Researchers
Anđelković, Marina
Results 21-40 of 82
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | Ultra-Early Diffuse Lung Disease in an Infant with Pathogenic Variant in Telomerase Reverse Transcriptase (TERT) Gene![]() | Višekruna, Jelena; Baša, Mihail; Grba, Tijana; Anđelković, Marina | Article | 23M23 |
| 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 | 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 | New TERT variant in a family with aplastic anemia![]() | Virijević, Marijana | 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 | Seven-Year Longitudinal Study: Clinical Evaluation of Knee Osteoarthritic Patients Treated with Mesenchymal Stem Cells![]() | Spasovski, Duško | Article | 21M21 |
| 2024 | MOLECULAR BASIS OF PHENYLKETONURIA IN SERBIAN PAEDIATRIC COHORT | Klaassen, Kristel | 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 | Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies![]() | Anđelković, Marina | Article | 21M21 |
| 2023 | Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs data | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | THE IMPACT OF NEXT-GENERATION SEQUENCING ON DIAGNOSIS AND TREATMENT OF RARE DISEASES | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2023 | Congenital central hypoventilation syndrome: Heterogeneous clinical presentation, ventilatory modalities and outcome![]() | Mihail Basa; Jelena Visekruna; Bojana Gojsina; Tijana Grba; Andjelkovic, Marina | Article | 53M53 |
| 2023 | Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology![]() | Parezanović, Marina | 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 | Molecular basis of thalassemia syndromes in Serbia: an update![]() | Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 2023 | Unique pipeline for the assessment of novel genetic variants leads to confirmation of PCD diagnosis | Stevanović, Nina | 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 phenylketonuria in Serbia: an update![]() | Klaassen, Kristel | 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 |
