Continuous glucose monitoring in cystic fibrosis–Benefits, limitations, and opportunities
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference13 articles.
1. Clinical care guidelines for cystic fibrosis-related diabetes–A position statement of the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society;Moran;Diabetes Care,2010
2. Continuous glucose monitoring abnormalities in cystic fibrosis youth correlate with pulmonary function decline;Chan;J Cyst Fibros,2018
3. Continuous glucose monitoring in cystic fibrosis–A practical guide;Chan;J Cyst Fibros,2019
4. Predictors for future cystic fibrosis-related diabetes by oral glucose tolerance test;Schmid;J Cyst Fibros,2014
5. Trends in pulmonary function in patients with cystic fibrosis correlate with the degree of glucose intolerance at baseline;Milla;Am J Respir Crit Care Med,2000
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1. Early glucose abnormalities revealed by continuous glucose monitoring associate with lung function decline in cystic fibrosis: A five-year prospective study;Journal of Diabetes and its Complications;2024-04
2. An Update in Cystic Fibrosis-Related Diabetes in Children and Adolescents;Children;2023-11-30
3. Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis;Journal of Cystic Fibrosis;2023-01
4. Comparison of continuous glucose monitoring to reference standard oral glucose tolerance test for the detection of dysglycemia in cystic Fibrosis: A systematic review;Journal of Clinical & Translational Endocrinology;2022-12
5. Clinical practice versus guidelines for the screening of cystic fibrosis-related diabetes: A French survey from the 47 centers;Journal of Clinical & Translational Endocrinology;2022-06
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