Changes in fecal elastase-1 following initiation of CFTR modulator therapy in pediatric patients with cystic fibrosis-Reference-Cited by-同舟云学术

Changes in fecal elastase-1 following initiation of CFTR modulator therapy in pediatric patients with cystic fibrosis

Published:2023-11 Issue:6 Volume:22 Page:996-1001
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Stephenson Kimberly G.^ORCID,Lingle Abby J.,Baumberger Kelly A.,Dellon Elisabeth P.,Esther Charles R.,Meier Ellen M.,Oermann Christopher M.^ORCID,Shenoy Vivek K.^ORCID,Smith Natalie R.^ORCID,Wimmer Nicole S.^ORCID,Duehlmeyer Stephanie R.,Kam Charissa W.^ORCID,McKinzie Cameron J.^ORCID,Poisson Margaret O.^ORCID,Elson E. Claire^ORCID

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference20 articles.

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3. Safety, pharmacokinetics, and pharmacodynamics of ivacaftor in patients aged 2-5 years with cystic fibrosis and a CFTR gating mutation (KIWI): an open-label, single-arm study;Davies;Lancet Respir Med,2016

4. An open-label extension study of ivacaftor in children with CF and a CFTR gating mutation initiating treatment at age 2-5 years (KLIMB);Rosenfeld;J Cyst Fibrosis: Off J Eur Cyst Fibrosis Soc,2019

5. Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study;Rosenfeld;Lancet Respir Med,2018

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1. A review of proton pump inhibitor use in cystic fibrosis and considerations for deprescribing;Pediatric Pulmonology;2024-08-28

2. Clinical evidence of pancreatic recovery in children with cystic fibrosis on ivacaftor;Pediatric Pulmonology;2024-05-09

3. Highly effective cystic fibrosis transmembrane conductance (regulator) modulator therapy: shifting the curve for most while leaving some further behind;Current Opinion in Pediatrics;2024-02-15