Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort study-Reference-Cited by-同舟云学术

Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort study

Published:2019-01-22 Issue:5 Volume:54 Page:581-586
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol

Author:

Goetz Danielle¹^ORCID,Kopp Benjamin T.²^ORCID,Salvator Ann³,Moore‐Clingenpeel Melissa³,McCoy Karen²,Leung Daniel H.⁴,Kloster Margaret⁵⁶,Ramsey Bonnie R.⁵⁶,Heltshe Sonya H.⁵⁶,Borowitz Drucy¹⁷

Affiliation:

1. Department of Pediatrics, Division of Pediatric PulmonologyUniversity at BuffaloBuffaloNew York

2. Nationwide Children's HospitalDivision of Pulmonary MedicineColumbusOhio

3. Biostatistics CoreResearch Institute at Nationwide Children's HospitalColumbusOhio

4. Baylor College of Medicine, Department of PediatricsDivision of Gastroenterology, Hepatology, and NutritionHoustonTexas

5. Cystic Fibrosis Foundation Therapeutics Development Network Coordinating CenterSeattle Children's Research InstituteSeattleWashington

6. Department of Pediatrics, Division of Pulmonary and Sleep MedicineUniversity of WashingtonSeattleWashington

7. Cystic Fibrosis FoundationBethesdaMaryland

Funder

Cystic Fibrosis Foundation

National Institutes of Health

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.24261

Reference20 articles.

1. Early Diagnosis of Cystic Fibrosis Through Neonatal Screening Prevents Severe Malnutrition and Improves Long-Term Growth

2. Effects of Diagnosis by Newborn Screening for Cystic Fibrosis on Weight and Length in the First Year of Life

3. Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?

4. Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis

5. Pancreatic Enzyme Replacement Therapy Use in Infants With Cystic Fibrosis Diagnosed by Newborn Screening

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2. Developing a nutrition screening tool for children with cystic fibrosis ages 0 to 2 years;Journal of Cystic Fibrosis;2023-11

3. Disparities in first evaluation of infants with cystic fibrosis since implementation of newborn screening;Journal of Cystic Fibrosis;2023-01

4. Association between stool consistency and clinical variables among infants with cystic fibrosis: Findings from the BONUS study;Journal of Cystic Fibrosis;2022-09

5. Gastrointestinal Factors Associated With Hospitalization in Infants With Cystic Fibrosis: Results From the Baby Observational and Nutrition Study;Journal of Pediatric Gastroenterology & Nutrition;2021-05-18