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Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutationSophia Kitsiou‐Tzeli, Emmanuel Kanavakis, Sophia Malaktari-Skarantavou et al.|HORMONES|2012Cited by 9
Genetics of 21-OH Deficiency and Genotype–Phenotype Correlation: Experience of the Hellenic National Referral CenterIrene Fylaktou, Amalia Sertedaki, Anny Mertzanian et al.|Current Issues in Molecular Biology|2024Cited by 2
Whole Exome Sequencing (WES) Reveals Oligogenic Gene Mutations in a Case of Combined Pituitary Hormone Deficiency (CPHD)Amalia Sertedaki, Christina Kanaka‐Gantenbein, Elizabeth‐Barbara Tatsi et al.|58th Annual ESPE Meeting (ESPE 2019)|2019Cited by 0
Congenital Adrenal Hyperplasia caused by compound heterozygosity of two novel CYP11B1gene variants.Irene Fylaktou, Christina Kanaka‐Gantenbein, Penelope Smyrnaki et al.|59th ESPE Annual Meeting (ESPE 2021 Online)|2021Cited by 0