Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis.

Respiratory research - 30 Nov 2006

Kraemer Richard, Baldwin David N, Ammann Roland A, Frey Urs, Gallati Sabina

Abstract excerpt

BACKGROUND: Functional deterioration in cystic fibrosis (CF) may be reflected by increasing bronchial obstruction and, as recently shown, by ventilation inhomogeneities. This study investigated which physiological factors (airway obstruction, ventilation inhomogeneities, pulmonary hyperinflation, development of trapped gas) best express the decline in lung function, and what role specific CFTR genotypes and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Cystic Fibrosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cystic Fibrosis Transmembrane Conductance Regulator

Share to Disease Progression

Share to Environmental Exposure

Share to Lung Diseases, Obstructive

Share to Registries

Share to Spirometry

Source

Open in PubMed Open full text

Identifiers

PMID: 17137500
DOI: 10.1186/1465-9921-7-138
PMCID: PMC1698484

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis.PMID 17137500Read ↗

Long-term gas exchange characteristics as markers of deterioration in patients with cystic fibrosis.Semantic proximity Read ↗

Cystic fibrosis lung disease: genetic influences, microbial interactions, and radiological assessment.Semantic proximity Read ↗

Pulmonary Physiology of Chronic Obstructive Pulmonary Disease, Cystic Fibrosis, and Alpha-1 Antitrypsin Deficiency.Semantic proximity Read ↗

Risk factors for the progression of cystic fibrosis lung disease throughout childhood.Semantic proximity Read ↗

Risk factors for lung function decline in a large cohort of young cystic fibrosis patients.Semantic proximity Read ↗

Quantification of Phenotypic Variability of Lung Disease in Children with Cystic Fibrosis.Semantic proximity Read ↗

Introduction to section I: overview of approaches to study cystic fibrosis pathophysiology.Semantic proximity Read ↗

Phenotypes of Rapid Cystic Fibrosis Lung Disease Progression during Adolescence and Young Adulthood.Semantic proximity Read ↗

Influence of pancreatic status, CFTR mutations, Staphylococcus aureus and/or Pseudomonas aeruginosa infection/colonization on lung function in cystic fibrosis during a 2-year follow-up period.Semantic proximity Read ↗

Factors associated with within-individual variability of lung function for people with cystic fibrosis: a longitudinal registry studySemantic proximity Read ↗

Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients.Semantic proximity Read ↗

Lung clearance index to characterize clinical phenotypes of children and adolescents with cystic fibrosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.