Annals of Pediatric Endocrinology & Metabolism


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
Web of Science 5 Crossref 8; Full text PubReader ePub PDF


Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8: Julie Mouron-Hryciuk, Sophie Stoppa-Vaucher, Kanetee Busiah, Thérèse Bouthors, Maria Christina Antoniou, Eric Jacot, Klaus Brusgaard, Henrik Thybo Christesen, Khalid Hussain, Andrew Dwyer, Matthias Roth-Kleiner, Michael Hauschild; Ann Pediatr Endocrinol Metab. 2021;26(1):60-65. Published online August 7, 2020; DOI: https://doi.org/10.6065/apem.2040042.021
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Congenital hyperinsulinism: diagnostic and management challenges in a developing country – case report: Cheri Mathews John, Prakash Agarwal, Suriyakumar Govindarajulu, Sandhya Sundaram, Senthil Senniappan; Ann Pediatr Endocrinol Metab. 2017;22(4):272-275. Published online December 31, 2017; DOI: https://doi.org/10.6065/apem.2017.22.4.272
Web of Science 3 Crossref 2; Full text PubReader ePub PDF


Congenital hyperinsulinism: current status and future perspectives: Tohru Yorifuji; Ann Pediatr Endocrinol Metab. 2014;19(2):57-68. Published online June 30, 2014; DOI: https://doi.org/10.6065/apem.2014.19.2.57
Crossref 55; Full text PubReader ePub PDF


A Case of Hyperinsulinism/Hyperammonemia (HI/HA) Syndrome due to a Mutation in the Glutamate Dehydrogenase Gene (GLUD1).: Hye Young Jin, Jin Ho Choi, Gu Hwan Kim, Jung Min Ko, Han Wook Yoo; Ann Pediatr Endocrinol Metab. 2009;14(2):168-173.; PDF


A Case of Hyperinsulinism/hyperammonemia Syndrome.: Ji Yeon Sung, Su Young Hong, Choong Ho Shin, Sei Won Yang; Ann Pediatr Endocrinol Metab. 2005;10(2):236-240.; PDF

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