Restoration of exocrine pancreatic function in older children with cystic fibrosis on ivacaftor
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health
Reference18 articles.
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2. Davies JC on behalf of KLIMB study group. An open-label extension study of ivacaftor in children with CF and CFTR gating mutation initiating treatment at age 2–5 years (KLIMB);Rosenfeld;J Cyst Fibros,2019
3. ARRIVAL study group. 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
4. Cystic fibrosis of the pancreas and its relation to celiac disease: a clinical and pathologic study;Anderson;Am J Dis Child,1938
5. Pathophysiology of the exocrine pancreas in cystic fibrosis;Durie;J R Soc Med,1989
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