Use of a mobile application for self-management of pancreatic enzyme replacement therapy is associated with improved gastro-intestinal related quality of life in children with Cystic Fibrosis
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference25 articles.
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2. Contribution of pancreatic enzyme replacement therapy to survival and quality of life in patients with pancreatic exocrine insufficiency;Layer;World J Gastroenterol,2019
3. European cystic fibrosis society standards of care: best practice guidelines;Smyth;J Cyst Fibros,2014
4. ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis;Turck;Clin Nutr,2016
5. Pancreatic insufficiency in cystic fibrosis;Singh;J Cyst Fibros,2017
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4. Dynamics of abdominal symptoms during the start of a new therapy with elexacaftor/tezacaftor/ivacaftor using the novel CFAbd-day2day questionnaire;Frontiers in Pharmacology;2023-10-25
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