Access to Diabetes Care Should Be a Universal Right for People With Type 1 Diabetes: Lessons Learned From the Norwegian Childhood Diabetes Registry
Author:
Affiliation:
1. Department of Medicine and Pediatrics, Barbara Davis Center for Diabetes, University of Colorado, Aurora, CO
Publisher
American Diabetes Association
Link
https://diabetesjournals.org/care/article-pdf/47/7/1111/774115/dci240002.pdf
Reference15 articles.
1. Longitudinal trends in glycemic outcomes and technology use for over 48,000 people with type 1 diabetes (2016–2022) from the T1D Exchange quality improvement collaborative;Ebekozien;Diabetes Technol Ther,2023
2. Changes in HbA1c between 2011 and 2017 in Germany/Austria, Sweden, and the United States: a lifespan perspective;Albanese-O’Neill;Diabetes Technol Ther,2022
3. Temporal changes in hemoglobin A1c and diabetes technology use in DPV, NPDA, and T1DX pediatric cohorts from 2010 to 2018;Lal;Diabetes Technol Ther,2022
4. The transatlantic HbA1c gap: differences in glycaemic control across the lifespan between people included in the US T1D exchange registry and those included in the German/Austrian DPV registry;Hermann;Diabet Med,2020
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