Researchers
Klaassen Ljubičić, Kristel
Results 21-40 of 102
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Multiphasic acute disseminated encephalomyelitis (MDEM) in a patient with systemic lupus erythematosus and C4A deficiency: case-based review![]() | Ljubičić, Jelena | Article | 21M21 |
| 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 | Conference Paper | Mp. category will be shown later |
| 2025 | Heterologous expression of human glucose-6-phosphate translocase (SLC37A4) in prokaryotic and yeast systems | Stanišić, Marija; Ugrin, Milena | 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 |
| 2024 | WGS approach to identify potential genetic modifiers in Glycogen Storage Disease Ib![]() | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2024 | Transcriptome profile of phenylalanine treated NT2-derived neurons – a step towards novel PKU model system![]() | Kristel Klaassen | 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 | Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity | Stankovic, Sara | Article | 21M21 |
| 2024 | INVESTIGATING THE GENETIC COMPLEXITY OF NEUTROPENIA IN PEDIATRIC PATIENTS WITH GLYCOGEN STORAGE DISEASE IB: A MODIFIER GENE PERSPECTIVE | Skakić, Anita | 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 | 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 | Case report: Rapidly progressive neurocognitive disorder with a fatal outcome in a patient with PU.1 mutated agammaglobulinemia![]() | Mišković, Rada | Article | 21M21 |
| 2024 | Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies![]() | Anđelković, Marina | Article | 21M21 |
| 2024 | MOLECULAR BASIS OF PHENYLKETONURIA IN SERBIAN PAEDIATRIC COHORT![]() | Klaassen, Kristel | 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 |
| 2023 | CHARACTERIZATION OF 16 NOVEL GENETIC VARIANTS IN GENES RELATED TO CHILDHOOD EPILEPSIES | Anđelković, Marina | 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 |
| 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 |
| 2023 | Differential expression of TLR7 and miRNA-146a genes in peripheral blood and skin samples of patients with systemic sclerosis![]() | Spasovski, Vesna M | Conference Paper | Mp. category will be shown later |
