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Author

Ertan Mayatepek

2 papers indexed here

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Case report Open access Aug 2026

Case Report: Pasireotide treatment in neonatal congenital hyperinsulinism due to a homozygous ABCC8 mutation

Mutations in ABCC8 and KCNJ11 are associated with the most severe and diazoxide-resistant forms of congenital hyperinsulinism (CHI). Somatostatin analogues are commonly used off-label as second-line treatment. While octreotide and lanreotide are the most established options, pasireotide—a second-generation somatostatin...

Calvin Kurz, Marcia Roeper, L. Friesl et al. · 1 citation
Open access Sep 2026

Immunophenotypic insights into diabetes heterogeneity: The role of CD25-expressing T cells in Ghanaian type 1 diabetes cohorts

Type 1 diabetes (T1D) in sub-Saharan Africa exhibits heterogeneity, characterised by alternative phenotypes that retain C-peptide levels. The T-cell pathology linked to these atypical phenotypes remains largely unexplored. CD25, the interleukin-2 receptor alpha chain, and IL2RA genetic variants are key T-cell factors i...

Wilfred Aniagyei, Sophie L. Womelsdorf, Sarah Bittner et al. · 0 citations

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