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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
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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
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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.
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