Researchers
Anđelković, Marina
Results 41-60 of 82
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | Molecular basis of thalassemia syndromes in Serbia: an update![]() | Ugrin, Milena | 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 | 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 | 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 | 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 |
| 2023 | New TERT variant in a family with aplastic anemia![]() | Virijević, Marijana | 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 |
| 2022 | Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier![]() | Kristel Klaassen | Conference Paper | Mp. category will be shown later |
| 2022 | Crosstalk between Glycogen-Selective Autophagy, Autophagy and Apoptosis as a Road towards Modifier Gene Discovery and New Therapeutic Strategies for Glycogen Storage Diseases![]() | Anđelković, Marina | Article | 21M21 |
| 2022 | Retke bolesti u eri genomike | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2022 | Dizajniranje jedinstvenih smernica za standardizaciju analize NGS podataka kod pacijenata sa retkim plućnim bolestima | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2022 | Association between active pulmonary tuberculosis and miRNA-146a: A preliminary study from Serbia![]() | Buha, Ivana; Škodrić-Trifunović, Vesna | Article | Mp. category will be shown later |
| 2022 | Funkcionalna karatkerizacija novootkrivenih varijanti u genu DNAI1 kod pacijenta sa primarnom cilijarnom diskinezijom | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2022 | Molekularna dijagnostika Fabrijeve bolesti kod pacijenata sa hroničnom bubrežnom insuficijencijom nepoznate etiologije![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2022 | Диференцијална дијагноза педијатријских болесника са болестима плућа коришћењем секвенцирања нове генерације![]() | Анђелковић, Марина | Conference Paper | Mp. category will be shown later |
| 2021 | Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA![]() | Đurić, Olivera | Article | 21M21 |
| 2021 | Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary Dyskinesia![]() | Stevanović, Nina | Article | 21M21 |
| 2021 | Molekularna osnova primarne cilijarne diskinezije | Anđelković, Marina | Book parts | Mp. category will be shown later |
| 2020 | Correlation of expression of TLR7 and Mirna-146a genes and fibrosis in peripheral blood and skin samples of SSc patients![]() | Vesna Spasovski | Conference Paper | Mp. category will be shown later |
| 2020 | Genetička osnova otoskleroze | Zukić, Branka | Article | 23M23 |
