Vassos Neocleous
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Explore the profile of Vassos Neocleous including associated specialties, affiliations and a list of published articles.
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54
Citations
446
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Recent Articles
11.
Toumba M, Fanis P, Vlachakis D, Neocleous V, Phylactou L, Skordis N, et al.
Int J Mol Med
. 2021 Nov;
49(1).
PMID: 34821371
Severe early‑onset obesity is mainly attributed to single gene variations of the hypothalamic leptin‑melanocortin system, which is critical for controlling the balance between appetite and energy expenditure. Adenylate cyclase 3...
12.
Neocleous V, Fanis P, Toumba M, Gorka B, Kousiappa I, Tanteles G, et al.
Front Endocrinol (Lausanne)
. 2021 Oct;
12:745048.
PMID: 34630334
Background: Central precocious puberty (CPP) due to premature activation of GnRH secretion results in early epiphyseal fusion and to a significant compromise in the achieved final adult height. Currently, few...
13.
Yiallouros P, Matthaiou A, Anagnostopoulou P, Kouis P, Libik M, Adamidi T, et al.
Orphanet J Rare Dis
. 2021 Oct;
16(1):409.
PMID: 34600583
Background: Specialized clinical care for cystic fibrosis (CF) in Cyprus, a small island country, has been implemented since the 1990s. However, only recently, a national CF patient registry has been...
14.
Fanis P, Neocleous V, Kosta K, Karipiadou A, Hartmann M, Wudy S, et al.
J Pediatr Endocrinol Metab
. 2020 Nov;
34(1):131-136.
PMID: 33180036
Objectives: 3β-Hydroxysteroid dehydrogenase (3β-HSD) deficiency is a rare type of congenital adrenal hyperplasia caused by recessive loss-of-function mutations in gene. Case Presentation: We report an 8.5-year-old, 46XY, Roma boy with...
15.
Neocleous V, Fanis P, Toumba M, Tanteles G, Schiza M, Cinarli F, et al.
Front Endocrinol (Lausanne)
. 2020 Sep;
11:626.
PMID: 32982993
Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic disease caused by Gonadotropin-Releasing Hormone (GnRH) deficiency. So far a limited number of variants in several genes have been associated with the...
16.
Stefani S, Kousiappa I, Nicolaou N, Papathanasiou E, Oulas A, Fanis P, et al.
Front Integr Neurosci
. 2020 Sep;
14:45.
PMID: 32973469
Objective: Transcranial magnetic stimulation (TMS), a non-invasive procedure, stimulates the cortex evaluating the central motor pathways. The response is called motor evoked potential (MEP). Polyphasia results when the response crosses...
17.
Nicolaides N, Matheou A, Vlachou F, Neocleous V, Skordis N
Acta Biomed
. 2020 Sep;
91(3):e2020085.
PMID: 32921781
Polycystic ovarian syndrome is a common endocrinologic condition diagnosed in women of childbearing age. It is primarily associated with androgen excess and ovarian dysfunction, which contribute to menstrual irregularity, oligo-anovulation,...
18.
Fanis P, Skordis N, Toumba M, Papaioannou N, Makris A, Kyriakou A, et al.
Front Endocrinol (Lausanne)
. 2019 Oct;
10:677.
PMID: 31636607
Central Precocious Puberty (CPP) is clinically defined by the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys. To date, mutations...
19.
Neocleous V, Fanis P, Toumba M, Stylianou C, Picolos M, Andreou E, et al.
Horm Metab Res
. 2019 Sep;
51(9):586-594.
PMID: 31505704
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) is caused by mutations in the gene. The study refers to CAH patients of Greek-Cypriot ancestry between years 2007 and 2018....
20.
Neocleous V, Fanis P, Cinarli F, Kokotsis V, Oulas A, Toumba M, et al.
Hormones (Athens)
. 2019 Jun;
18(3):315-320.
PMID: 31240586
Purpose: Disorders of sex development (DSD) have been linked to gene defects that lead to gonadal dysgenesis. Herein, we aimed to identify the genetic cause of gonadal dysgenesis in a...