Претрага
Резултати
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 MInsulin Resistance in Prepubertal Children
[2017]
Zdravković, Vera M. Clinical and molecular genetic characteristics of monogenic diabetes cases - single European center experience [2025]
Zdravkovic, VA Novel GH1 Mutation in a Family with Isolated Growth Hormone Deficiency Type II [2012]
Gucev, Zoran; Tasic, Velibor; Šaranac, LjiljanaHabits and safety issues concerning alcohol consumption and gaps in diabetes education in young people with type 1 diabetes - preliminary findings of T1Drink study [2024]
Wykrota, J; ...; Vukovic, R; Panic-Zaric, Sanja; ...; (broj, koautora 25)Identification of novel genetic causes of familial central precocious puberty
[2021]
Avbelj-Stefanija, Magdalena; ...; Milenković, Tatjana; Vuković, Rade M.; Todorović, Slađana; ...; Zdravković, Vera M.
(broj koautora 17);
Very early and atypical presentation of Triple A (Allgrove) syndrome
[2022]
Cehić, Maja; Kovačević, Gordana Renal Functional Reserve in Children with Type 1 Diabetes
[2016]
Zdravković, Vera Hyperprolactinemia: Different Clinical Expression in Childhood
[2010]
Šaranac, Ljiljana The first case of pediatric Cushing disease in Serbia
[2022]
Panic-Zaric, Sanja Филтери
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