Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience
Author:
Funder
wellcome trust
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/s00592-021-01788-6.pdf
Reference29 articles.
1. Rabbone I, Barbetti F, Gentilella R et al (2017) Insulin therapy in neonatal diabetes mellitus: a review of the literature. Diabetes Res Clin Pract 129:126–135
2. Hattersley AT, Greeley S, Polak M et al (2018) ISPAD clinical practice consensus guidelines 2018: the diagnosis and management of monogenic diabetes in children and adolescents. Pediatr Diabetes 19(Suppl 27):47–63
3. Beltrand J, Busiah K, Vaivre-Douret L et al (2020) Neonatal diabetes mellitus. Front Paediatr 8:540718
4. Busiah, K., Drunat, S., Vaivre-Douret, L., et al. French NDM study group (2013). Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected]. The lancet. Diabetes & endocrinology, 1(3), 199–207
5. Bowman, P., Mathews, F., Barbetti, F., et al. & Neonatal Diabetes International Collaborative Group (2021). Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes. Diabetes care, 44(1), 35–42
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