(Q34449048)

2 August 2017

title

Lung function decline from adolescence to young adulthood in cystic fibrosis (English)

1 reference

2 August 2017

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David J Pasta

4

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author name string

Stacy L Vandenbranden

1

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2 August 2017

Ann McMullen

2

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2 August 2017

Michael S Schechter

3

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2 August 2017

Rory L Michaelis

5

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2 August 2017

Michael W Konstan

6

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2 August 2017

Jeffrey S Wagener

7

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2 August 2017

Wayne J Morgan

8

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2 August 2017

Susanna A McColley

9

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2 August 2017

Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis

10

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2 August 2017

publication date

24 August 2011

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2 August 2017

published in

Pediatric Pulmonology

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2 August 2017

volume

47

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2 August 2017

issue

2

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2 August 2017

page(s)

135-143

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Clinical use of dornase alpha is associated with a slower rate of FEV1 decline in cystic fibrosis.

2 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

Year-to-year changes in lung function in individuals with cystic fibrosis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

Cystic fibrosis-related diabetes: current trends in prevalence, incidence, and mortality

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

TREATMENT OUTCOME OF TUBERCULOSIS UNDER DIRECTLY OBSERVED TREATMENT SHORT COURSE ( DOTS ) IN PATIENTS PRESENTING AT CHEST & TB HOSPITAL, AMRITSAR

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

Wasting as an independent predictor of mortality in patients with cystic fibrosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

Predictive 5-year survivorship model of cystic fibrosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

Risky behavior in teens with cystic fibrosis or sickle cell disease: a multicenter study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

Gender gap in cystic fibrosis mortality

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4219484

Relationship between inhaled corticosteroid therapy and rate of lung function decline in children with cystic fibrosis

6 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FPPUL.21526

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPPUL.21526

The self-image of adolescents with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPPUL.21526

Haemophilus influenzae forms biofilms on airway epithelia: implications in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPPUL.21526

Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPPUL.21526

Factors influencing outcomes in cystic fibrosis: a center-based analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPPUL.21526

Predictors of mortality in adults with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPPUL.21526

Transition and transfer of patients who have cystic fibrosis to adult care

21 January 2018

1 reference

12 December 2020

Changes in spirometry during consecutive admissions for infective pulmonary exacerbations in adolescent and adult cystic fibrosis

1 reference

12 December 2020

Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis

1 reference

12 December 2020

Epidemiologic study of cystic fibrosis: design and implementation of a prospective, multicenter, observational study of patients with cystic fibrosis in the U.S. and Canada

1 reference

12 December 2020

Patterns of medical practice in cystic fibrosis: part II. Use of therapies. Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis

1 reference

12 December 2020

Identifiers

DOI

10.1002/PPUL.21526

1 reference

2 August 2017

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2 August 2017

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