Glycogen storage diseases
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://www.nature.com/articles/s41572-023-00456-z.pdf
Reference247 articles.
1. Ferreira, C. R., Rahman, S., Keller, M., Zschocke, J. & Group, I. A. An international classification of inherited metabolic disorders (ICIMD). J. Inherit. Metab. Dis. 44, 164–177 (2021).
2. Brown, L. M. et al. Evaluation of glycogen storage disease as a cause of ketotic hypoglycemia in children. J. Inherit. Metab. Dis. 38, 489–493 (2015).
3. Haring, M. P. D. et al. High childhood serum triglyceride concentrations associate with hepatocellular adenoma development in patients with glycogen storage disease type Ia. JHEP Rep. 4, 100512 (2022).
4. Derks, T. G. J. et al. The potential of dietary treatment in patients with glycogen storage disease type IV. J. Inherit. Metab. Dis. 44, 693–704 (2021).
5. Santalla, A. et al. Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update. BMC Genomics 18, 819 (2017).
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