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Research outputs
Triptorelin Test in Idagnosing Central Precocious Puberty
[2018]
Vuković, Rade M.; Milenković, Tatjana; Mitrović, Katarina; Todorović, Slađana; Plavšić, Ljiljana; Soldatović, Ivan A. 
Severe Adrenocortical Carcinoma Presentation with Vena Cava Involvement in a 1-Year-Old Boy: A Case Presentation and Management Considerations [2024]
Cvetkovic, Dimitrije; Vukovic, Rade; Milenkovic, Tatjana; Todorovic, Sladjana; Mitrovic, Katarina; Panic-Zaric, Sanja; Cehic, Maja; Djokic, Dragomir; Redzic, Danka; Aleksic, Dragana S;
Radeta, Ratko ; ...; (broj, koautora 17);
; ...; (broj, koautora 17); Very early and atypical presentation of Triple A (Allgrove) syndrome
[2022]
Cehić, Maja; Kovačević, Gordana ; Milenković, Tatjana; Kravljanac, Ružica ; Todorović, Slađana; Vuković, Rade; Panić-Zarić, Sanja; Mitrović, Katarina
Global Practice of Glucocorticoid and Mineralocorticoid Treatment in Children and Adults with Congenital Adrenal Hyperplasia - Insights from the I-CAH Registry [2019]
Bacila, Irina-Alexandra; ...; Milenkovic, Tatjana; ...; (broj, koautora 36)Development Of An International Benchmark For Sick Day Episodes As A Core Clinical Outcome In People With Congenital Adrenal Hyperplasia [2019]
Ali, Salma R; ...; Milenkovic, Tatjana; ...; (broj, koautora 41)Unusually enlarged ovaries associated with severe hypothyroidism - Van wyk and grumbach syndrome case report [2022]
Cvetkovic, Dimitrije; Todorovic, Sladjana; Milenkovic, Tatjana; Mitrovic, Katarina; Vukovic, Rade M; Panic-Zaric, Sanja; Savic, Djordje; Mijovic, Tanja; Smolovic, Dijana S; Toncev, JovanaInfluence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry [2019]
Neumann, Uta; ...; Milenkovic, Tatjana; ...; (broj, koautora 27)Why Is the Thyroid So Prone to Autoimmune Disease?
[2011]
Saranac, Ljiljana; Zivanovic, Snezana S ; Bjelakovic, Bojko B ; Stamenkovic, Hristina M ; Novak, Martin; Kamenov, Borislav A
A Novel GH1 Mutation in a Family with Isolated Growth Hormone Deficiency Type II [2012]
Gucev, Zoran; Tasic, Velibor; Šaranac, Ljiljana; Stobbe, Heike; Kratzsch, Jürgen; Klammt, Jürgen; Pfäffle, Roland
A male infant with X- linked congenital adrenal hypoplasia and Xp 21 contiguous gene deletion syndrome- case report [2023]
Stojkovic, Milica; Markovic, Aleksandar; Golubovic, Milan B; Ognjanovic, Andjela; Andrejevic, Marija; Jakovljevic, Milica; Cvetkovic, Vesna; Stankovic, Sandra MФилтери
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