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P2860

Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis.

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American Journal of Respiratory and Critical Care Medicine

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Inflammation, infection, and p ...... children with cystic fibrosis.

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Andrew H Numa

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Calypso C Vertzyas

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Carolyn J Dakin

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He Wang

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John R Morton

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P2860

Pulmonary function in infants with cystic fibrosis: the effect of antibiotic treatment.

Multiple-breath nitrogen washout techniques: including measurements with patients on ventilators.

Serial lung function studies in cystic fibrosis in the first 5 years of life

Increased DNA levels in bronchoalveolar lavage fluid obtained from infants with cystic fibrosis.

Bronchoalveolar lavage as a research tool.

Cystic fibrosis. 1. Pseudomonas aeruginosa infection in cystic fibrosis and its management

Noninvasive determination of respiratory mechanics during mechanical ventilation of neonates: a review of current and future techniques.

Lung function in infants with cystic fibrosis

The effect of nebulized epinephrine on respiratory mechanics and gas exchange in bronchiolitis.

Immunohistopathologic localization of Pseudomonas aeruginosa in lungs from patients with cystic fibrosis. Implications for the pathogenesis of progressive lung deterioration.

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cystic fibrosis