Evgenia Globa
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Explore the profile of Evgenia Globa including associated specialties, affiliations and a list of published articles.
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26
Citations
183
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Recent Articles
1.
Boogers L, Bruggenwirth H, Wolffenbuttel K, Hersmus R, Bryce J, Ahmed S, et al.
Eur J Endocrinol
. 2025 Jan;
192(1):34-45.
PMID: 39782875
Objective: 17β-Hydroxysteroid dehydrogenase 3 deficiency (17β-HSDD) and 5α-reductase type 2 deficiency (5α-RD) are rare 46,XY differences of sex development (DSD). This study aims to enlarge the limited knowledge on long-term...
2.
Mathara Diddhenipothage S, Beck K, Amiyangoda C, Amiyangoda G, Bryce J, Cima L, et al.
Endocr Connect
. 2025 Jan;
14(2).
PMID: 39773908
Introduction: Cardiovascular disease is the most common cause of death in Turner syndrome (TS) for which arterial hypertension has a direct influence and is a key modifiable risk factor. Objective:...
3.
Globa E, Christesen H, Mortensen M, Houghton J, Nielsen A, Detlefsen S, et al.
Front Endocrinol (Lausanne)
. 2025 Jan;
15:1497579.
PMID: 39741883
Introduction: Congenital Hyperinsulinism (CHI) has not been previously studied in Ukraine. We therefore aimed to elucidate the genetics, clinical phenotype, histological subtype, treatment and long-term outcomes of Ukrainian patients with...
4.
Widening the phenotypic spectrum caused by pathogenic variants in individuals with neonatal diabetes
Jeffery N, Al Nimri O, Houghton J, Globa E, Wakeling M, Flanagan S, et al.
BMJ Open Diabetes Res Care
. 2024 Nov;
12(6).
PMID: 39542526
Introduction: Biallelic variants are a rare cause of isolated pancreatic agenesis and neonatal diabetes (NDM) without exocrine pancreatic insufficiency, with 17 cases reported in the literature. Research Design And Methods:...
5.
Tseretopoulou X, Ali S, Bryce J, Amin N, Atapattu N, Bachega T, et al.
J Endocr Soc
. 2024 Sep;
8(10):bvae145.
PMID: 39258010
Background: It is unclear whether targeted monitoring of acute adrenal insufficiency (AI) related adverse events (AE) such as sick day episodes (SDEs) and hospitalization rate in congenital adrenal hyperplasia (CAH)...
6.
Patjamontri S, Lucas-Herald A, Bryce J, van den Akker E, Cools M, Globa E, et al.
J Clin Endocrinol Metab
. 2024 Aug;
PMID: 39213311
Introduction: Partial androgen insensitivity syndrome (PAIS) is a rare condition that is reported to be commonly associated with gynecomastia in males. Objectives: To assess the management of gynecomastia in male...
7.
Badura-Stronka M, Hirschfeld A, Globa E, Winczewska-Wiktor A, Potulska-Chromik A, Kostera-Pruszczyk A, et al.
J Appl Genet
. 2024 Aug;
PMID: 39153170
We report three patients with the novel variant c.100 + 1G > A of the TBCE gene and describe the presented clinical phenotype in detail. We also systematically reviewed the...
8.
Scougall K, Bryce J, Baronio F, Boal R, Castera J, Castro S, et al.
World J Pediatr Surg
. 2023 Oct;
6(4):e000599.
PMID: 37860275
Background: Complications are frequently reported after hypospadias repair and there is a need to understand the factors that influence their occurrence. Methods: Data from boys with hypospadias born between 2000...
9.
Schroder M, Neacsu M, Adriaansen B, Sweep F, Ahmed S, Ali S, et al.
Eur J Endocrinol
. 2023 Oct;
189(4):460-468.
PMID: 37837609
Importance: Testicular adrenal rest tumors (TARTs), often found in male patients with congenital adrenal hyperplasia (CAH), are benign lesions causing testicular damage and infertility. We hypothesize that chronically elevated adrenocorticotropic...
10.
Globa E, Zelinska N, Johnson M, Flanagan S, De Franco E
Diabet Med
. 2022 Nov;
40(5):e15013.
PMID: 36398453
Aims: The aim of this study is to elucidate the aetiology and clinical features of neonatal and early-onset diabetes in a large database for pediatric diabetes patients in Ukraine. Methods:...