Early Life Height Attainment in Cystic Fibrosis Is Associated with Pulmonary Function at Age 6 Years-Reference-Cited by-同舟云学术

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Early Life Height Attainment in Cystic Fibrosis Is Associated with Pulmonary Function at Age 6 Years

Published:2021-01-21 Issue: Volume: Page:
ISSN:2329-6933
Container-title:Annals of the American Thoracic Society
language:en
Short-container-title:Annals ATS

Author:

Sanders Don B¹,Slaven James E²,Maguiness Karen³,Chmiel James F³,Ren Clement L³

Affiliation:

1. Indiana University School of Medicine, 12250, Pediatrics, Indianapolis, Indiana, United States;

2. Indiana University School of Medicine, 12250, Statistics, Indianapolis, Indiana, United States

3. Indiana University School of Medicine, 12250, Pediatrics, Indianapolis, Indiana, United States

Publisher

American Thoracic Society

Subject

Pulmonary and Respiratory Medicine

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Improving growth in infants with CF;Pediatric Pulmonology;2024-08-06

2. Diagnosis and Management of Simple and Complicated Meconium Ileus in Cystic Fibrosis, a Systematic Review;Diagnostics;2024-06-04

3. Association of in‐line digestive enzyme cartridge with enteral feeds on improvement in anthropometrics among pediatric patients with cystic fibrosis;Nutrition in Clinical Practice;2024-03-16

4. Growth in childhood chronic conditions;Reference Module in Biomedical Sciences;2024

5. Late Diagnosis in the Era of Universal Newborn Screening Negatively Affects Short- and Long-Term Growth and Health Outcomes in Infants with Cystic Fibrosis;The Journal of Pediatrics;2023-11

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