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

Authors
Category Primary study
JournalFront. Endocrinol.
Year 2026
This article has no abstract
Epistemonikos ID: 3d9da9ad75247792b02e36077707064f6fd47b0b
First added on: Oct 10, 2026