Defining and identifying early‐onset lung disease in cystic fibrosis with cumulative clinical characteristics-Reference-Cited by-同舟云学术

Defining and identifying early‐onset lung disease in cystic fibrosis with cumulative clinical characteristics

Published:2022-06-25 Issue:10 Volume:57 Page:2363-2373
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatric Pulmonology

Author:

Huang Leslie¹^ORCID,Lai HuiChuan J.¹²³^ORCID,Antos Nicholas⁴^ORCID,Rock Michael J.¹^ORCID,Asfour Fadi⁵,Howenstine Michelle⁶,Gaffin Jonathan M.⁷^ORCID,Farrell Philip M.¹³^ORCID

Affiliation:

1. Department of Pediatrics University of Wisconsin—Madison Madison Wisconsin USA

2. Department of Nutritional Sciences University of Wisconsin—Madison Madison Wisconsin USA

3. Department of Population Health Sciences University of Wisconsin—Madison Madison Wisconsin USA

4. Department of Pediatrics Medical College of Wisconsin Milwaukee Wisconsin USA

5. Department of Pediatrics University of Utah Salt Lake City Utah USA

6. Department of Pediatrics Indiana University Indianapolis Indiana USA

7. Department of Pediatrics Boston Children's Hospital Boston Massachusetts USA

Funder

Cystic Fibrosis Foundation

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.26040

Reference34 articles.

1. Newborn Screening for CF across the Globe—Where Is It Worthwhile?

2. Differences in clinical outcomes of paediatric cystic fibrosis patients with and without meconium ileus

3. Cystic fibrosis foundation evidence‐based guidelines for management of infants with cystic fibrosis;Cystic Fibrosis F;J Pediatr,2009

4. Outcomes of infants born during the first 9 years of CF newborn screening in the United States: A retrospective Cystic Fibrosis Foundation Patient Registry cohort study

5. Fibrocystic Disease of the Pancreas in the Newborn

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