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Winfried Barthlen 1 Article
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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