Osteoporosis Syndrome in Thalassaemia Major: An Overview

por Toumba, Meropi, Skordis, Nicos
Publicado 2010

Microcalcifications without a thyroid nodule as the sole sign of papillary thyroid carcinoma

por Ioakim, Stamatina, Constantinides, Vasilis, Toumba, Meropi, Lyssiotis, Theodoros, Kyriacou, Angelos
Publicado 2021

The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes

por Fanis, Pavlos, Skordis, Nicos, Toumba, Meropi, Picolos, Michalis, Tanteles, George A., Neocleous, Vassos, Phylactou, Leonidas A.
Publicado 2023

Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5′-UTR Region of the Imprinted MKRN3 Gene

por Fanis, Pavlos, Skordis, Nicos, Toumba, Meropi, Papaioannou, Nikoletta, Makris, Anestis, Kyriakou, Andreas, Neocleous, Vassos, Phylactou, Leonidas A.
Publicado 2019

Molecular modelling of novel ADCY3 variant predicts a molecular target for tackling obesity

por Toumba, Meropi, Fanis, Pavlos, Vlachakis, Dimitrios, Neocleous, Vassos, Phylactou, Leonidas A., Skordis, Nicos, Mantzoros, Christos S., Pantelidou, Maria
Publicado 2022

Methylation status of hypothalamic Mkrn3 promoter across puberty

por Fanis, Pavlos, Morrou, Maria, Tomazou, Marios, Michailidou, Kyriaki, Spyrou, George M., Toumba, Meropi, Skordis, Nicos, Neocleous, Vassos, Phylactou, Leonidas A.
Publicado 2023

Reduced serum concentrations of biomarkers reflecting Leydig and Sertoli cell function in male patients with congenital adrenal hyperplasia

por Johannsen, Trine Holm, Albrethsen, Jakob, Neocleous, Vassos, Baronio, Federico, Cools, Martine, Aksglaede, Lise, Jørgensen, Niels, Christiansen, Peter, Toumba, Meropi, Fanis, Pavlos, Ljubicic, Marie Lindhardt, Juul, Anders
Publicado 2023

Variations in the 3′UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia

por Neocleous, Vassos, Fanis, Pavlos, Toumba, Meropi, Phedonos, Alexia A. P., Picolos, Michalis, Andreou, Elena, Kyriakides, Tassos C., Tanteles, George A., Shammas, Christos, Phylactou, Leonidas A., Skordis, Nicos
Publicado 2017

GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of...

por Neocleous, Vassos, Fanis, Pavlos, Toumba, Meropi, Tanteles, George A., Schiza, Melpo, Cinarli, Feride, Nicolaides, Nicolas C., Oulas, Anastasis, Spyrou, George M., Mantzoros, Christos S., Vlachakis, Dimitrios, Skordis, Nicos, Phylactou, Leonidas A.
Publicado 2020

Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty

por Neocleous, Vassos, Fanis, Pavlos, Toumba, Meropi, Gorka, Barbara, Kousiappa, Ioanna, Tanteles, George A., Iasonides, Michalis, Nicolaides, Nicolas C., Christou, Yiolanda P., Michailidou, Kyriaki, Nicolaou, Stella, Papacostas, Savvas S., Christoforidis, Athanasios, Kyriakou, Andreas, Vlachakis, Dimitrios, Skordis, Nicos, Phylactou, Leonidas A.
Publicado 2021