Article
Publicly Available
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Published/Copyright:
January 8, 2026
Published Online: 2026-01-08
Published in Print: 2026-01-23
©2026 Walter de Gruyter GmbH, Berlin/Boston
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- Exploratory real-world experience with GLP-1 receptor agonists vs. metformin in youth with new-onset type 2 diabetes: a single-center retrospective study
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- Clinical insights of the TBX19 C.856 C>T variant: a case report and literature review on neonatal isolated ACTH deficiency
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Articles in the same Issue
- Frontmatter
- Review
- Prevalence of congenital hypothyroidism in infants of mothers with hypothyroidism: a meta-analysis
- Original Articles
- Pubertal characteristics, final height, and associated factors in patients with nonclassical congenital adrenal hyperplasia: a single center experience
- Serum α-Klotho and its association with testosterone in boys with central precocious puberty
- Bioelectrical impedance analysis and hormonal assessment in adolescents with pubertal gynecomastia
- The relationship between FSTL-1 (follistatin-related protein 1), FAM19A5 (family with sequence similarity 19, member A5) and CTRP-6 (C1q/TNF-related protein 6) levels and metabolic parameters in overweight children
- Role of hyperandrogenism on disordered eating behaviors in adolescents with PCOS and interplay with insulin resistance
- The impact of hepatic steatosis on epicardial adipose tissue in obese individuals
- Exploratory real-world experience with GLP-1 receptor agonists vs. metformin in youth with new-onset type 2 diabetes: a single-center retrospective study
- Characterization of monogenic diabetes among Sudanese children: a multi-center experience from a population with high consanguinity
- Short Communication
- Implementation and feasibility of a nutrition assessment for recently diagnosed youth with type 2 diabetes
- Case Reports
- Noonan syndrome and autoimmune hepatitis: patient report and literature review
- Adrenal oncocytoma: an unusual etiology of Cushing’s syndrome in an adolescent female
- Novel MCT8 mutation: diagnostic value of T3/T4 ratio
- Clinical insights of the TBX19 C.856 C>T variant: a case report and literature review on neonatal isolated ACTH deficiency
- Wolcott–Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene
