(Q37417046)

English

Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis

scientific article published on February 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

cystic fibrosis

0 references

0 references

1 reference

based on heuristic

inferred from title

author name string

Huichuan J Lai

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Suzanne M Shoff

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Philip M Farrell

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Wisconsin Cystic Fibrosis Neonatal Screening Group

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

1 February 2009

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

123

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

714-722

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Association of nutritional status and pulmonary function in children with cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

Antibody response to Pseudomonas aeruginosa in cystic fibrosis patients: a marker of therapeutic success?--A 30-year cohort study of survival in Danish CF patients after onset of chronic P. aeruginosa lung infection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein and amino acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

Delayed diagnosis of US females with cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

2000 CDC Growth Charts for the United States: methods and development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

Growth status in children with cystic fibrosis based on the National Cystic Fibrosis Patient Registry data: evaluation of various criteria used to identify malnutrition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

Acquisition of Pseudomonas aeruginosa in children with cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

A prospective randomized trial of early diagnosis and treatment of cystic fibrosis: a unique ethical dilemma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

Relative underweight in cystic fibrosis and its prognostic value

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

6 September 2017

Pseudomonas aeruginosa, mucoidy and the chronic infection phenotype in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

28 September 2017

Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

26 June 2018

Studies in cystic fibrosis. Report of 130 patients diagnosed under 3 months of age over a 20-year period

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

26 June 2018

Fatty acid abnormalities in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

26 June 2018

Pancreatic insufficiency, growth, and nutrition in infants identified by newborn screening as having cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

26 June 2018

The chest roentgenogram in cystic fibrosis: a new scoring system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

26 June 2018

Temporal associations among energy intake, plasma linoleic acid, and growth improvement in response to treatment initiation after diagnosis of cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: enough is enough!

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Reduction in prevalence of chronic Pseudomonas aeruginosa infection at a regional pediatric cystic fibrosis center

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Bronchopulmonary disease in children with cystic fibrosis after early or delayed diagnosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Respiratory infections with Pseudomonas aeruginosa in children with cystic fibrosis: early detection by serology and assessment of risk factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Wisconsin cystic fibrosis chest radiograph scoring system: validation and standardization for application to longitudinal studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Effect of linoleic acid intake on growth of infants with cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Pulmonary function between 6 and 18 years of age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Wisconsin cystic fibrosis chest radiograph scoring system.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775492

2 September 2018

Nutritional status of patients with cystic fibrosis with meconium ileus: a comparison with patients without meconium ileus and diagnosed early through neonatal screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of formulas for calculating total energy requirements of preadolescent children with cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stature as a prognostic factor in cystic fibrosis survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correction of linoleic acid deficiency in cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nutritional status of infants with cystic fibrosis associated with early diagnosis and intervention

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth evaluation at one year of life in infants with cystic fibrosis diagnosed by neonatal screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth dynamics in cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nutritional benefits of neonatal screening for cystic fibrosis. Wisconsin Cystic Fibrosis Neonatal Screening Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure to thrive: the earliest feature of cystic fibrosis in infants diagnosed by neonatal screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth failure in cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term study of one hundred five patients with cystic fibrosis; studies made over a five- to fourteen-year period

1 reference

https://pubmed.ncbi.nlm.nih.gov/19171643

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1542/PEDS.2007-3089

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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