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Browsing by Author Stanković, Sara
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | Application of CRISPR/cas9 technology for in vitro disease modelling in glycogen storage disease type IB![]() | Parezanović, Marina | 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 |
| 2023 | Functional characterization of novel variants in the dnai1 gene in a patient with primary ciliary dyskinesia![]() | Skakić, Anita | 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 |
| 2025 | Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant | Klaassen, K | Article | 21M21 |
| 2023 | High-risk population screening for fabry disease in patients with chronic renal failure of unknown etiology![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2025 | Integration of federated learning to study of pathologies with intellectual disabilities within the European BETTER Consortium![]() | Barco-Armengol, Nidia; ...; Stojiljkovic, Maja M | Conference Paper | Mp. category will be shown later |
| 2023 | Investigation of the role of the glucose-6-phosphate translocase in the activation of autophagy and glycogen-selective autophagy in glycogen storage disease type IB patients![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2026 | Ispitivanje patofiziologije i terapijskih strategija za glikogenozu tip Ib upotrebom CRISPR/Cas9 i iPSC model sistema![]() | Parezanović, Marina | 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 |
| 2023 | Molecular basis of phenylketonuria in Serbia: an update![]() | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2023 | Molecular basis of thalassemia syndromes in Serbia: an update![]() | Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 2026 | Phenylketonuria: Importance of neonatal screening, insights into genotype-phenotype correlations, and novel therapeutic approaches![]() | Đorđević, Milošević | Article | Mp. category will be shown later |
| 2026 | Pregled metaboličkih retkih bolesti detektovanih u Srbiji radi odabira najpogodnijih bolesti za pravljenje novog hepatičnog modela bolesti baziranog na iPSC | Grujić, Kristina | Conference Paper | Mp. category will be shown later |
| 2026 | RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3![]() | Kravljanac, Ruzica M; Klaassen, Kristel M | Article | 22M22 |
| 2026 | Sekvenciranje kompletnog genoma dugim očitavanjima (LR-WGS) u cilju preciznije molekularno-genetičke dijagnoze kongenitalne adrenalne hiperplazije![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2025 | Thalassemia syndromes in Serbia:the importance of genetic (re)analysis![]() | Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 2023 | The role of MIR-34 family members on the mucociliary process in the cellular respiratory model system![]() | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2024 | Transcriptome profile of phenylalanine treated NT2-derived neurons – a step towards novel PKU model system PO-576 | Stanković, Sara | Conference Paper | Mp. category will be shown later |
| 2024 | Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity | Stankovic, Sara | Article | 21M21 |
