Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference9 articles.
1. Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth;Farrell;Pediatrics,2001
2. Newborn screening for cystic fibrosis in Wisconsin: comparison of biochemical and molecular methods;Gregg;Pediatrics,1997
3. Immunoreactive trypsinogen screening for cystic fibrosis: characterization of infants with a false-positive screening test;Rock;Pediatr Pulmonol,1989
4. Newborn screening for cystic fibrosis is complicated by age-related decline in immunoreactive trypsinogen levels;Rock;Pediatrics,1990
5. Cystic fibrosis: a worldwide analysis of CFTR mutations—correlation with incidence data and application to screening;Bobadilla;Hum Mutat,2002
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2. Immunoreactive Trypsinogen in Infants Born to Women with Cystic Fibrosis Taking Elexacaftor–Tezacaftor–Ivacaftor;International Journal of Neonatal Screening;2023-02-21
3. Newborn Screening Program for Cystic Fibrosis in Cuba: Three Years’ Experience;Journal of Inborn Errors of Metabolism and Screening;2023
4. Missed Cystic Fibrosis Newborn Screening Cases due to Immunoreactive Trypsinogen Levels below Program Cutoffs: A National Survey of Risk Factors;International Journal of Neonatal Screening;2022-10-27
5. Newborn Screening for Cystic Fibrosis: A Qualitative Study of Successes and Challenges from Universal Screening in the United States;International Journal of Neonatal Screening;2022-06-23
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