Glucose abnormalities detected by continuous glucose monitoring are common in young children with Cystic Fibrosis
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. Epidemiology, pathophysiology, and prognostic implications of cystic fibrosis-related diabetes: a technical review;Moran;Diabetes Care,2010
2. Influence of the development of diabetes mellitus on clinical status in patients with cystic fibrosis;Lanng;Eur J Pediatr,1992
3. Early assessment of glucose abnormalities during continuous glucose monitoring associated with lung function impairment in cystic fibrosis patients;Leclercq;J Cystic Fibrosis,2014
4. Peak OGTT glucose is associated with lower lung function in young children with cystic fibrosis;Prentice;J Cystic Fibrosis,2019
5. Abnormal glucose tolerance in infants and young children with cystic fibrosis;Yi;Am J Respir Crit Care Med,2016
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1. Advances in diabetes technology to improve the lives of people with cystic fibrosis;Diabetologia;2024-07-12
2. SHIFTing goals in cystic fibrosis—managing extrapulmonary disease in the era of CFTR modulator therapy; Proceedings of the International Shaping Initiatives and Future Trends (SHIFT) Symposium;Pediatric Pulmonology;2024-04-12
3. The Role of Continuous Glucose Monitoring in Detecting Early Dysglycemia and Clinical Outcomes in Patients with Cystic Fibrosis;Medicina;2024-03-14
4. An Update in Cystic Fibrosis-Related Diabetes in Children and Adolescents;Children;2023-11-30
5. Reproducibility of in-home CFRD screening using continuous glucose monitoring and mixed meal tolerance test;Journal of Clinical & Translational Endocrinology;2023-09
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