FAQ

Pulmonary Cystic Fibrosis

Known as: CYSTIC FIBROSIS LUNG, Cystic Fibrosis, Pulmonary, cystic fibrosis lungs 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1983-2017
024619832017

Related topics

Related topics

3 relations

Broader (3)

Cystic FibrosisLung diseasesairway disease

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Pulmonary Cystic Fibrosis
Lung diseases
Cystic Fibrosis
airway disease

Papers overview

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2014
2014
Adaptation of iron homeostasis pathways by a Pseudomonas aeruginosa pyoverdine mutant in the cystic fibrosis lung.
Cystic fibrosis (CF) patients suffer from chronic bacterial lung infections, most notably by Pseudomonas aeruginosa, which… (More)
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2012
2012
Description and validation of a scoring system for tomosynthesis in pulmonary cystic fibrosis
To design and validate a scoring system for tomosynthesis (digital tomography) in pulmonary cystic fibrosis. A scoring system… (More)
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2011
2011
Two-component regulatory systems in Pseudomonas aeruginosa: an intricate network mediating fimbrial and efflux pump gene expression
Pseudomonas aeruginosa is responsible for chronic and acute infections in humans. Chronic infections are associated with… (More)
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Highly Cited
2005
Highly Cited
2005
Microcolony formation: a novel biofilm model of Pseudomonas aeruginosa for the cystic fibrosis lung.
Pseudomonas aeruginosa colonizing the lung of cystic fibrosis patients is responsible for a decline in health and poor prognosis… (More)
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2005
2005
Proteome analysis reveals adaptation of Pseudomonas aeruginosa to the cystic fibrosis lung environment.
Pseudomonas aeruginosa is known for the chronic lung colonization of cystic fibrosis (CF) patients in addition to eye, ear and… (More)
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2003
2003
Impact of large chromosomal inversions on the adaptation and evolution of Pseudomonas aeruginosa chronically colonizing cystic fibrosis lungs.
Pseudomonas aeruginosa chronically colonizing the lungs of cystic fibrosis (CF) patients undergoes fast evolution leading to… (More)
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2002
2002
DeltaF508-CFTR causes constitutive NF-kappaB activation through an ER-overload response in cystic fibrosis lungs.
The clinical course of Cystic Fibrosis is characterized by recurrent pulmonary infections which ultimately lead to death by… (More)
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2000
2000
Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs.
It is not clear how airway pathology relates to the severity of airflow obstruction and increased bronchial responsiveness in… (More)
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Highly Cited
1995
Highly Cited
1995
Inflammatory cytokines in cystic fibrosis lungs.
Chronic pulmonary infection with Pseudomonas aeruginosa continues to be the major cause of morbidity and mortality in cystic… (More)
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1989
1989
High-resolution computed tomography in pulmonary cystic fibrosis.
Twenty-one patients with established cystic fibrosis were examined using high-resolution, narrow-section computed tomography. The… (More)
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