Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study (Q28388812)

7

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Margaret Whitehead

2

object named as

Margaret Whitehead

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author name string

David Taylor-Robinson

1

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Hanne Vebert Olesen

4

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Tania Pressler

5

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Rosalind L Smyth

Effect of occupational exposures on decline of lung function in early chronic obstructive pulmonary disease

6

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language of work or name

English

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publication date

October 2012

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published in

Thorax

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volume

67

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page(s)

860-6

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issue

10

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cites work

1 reference

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Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Pulmonary Disease

20 March 2017

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The precision of longitudinal lung function measurements: monitoring and interpretation

20 March 2017

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Spirometric reference values from a sample of the general U.S. population

20 March 2017

1 reference

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Random-effects models for longitudinal data

20 March 2017

1 reference

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Standardisation of spirometry

20 March 2017

1 reference

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Genetic variation in TIMP1 but not MMPs predict excess FEV1 decline in two general population-based cohorts

7 April 2017

1 reference

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Improved survival at low lung function in cystic fibrosis: cohort study from 1990 to 2007.

29 September 2017

1 reference

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Pulmonary outcome prediction (POP) tools for cystic fibrosis patients.

29 September 2017

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Characterizing aggressiveness and predicting future progression of CF lung disease

29 September 2017

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Monitoring respiratory disease severity in cystic fibrosis

29 September 2017

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Longitudinal decline in lung volume in a population of children with sickle cell disease.

29 September 2017

1 reference

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Clinical use of Ibuprofen is associated with slower FEV1 decline in children with cystic fibrosis

29 September 2017

1 reference

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Poor airway function in early infancy and lung function by age 22 years: a non-selective longitudinal cohort study

29 September 2017

1 reference

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Power considerations for studies of lung function in cystic fibrosis

29 September 2017

1 reference

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Repeatability of Spirometry in 18,000 Adult Patients

29 September 2017

1 reference

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Cystic fibrosis: current survival and population estimates to the year 2000.

29 September 2017

1 reference

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Variability of routine pulmonary function tests

29 September 2017

1 reference

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Priorities for respiratory research in the UK.

29 September 2017

1 reference

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Improved survival in the Danish center-treated cystic fibrosis patients: results of aggressive treatment.

2 June 2018

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The natural history of chronic airflow obstruction revisited: an analysis of the Framingham offspring cohort

2 June 2018

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Annual assessment spirometry, plethysmography, and gas transfer in cystic fibrosis: do they predict death or transplantation.

27 November 2018

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Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis.

27 November 2018

1 reference

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Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study. Epidemiologic Registry of Cystic Fibrosis.

27 November 2018

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Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis

27 November 2018

1 reference

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Efficacy of aerosolized tobramycin in patients with cystic fibrosis.

27 November 2018

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Pulmonary function between 6 and 18 years of age.

27 November 2018

1 reference

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The repeatability of forced expiratory volume measurements in adults with cystic fibrosis

27 November 2018

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12 December 2020

Changes in measured spirometric indices. What is significant?

1 reference

12 December 2020

Variability of pulmonary function tests in cystic fibrosis

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12 December 2020

Prediction of Mortality in Patients with Cystic Fibrosis

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12 December 2020

Long-term effect of inhaled budesonide in mild and moderate chronic obstructive pulmonary disease: a randomised controlled trial

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12 December 2020

10.1136/THORAXJNL-2011-200953

Identifiers

DOI

1 reference

release_glyzrxlcezbgfikdi6oebohza4

455126

Fatcat ID

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455126

1 reference

1 reference

1 reference