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

    Article • Journal of Pediatric Endocrinology and Metabolism, October 2020, De Gruyter

    ELPIS ATHINA VLACHOPAPADOPOULOU

  2. Pseudohypoparathyroidism type 1B (PHP1B), a rare disorder encountered in adolescence

    Article • Journal of Pediatric Endocrinology and Metabolism, October 2020, De Gruyter

    ELPIS ATHINA VLACHOPAPADOPOULOU

  3. A Randomized Phase 2 Study of Long-Acting TransCon GH vs Daily GH in Childhood GH Deficiency

    Article • The Journal of Clinical Endocrinology & Metabolism, February 2017, Endocrine Society

    ELPIS ATHINA VLACHOPAPADOPOULOU, Oleg Malievsky