Researchers
Skakić, Anita
Results 1-20 of 89
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | First Reported Use of Recombinant Parathyroid Hormone in Kenny–Caffey Syndrome Type 2: A Case Report and Literature Review | Milošević Đorđević, Maja; Skakić, Anita | Article | 22M22 |
| 2026 | The importance of elevated basal 17-hydroxyprogesterone in the diagnosis of children with congenital adrenal hyperplasia![]() | Miolski, Jelena; Ješić, Maja | Article | 23M23 |
| 2025 | Genetic testing for kidney disease-single centre experience![]() | Jovicic-Pavlovic, Svetlana; Nikolic, Jelena; Petrovic, Kristina; Stojadinovic, Milorad; Skakic, Anita | Conference Paper | Mp. category will be shown later |
| 2025 | Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model | Parezanovic, Marina V | Article | 22M22 |
| 2025 | Applications of the new tool: VUS Notifier | Domazet, Milan; Ugrin, Milena M; Andjelkovic, Marina Z; Klaassen, Kristel M; Skakic, Anita G | Conference Paper | Mp. category will be shown later |
| 2025 | Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor Therapy | Djordjevic-Milosevic, Maja; Skakic, Anita G | Article | 21M21 |
| 2025 | PULMONARY IN VITRO MODEL SYSTEM ENABLES EXPLORATION OF INNOVATIVE TREATMENT STRATEGIES FOR RARE RESPIRATORY DISEASES | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2025 | MITOCHONDRIAL MYOPATHY CAUSED BY MT-ND5 VARIANT: INTEGRATING WES AND MITOCHONDRIAL DNA ANALYSIS | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2025 | Thalassemia syndromes in Serbia:the importance of genetic (re)analysis | Ugrin, Milena M; Komazec, Jovana; Klaassen, Kristel M; Skakic, Anita G
Pavlovic, Sonja T; Stojiljkovic, Maja M;
| Conference Paper | Mp. category will be shown later |
| 2025 | ESTABLISHING IN VITRO MODELS FOR GLYCOGEN STORAGE DISEASE TYPE IB: A PLATFORM FOR THERAPEUTIC INVESTIGATIONS![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2025 | Advancing the IMGGE RD Biobank through BRIDGING-RD Project: Achieving full interoperability of genetic and phenotypic data to enhance participation in transnational research and innovation for human health | Komazec, Jovana | Conference Paper | Mp. category will be shown later |
| 2024 | Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies![]() | Anđelković, Marina | Article | 21M21 |
| 2024 | Genome sequence diversity of SARS-CoV-2 in Serbia: insights gained from a 3-year pandemic study![]() | Novković, Mirjana | Article | 21M21 |
| 2024 | Characterization of 16 novel genetic variants in genes associated with paediatric epilepsy: implications for targeted therapeutic strategies![]() | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2024 | Uloga glukozo-6-fosfat translokaze u procesu aktivacije autofagije kod glikogenoze tip Ib | Jocić, Nikola | Book parts | Mp. category will be shown later |
| 2024 | MOLECULAR BASIS OF PHENYLKETONURIA IN SERBIAN PAEDIATRIC COHORT | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2024 | WGS approach to identify potential genetic modifiers in Glycogen Storage Disease Ib![]() | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2024 | CHARACTERIZATION OF 16 NOVEL GENETIC VARIANTS IN GENES ASSOCIATED WITH EPILEPSY | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2024 | Genetic landscape of phenylketonuria in Serbia![]() | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2024 | Molecular genetic basis of childhood epilepsy in Serbia: utility of clinical and whole exome sequencing![]() | Anđelković, M. | Conference Paper | Mp. category will be shown later |
