Looking for the skeleton in the closet—rare genetic diagnoses in patients with diabetes and skeletal manifestations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00592-022-01854-7.pdf
Reference45 articles.
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2. Leete P, Oram RA, McDonald TJ et al (2020) Studies of insulin and proinsulin in pancreas and serum support the existence of aetiopathological endotypes of type 1 diabetes associated with age at diagnosis. Diabetologia 63:1258–1267. https://doi.org/10.1007/s00125-020-05115-6
3. Battaglia M, Ahmed S, Anderson MS et al (2020) Introducing the endotype concept to address the challenge of disease heterogeneity in Type 1 diabetes. Diabetes Care 43:5–12. https://doi.org/10.2337/dc19-0880
4. Delvecchio M, Pastore C, Giordano P (2020) Treatment options for MODY patients: a systematic review of literature. Diabetes Ther 11:1667–1685. https://doi.org/10.1007/s13300-020-00864-4
5. Shepherd M, Shields B, Hammersley S et al (2016) Systematic population screening, using biomarkers and genetic testing, identifies 2.5% of the UK pediatric diabetes population with monogenic diabetes. Diabetes Care 39:1879–1888. https://doi.org/10.2337/dc16-0645
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