(Q38221780)

31 August 2017

Interpretation of lung function in infants and young children with cystic fibrosis (English)

1 reference

31 August 2017

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24948040%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

author name string

Sarath Ranganathan

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24948040%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

publication date

19 June 2014

1 reference

31 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24948040%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

volume

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24948040%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24948040%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

page(s)

792-799

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24948040%20AND%20SRC:MED&resulttype=core&format=json

Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening.

9 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Air trapping and airflow obstruction in newborn cystic fibrosis piglets

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Progression of early structural lung disease in young children with cystic fibrosis assessed using CT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

ATS/ERS statement: raised volume forced expirations in infants: guidelines for current practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Relative ability of full and partial forced expiratory maneuvers to identify diminished airway function in infants with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Method for assessment of volume of trapped gas in infants during multiple-breath inert gas washout.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Infection, inflammation, and lung function decline in infants with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Early airway infection, inflammation, and lung function in cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

A realistic validation study of a new nitrogen multiple-breath washout system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung function distinguishes preschool children with CF from healthy controls in a multi-center setting

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Evidence of diminished FEV1 and FVC in 6-year-olds followed in the European Cystic Fibrosis Patient Registry, 2007-2009.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung function from infancy to preschool in a cohort of children with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Standardisation of spirometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Serial lung function and responsiveness in cystic fibrosis during early childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Effects of pseudomonas aeruginosa colonization on lung function and anthropometric variables in children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Effect of allergic bronchopulmonary aspergillosis on lung function in children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Reasons for heterogeneous change in LCI in children with cystic fibrosis after antibiotic treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

A prognostic model for the prediction of survival in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Long-term course of lung clearance index between infancy and school-age in cystic fibrosis subjects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung clearance index at 4 years predicts subsequent lung function in children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung function from infancy to school age in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung function in infants with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Ventilatory function in infants with cystic fibrosis. Physiological assessment of halation therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Gas mixing efficiency from birth to adulthood measured by multiple-breath washout

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Age and height dependence of lung clearance index and functional residual capacity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Multiple breath nitrogen washout: a feasible alternative to mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Consensus statement for inert gas washout measurement using multiple- and single- breath tests.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Exploring the relationship between forced maximal flow at functional residual capacity and parameters of forced expiration from raised lung volume in healthy infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Cystic fibrosis: the role of the small airways

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Inflammatory responses to individual microorganisms in the lungs of children with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Haemophilus infection in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

The effect of chronic infection with Aspergillus fumigatus on lung function and hospitalization in patients with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Forced expiratory flows and volumes in infants. Normative data and lung growth.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Clinically useful spirometry in preschool-aged children: evaluation of the 2007 American Thoracic Society Guidelines

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329

Lung Function in Infants with Cystic Fibrosis Diagnosed by Newborn Screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FRESP.12329