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

Calvin Kurz, Marcia Roeper, Lisa Friesl, Ertan Mayatepek, Thomas Meissner, Sebastian Kummer, Henrike Hoermann, Alena Welters

Open source

DOI: 10.3389/fendo.2026.1873953
Published: 2026-08-27
Container: Frontiers in Endocrinology
Publisher: Frontiers Media SA
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3389/fendo.2026.1873953,
  title = {Case Report: Pasireotide treatment in neonatal congenital hyperinsulinism due to a homozygous ABCC8 mutation},
  author = {Calvin Kurz and Marcia Roeper and Lisa Friesl and Ertan Mayatepek and Thomas Meissner and Sebastian Kummer and Henrike Hoermann and Alena Welters},
  year = {2026},
  journal = {Frontiers in Endocrinology},
  doi = {10.3389/fendo.2026.1873953},
  url = {https://doi.org/10.3389/fendo.2026.1873953}
}

RIS

TY  - JOUR
TI  - Case Report: Pasireotide treatment in neonatal congenital hyperinsulinism due to a homozygous ABCC8 mutation
AU  - Calvin Kurz
AU  - Marcia Roeper
AU  - Lisa Friesl
AU  - Ertan Mayatepek
AU  - Thomas Meissner
AU  - Sebastian Kummer
AU  - Henrike Hoermann
AU  - Alena Welters
PY  - 2026
JO  - Frontiers in Endocrinology
DO  - 10.3389/fendo.2026.1873953
UR  - https://doi.org/10.3389/fendo.2026.1873953
ER  -

APA

Kurz, C., Roeper, M., Friesl, L., Mayatepek, E., Meissner, T., Kummer, S., Hoermann, H., & Welters, A. (2026). Case Report: Pasireotide treatment in neonatal congenital hyperinsulinism due to a homozygous ABCC8 mutation. Frontiers in Endocrinology. https://doi.org/10.3389/fendo.2026.1873953

Source records

crossref · retrieved 2026-09-25T20:09:47.605Z