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Eirini Dikaiakou

Boston Children's Hospital

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Detection of hepatocyte nuclear factor 4A(HNF4A) gene variant as the cause for congenital hyperinsulinism leads to revision of the diagnosis of the mother.

2020 Journal of Pediatric Endocrinology and Metabolism
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Pseudohypoparathyroidism type 1B (PHP1B), a rare disorder encountered in adolescence.

2020 Journal of Pediatric Endocrinology and Metabolism
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SUN-272 Persistent Hyperinsulinemic Hypoglycemia Due to Mutation in Hepatocyte Nuclear Factor 4A

2019 Journal of the Endocrine Society
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