Real-world assessment of LCI following lumacaftor-ivacaftor initiation in adolescents and adults with cystic fibrosis
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference14 articles.
1. Lung clearance index: evidence for use in clinical trials in cystic fibrosis;Kent;J Cyst Fibros,2014
2. Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial;Davies;Lancet Respir Med,2013
3. Lumacaftor/ivacaftor in patients aged 6-11 years with cystic fibrosis and homozygous for F508del-CFTR;Milla;Am J Respir Crit Care Med,2017
4. Efficacy and safety of lumacaftor and ivacaftor in patients aged 6-11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial;Ratjen;Lancet Respir Med,2017
5. Changes in LCI in F508del/F508del patients treated with lumacaftor/ivacaftor: results from the prospect study;Shaw;J Cyst Fibros,2020
Cited by 6 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. The clinical impact of Lumacaftor-Ivacaftor on structural lung disease and lung function in children aged 6–11 with cystic fibrosis in a real-world setting;Respiratory Research;2023-08-11
2. Editorial: New insights into caring for pediatric patients with cystic fibrosis;Frontiers in Pediatrics;2023-08-09
3. Lung clearance index in children with cystic fibrosis previously diagnosed with CRMS/CFSPID: A monocentric prospective experience;Pediatric Pulmonology;2023-05-03
4. CFTR Modulators in People with Cystic Fibrosis: Real-World Evidence in France;Cells;2022-05-28
5. An Update on CFTR Modulators as New Therapies for Cystic Fibrosis;Pediatric Drugs;2022-05-16
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