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Evgenia Globa
Evgenia Globa
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Year
Both low blood glucose and insufficient treatment confer risk of neurodevelopmental impairment in congenital hyperinsulinism: a multinational cohort study
A Helleskov, M Melikyan, E Globa, I Shcherderkina, F Poertner, ...
Frontiers in endocrinology 8, 156, 2017
682017
Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46, XY gonadal dysgenesis and 46, XY testicular regression syndrome
K McElreavey, A Jorgensen, C Eozenou, T Merel, J Bignon-Topalovic, ...
Genetics in Medicine 22 (1), 150-159, 2020
592020
International comparison of glycaemic control in people with type 1 diabetes: an update and extension
R Prigge, JA McKnight, SH Wild, A Haynes, TW Jones, EA Davis, ...
Diabetic Medicine 39 (5), e14766, 2022
422022
18F-DOPA PET/CT and 68Ga-DOTANOC PET/CT scans as diagnostic tools in focal congenital hyperinsulinism: a blinded evaluation
CD Christiansen, H Petersen, AL Nielsen, S Detlefsen, K Brusgaard, ...
European Journal of Nuclear Medicine and Molecular Imaging 45, 250-261, 2018
422018
Neonatal diabetes in Ukraine: incidence, genetics, clinical phenotype and treatment
E Globa, N Zelinska, DJG Mackay, KI Temple, JAL Houghton, ...
Journal of Pediatric Endocrinology and Metabolism 28 (11-12), 1279-1286, 2015
402015
Nationwide study of Turner syndrome in Ukrainian children: prevalence, genetic variants and phenotypic features
N Zelinska, I Shevchenko, E Globa
Journal of clinical research in pediatric endocrinology 10 (3), 256, 2018
252018
Disorders of sex development in a large Ukrainian cohort: clinical diversity and genetic findings
E Globa, N Zelinska, Y Shcherbak, J Bignon-Topalovic, A Bashamboo, ...
Frontiers in endocrinology 13, 810782, 2022
232022
The difficult management of persistent, non‐focal congenital hyperinsulinism: A retrospective review from a single, tertiary center
AG Rasmussen, M Melikian, E Globa, S Detlefsen, L Rasmussen, ...
Pediatric Diabetes 21 (3), 441-455, 2020
142020
Intraoperative ultrasound: a tool to support tissue-sparing curative pancreatic resection in focal congenital hyperinsulinism
J Bendix, MG Laursen, MB Mortensen, M Melikian, E Globa, S Detlefsen, ...
Frontiers in endocrinology 9, 478, 2018
122018
The clinical cases of Geleophysic dysplasia: one gene, different phenotypes
E Globa, N Zelinska, A Dauber
Case Reports in Endocrinology 2018, 2018
122018
Identification of GCK‐maturity‐onset diabetes of the young in cases of neonatal hyperglycemia: A case series and review of clinical features
AE Hughes, E De Franco, E Globa, N Zelinska, D Hilgard, P Sifianou, ...
Pediatric diabetes 22 (6), 876-881, 2021
102021
MODY in Ukraine: genes, clinical phenotypes and treatment
E Globa, N Zelinska, L Elblova, P Dusatkova, O Cinek, J Lebl, ...
Journal of Pediatric Endocrinology and Metabolism 30 (10), 1095-1103, 2017
102017
Gonadectomy in conditions affecting sex development: a registry-based cohort study
AK Lucas-Herald, J Bryce, A Kyriakou, ML Ljubicic, W Arlt, L Audi, ...
European journal of endocrinology 184 (6), 791-801, 2021
92021
Diseases of the endocrine system in children in Ukraine and the provision of specialized care to pediatric patients in 2020
NB Zelinska, NG Rudenko, EV Globa, OV Rudenko, К Grishchenko, ...
Ukrainian Journal of Pediatric Endocrinology,(2), 4-14, 2021
62021
Intraoperative ultrasound imaging in the surgical treatment of congenital hyperinsulinism: prospective, blinded study
AP Bjarnesen, P Dahlin, E Globa, H Petersen, K Brusgaard, L Rasmussen, ...
BJS open 5 (2), zraa008, 2021
52021
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development
C Kouri, G Sommer, IM de Lapiscina, RN Elzenaty, LJW Tack, M Cools, ...
EBioMedicine 99, 2024
42024
Testosterone therapy and its monitoring in adolescent boys with hypogonadism: results of an international survey from the I-DSD registry
MR Stancampiano, AK Lucas-Herald, J Bryce, G Russo, G Barera, ...
Sexual development 15 (4), 236-243, 2021
42021
Genetic testing of DSD patients in Ukraine
Y Shcherbak, N Zelinska, I Schevchenko, E Globa, A Bashamboo, ...
Abstracts for 58th Annual Meeting of the European Society for Paediatric …, 2019
42019
Mutations in CBX2 associated with gonadal anomalies in 46, XY and 46, XX individuals
T Merel, C Eozenou, L Van Maldergem, E Globa, K McElreavey, ...
HORMONE RESEARCH IN PAEDIATRICS 91, 190-190, 2019
32019
Синдром персистенції мюллерових каналів: огляд літератури та власні дані
ЄВ Глоба, НБ Зелінська, ІЮ Шевченко, НГ Сірик
Клінічна ендокринологія та ендокринна хірургія, 77-82, 2019
32019
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