(Q33821761)

29 July 2017

Classic respiratory disease but atypical diagnostic testing distinguishes adult presentation of cystic fibrosis (English)

1 reference

29 July 2017

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Claire L Keating

1

1 reference

29 July 2017

Xinhua Liu

series ordinal

2

1 reference

29 July 2017

Emily A Dimango

series ordinal

3

1 reference

29 July 2017

language of work or name

English

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publication date

4 December 2009

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29 July 2017

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29 July 2017

137

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29 July 2017

5

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29 July 2017

1157-1163

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Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Predictors of mucoid Pseudomonas colonization in cystic fibrosis patients

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Complex two-gene modulation of lung disease severity in children with cystic fibrosis.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Nonclassic cystic fibrosis and CFTR-related diseases

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Type I, II, III, IV, and V cystic fibrosis transmembrane conductance regulator defects and opportunities for therapy.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Gender gap in cystic fibrosis mortality

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Genetic and clinical features of patients with cystic fibrosis diagnosed after the age of 16 years

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

CFTR genotypes in patients with normal or borderline sweat chloride levels

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

End-organ dysfunction in cystic fibrosis: association with angiotensin I converting enzyme and cytokine gene polymorphisms.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Nontuberculous mycobacteria. I: multicenter prevalence study in cystic fibrosis.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

CFTR Genotype as a Predictor of Prognosis in Cystic Fibrosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862398

Late diagnosis defines a unique population of long-term survivors of cystic fibrosis

29 October 2018

1 reference

12 December 2020

Genetic modifiers of lung disease in cystic fibrosis

1 reference

12 December 2020

Cystic fibrosis mutations with widely variable phenotype: the D1152H example

1 reference

12 December 2020

Health status and sociodemographic characteristics of adults receiving a cystic fibrosis diagnosis after age 18 years

1 reference

12 December 2020

Clinical features associated with a delayed diagnosis of cystic fibrosis

1 reference

12 December 2020

Pancreatic function in infants identified as having cystic fibrosis in a neonatal screening program

1 reference

12 December 2020

Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutation

1 reference

12 December 2020

Correlation between genotype and phenotype in patients with cystic fibrosis

1 reference

12 December 2020

Delta F508 genotype does not predict disease severity in an ethnically diverse cystic fibrosis population

1 reference

12 December 2020

Identifiers

DOI

10.1378/CHEST.09-1352

1 reference

29 July 2017

1 reference

29 July 2017

1 reference