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Vassos Neocleous

As seen in: Frontiers, MDPI
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Articles

Gonadotropin-Releasing Hormone Receptor (GnRHR) and Hypogonadotropic Hypogonadism

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By Pavlos Fanis, Vassos Neocleous, Leonidas A. Phylactou, Irene Papapetrou
| MDPI
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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RET Proto-Oncogene Variants in Patients with Medullary Thyroid Carcinoma from the Mediterranean Basin: A Brief Report

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By Vassos Neocleous, Savvas Frangos, Nicos Skordis, Pavlos Fanis
| MDPI
Abstract : Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant (AD) condition with very high penetrance and expressivity. It is characterized into three clinical entities recognized as MEN2A, MEN2B, and familial medullary thyroid carcinoma (FMTC). In both MEN2A and MEN2B, there is a manifestation of multicentric tumor formation in the major organs such as the thyroid, parathyroid, and adrenal glands where the RET proto-oncogene is expressed.
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The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population

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By Henrik Falhammar, Sarantis Livadas, Vassos Neocleous
| Frontiers
1 Introduction Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) caused by pathological variants in the CYP21A2 gene has been classified into a) the classical form that includes the severe salt-wasting (SW) and milder simple-virilizing (SV) forms and b) the non-classical (NC) form. The range of disease manifestations, on the other hand, appears to be a spectrum with no defined boundaries (1).
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