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 | 68 | 2017 |
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 | 59 | 2020 |
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 | 42 | 2022 |
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 | 42 | 2018 |
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 | 40 | 2015 |
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 | 25 | 2018 |
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 | 23 | 2022 |
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 | 14 | 2020 |
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 | 12 | 2018 |
The clinical cases of Geleophysic dysplasia: one gene, different phenotypes E Globa, N Zelinska, A Dauber Case Reports in Endocrinology 2018, 2018 | 12 | 2018 |
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 | 10 | 2021 |
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 | 10 | 2017 |
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 | 9 | 2021 |
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 | 6 | 2021 |
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 | 5 | 2021 |
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 | 4 | 2024 |
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 | 4 | 2021 |
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 | 4 | 2019 |
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 | 3 | 2019 |
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 | 3 | 2019 |