Cystic fibrosis newborn screening does not delay the identification of cystic fibrosis in children with negative results

Author:

MacLean Joanna E.,Solomon Melinda,Corey Mary,Selvadurai Hiran

Publisher

Elsevier BV

Subject

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

Cited by 11 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. Chapter 24: Metabolic/Respiratory: Ivacaftor/CFTR Case;Pharmacogenomics: Foundations, Competencies, and the Pharmacists’ Patient Care Process, 2nd Edition;2022-08

2. Achterbahnfahrt der Elektrolyte;Pädiatrie;2021-06

3. Clinical and Genotypical Features of False-Negative Patients in 26 Years of Cystic Fibrosis Neonatal Screening in Tuscany, Italy;Diagnostics;2020-07-01

4. Chapter 23: Respiratory: Ivacaftor/CFTR Case;Pharmacogenomics: Foundations, Competencies, and the Pharmacists’ Patient Care Process;2020-01

5. S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy;Italian Journal of Pediatrics;2018-01-03

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