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pro vyhledávání: '"Dana Maajali"'
Publikováno v:
Endocrines, Vol 3, Iss 1, Pp 115-126 (2022)
Congenital or monogenic hyperinsulinism (HI) is a group of rare genetic disorders characterized by dysregulated insulin secretion and is the most common cause of persistent hypoglycemia in children. Knowledge of normal glucose homeostasis allows for
Externí odkaz:
https://doaj.org/article/93ca5ae88a3943bd80627cd2285a2ed3