Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis. - sprookjes - yvandenbroek - TriplyDB

Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis.

Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis.

http://www.wikidata.org/entity/Q44001744

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The Role of Computed Tomography in Monitoring Patients with Cystic Fibrosis The Evolution of Cystic Fibrosis Care Is chest CT useful in newborn screened infants with cystic fibrosis at 1 year of age?Determining cystic fibrosis-affected lung microbiology: comparison of spontaneous and serially induced sputum samples by use of terminal restriction fragment length polymorphism profiling.Characterizing Lung Disease in Cystic Fibrosis with Magnetic Resonance Imaging and Airway Physiology.Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection.Cystic fibrosis: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases.Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening.Lessons learned from a randomized trial of airway secretion clearance techniques in cystic fibrosis Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial.Effect of segmental bronchoalveolar lavage on quantitative computed tomography of the lung.Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints.Chronic productive cough and extensive cysts in left lung Regional differences in the evolution of lung disease in children with cystic fibrosis.Analysis of Lung Microbiota in Bronchoalveolar Lavage, Protected Brush and Sputum Samples from Subjects with Mild-To-Moderate Cystic Fibrosis Lung Disease.Exhaled breath condensate purines correlate with lung function in infants and preschoolers Airway Microbiota in Bronchoalveolar Lavage Fluid from Clinically Well Infants with Cystic Fibrosis.The correlation of brody high resolution computed tomography scoring system with clinical status and pulmonary function test in patients with cystic fibrosis.Exhaled breath condensate adenosine tracks lung function changes in cystic fibrosis.The porcine lung as a potential model for cystic fibrosis Endpoints for clinical trials in young children with cystic fibrosis.Update in cystic fibrosis 2007.Adult onset lung disease following transient disruption of fetal stretch-induced differentiation.Progress in cystic fibrosis and the CF Therapeutics Development Network Recruitment maneuvers for acute lung injury: a systematic review.Risk factors for the progression of cystic fibrosis lung disease throughout childhood.Assessment and monitoring of cystic fibrosis lung disease in infants and young children.Lung function distinguishes preschool children with CF from healthy controls in a multi-center setting.Novel end points for clinical trials in young children with cystic fibrosis Staphylococcus aureus in early cystic fibrosis lung disease.Effects of alveolar recruitment maneuvers on clinical outcomes in patients with acute respiratory distress syndrome: a systematic review and meta-analysis.Scoring of chest CT in children with cystic fibrosis: state of the art.What did we learn from two decades of chest computed tomography in cystic fibrosis?Early airway structural changes in cystic fibrosis pigs as a determinant of particle distribution and deposition.Respiratory tract exacerbations revisited: ventilation, inflammation, perfusion, and structure (VIPS) monitoring to redefine treatment.Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification.Diagnosis and early life risk factors for bronchiectasis in cystic fibrosis: a review.Special considerations for the treatment of pulmonary exacerbations in children with cystic fibrosis.Ultrashort Echo-Time Magnetic Resonance Imaging Is a Sensitive Method for the Evaluation of Early Cystic Fibrosis Lung Disease.Early pulmonary disease manifestations in cystic fibrosis mice.

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Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis.

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Computed tomography reflects l ...... nges in early cystic fibrosis.

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RCCM.200603-343OC

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American Journal of Respiratory and Critical Care Medicine

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Computed tomography reflects l ...... anges in early cystic fibrosis

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Alan S Brody

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Bahjat F Qaqish

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Bonnie C Yankaskas

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George Z Retsch-Bogart

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Margaret W Leigh

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Robin C Johnson

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Stephanie D Davis

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Terry L Noah

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P2860

Pulmonary disease assessment in cystic fibrosis: comparison of CT scoring systems and value of bronchial and arterial dimension measurements.

Progression of lung disease on computed tomography and pulmonary function tests in children and adults with cystic fibrosis.

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

Lower respiratory infection and inflammation in infants with newly diagnosed cystic fibrosis

High-resolution computed tomography imaging of airway disease in infants with cystic fibrosis

Gastroesophageal reflux in the infant with cystic fibrosis.

Gastroesophageal reflux and respiratory disease in children.

Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis.

High resolution computed tomography in cystic fibrosis: correlation with pulmonary function and assessment of prognostic value.

Spirometer-triggered high-resolution computed tomography and pulmonary function measurements during an acute exacerbation in patients with cystic fibrosis.

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cystic fibrosis