Standards for the care of people with cystic fibrosis (CF): A timely and accurate diagnosis
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference44 articles.
1. ECFS best practice guidelines: the 2018 revision;Castellani;J Cyst Fibros,2018
2. European Cystic Fibrosis Society Standards of Care: Best Practice guidelines;Smyth;J Cyst Fibros,2014
3. European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance;Munck;J Cyst Fibros,2022
4. Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID);Barben;J Cyst Fibros,2021
5. Accurate assignment of disease liability to genetic variants using only population data;Collaco;Genet Med,2022
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1. Reported Adverse Events in a Multicenter Cohort of Patients Ages 6-18 Years with Cystic Fibrosis and at Least One F508del Allele Receiving Elexacaftor/Tezacaftor/Ivacaftor;The Journal of Pediatrics;2024-11
2. Single-Cell RNA Sequencing Shows that Circulating Monocytes Enriched in IFN Signaling Are Associated with Nontuberculous Mycobacteria Pulmonary Disease in Cystic Fibrosis;American Journal of Respiratory and Critical Care Medicine;2024-09-15
3. Relationship Between Lung Volumes and Heterogeneity in the Response to Elexacaftor/Tezacaftor/Ivacaftor in Patients With Cystic Fibrosis and Advanced Lung Disease;CHEST;2024-09
4. Literary evidence of the impact of nonbiological risk factors on CRMS/CFSPID: A scoping review;Pediatric Pulmonology;2024-08-21
5. Cystic fibrosis;Nature Reviews Disease Primers;2024-08-08
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