Vassos Neocleous
Nicosia, 1683, Cyprus
Last Updated: 09/26/2026
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Found 56 publications
Congenital Adrenal Hyperplasia in the Mediterranean: A Concise Overview.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: April 07, 2026
Serum and serum-derived extracellular vesicle microRNA signatures linked to neurodevelopmental processes in central precocious puberty.
Journal: Frontiers in endocrinology
Published: March 13, 2026
Co-segregation of the c.489+3A>G variant with p.Cys1400Ter pathogenic CFTR mutation in Cyprus: prevalence and clinical implications.
Journal: Orphanet journal of rare diseases
Published: December 18, 2024
Identification of puberty related miRNAs in the hypothalamus of female mice.
Journal: Molecular and cellular endocrinology
Published: September 10, 2024
Genetic diagnosis of endocrine disorders in Cyprus through the Cyprus Institute of Neurology and Genetics: an ENDO-ERN Reference Center.
Journal: Orphanet journal of rare diseases
Published: November 22, 2023
Gonadotropin-Releasing Hormone Receptor (GnRHR) and Hypogonadotropic Hypogonadism.
Journal: International journal of molecular sciences
Published: October 04, 2023
Reduced serum concentrations of biomarkers reflecting Leydig and Sertoli cell function in male patients with congenital adrenal hyperplasia.
Journal: Endocrine connections
Published: April 28, 2023
RET Proto-Oncogene Variants in Patients with Medullary Thyroid Carcinoma from the Mediterranean Basin: A Brief Report.
Journal: Life (Basel, Switzerland)
Published: April 24, 2023
The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes.
Journal: Frontiers in endocrinology
Published: February 01, 2023
A novel pathogenic variant in ZNF462 gene associated with Weiss-Kruszka syndrome and systemic lupus erythematosus.
Journal: Rheumatology (Oxford, England)
Published: January 15, 2023
Methylation status of hypothalamic Mkrn3 promoter across puberty.
Journal: Frontiers in endocrinology
Published: October 20, 2022
Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene.
Journal: Hormones (Athens, Greece)
Published: April 20, 2022
Last Updated: 09/26/2026