Researchers
Ješić, Maja
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2021 | Neonatal diabetes mellitus due to a new KCNJ11 mutation - 10 years of the patient's follow-up | Ješić, Maja D.   ; Stock, Helena; Zdravković, Vera M. ; Kovačević, Smiljka; Savić, Marko D. ; Ješić, Miloš M. | Article | 23M23 |
| 2017 | First patient in Serbia with biochemically and genetically diagnosed pyridoxine-dependent epilepsy | Ješić, Miloš ; Ješić, Maja ; Buljugić, Svetlana; Živanović, Aleksandra | Article | 23M23 |
| 2016 | Duration of valproic acid monotherapy correlates with subclinical thyroid dysfunction in children with epilepsy | Ilić, V; Bogićević, Dragana ; Miljković, Branislava ; Ješić, M ; Kovačević, M; Prostran, Milica ; Vezmar-Kovačević, Sandra | Article | 23M23 |
| 2015 | Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations | Milacic, I.; Barac, M.; Milenkovic, T.; Ugrin, Milena ; Klaassen, Kristel ; Skakić, Anita ; Ješić, Maja ; Joksic, I.; Mitrovic, K.; Todorovic, S.;
Vujović, Svetlana
; Pavlović, Sonja ; Stojiljković, Maja ; | Article | 23M23 |
| 2014 | Prophylactic thyroidectomy for asymptomatic 3-year-old boy with positive multiple endocrine neoplasia type 2A mutation (codon 634) | Ješić, Maja ; Tančić-Gajić, Milina ; Ješić, Miloš ; Živaljević, Vladan ; Sajić, Silvija ; Vujović, Svetlana ; Damjanović, Svetozar | Article | 23M23 |