Annals of Pediatric Endocrinology & Metabolism


Genotype - phenotype correlation in an adolescent girl with pathogenic PPARy genetic variation that caused severe hypertriglyceridemia and early onset type 2 diabetes: Ana Gutierrez Alvarez, Naomi Yachelevich, Brenda Kohn, Preneet Cheema Brar; Ann Pediatr Endocrinol Metab. 2021;26(4):284-289. Published online October 14, 2021; DOI: https://doi.org/10.6065/apem.2142056.028
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Pasireotide treatment for severe congenital hyperinsulinism due to a homozygous ABCC8 mutation: Christiaan F. Mooij, Carline E. Tacke, Mirjam E. van Albada, Winfried Barthlen, Hennie Bikker, Klaus Mohnike, Matthijs W.N. Oomen, A.S. Paul van Trotsenburg, Nitash Zwaveling-Soonawala; Ann Pediatr Endocrinol Metab. 2021;26(4):278-283. Published online May 7, 2021; DOI: https://doi.org/10.6065/apem.2142010.005
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Clinical Outcome after Pancreatectomy in Patients with Persistent Hyperinsulinemic Hypoglycemia of Infancy.: Min Ho Jung, Jin Soon Hwang, Choong Ho Shin, Sei Won Yang, Je G Chi; Ann Pediatr Endocrinol Metab. 2000;5(2):171-181.; PDF

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