Researchers
Pavlović, Sonja
Results 41-60 of 420
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | Genome-wide association study identified genetic signal in cystatin genes associated with Long COVID-19 | Laban-Lazović, Marija; Zečević, Marko; Kotur, Nikola | 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 | Pharmacogenomic landscape of Serbian population | Jelovac, Marina | Conference Paper | Mp. category will be shown later |
| 2024 | POPULATION PHARMACOGENOMICS OF IMMUNOSUPPRESSIVE AND AMINOSALICYLATE THERAPY: POTENTIAL FOR THERAPY OPTIMIZATION IN SERBIAN PAEDIATRIC INFLAMMATORY BOWEL DISEASE PATIENTS | Jelovac, Marina | Conference Paper | Mp. category will be shown later |
| 2024 | The long non-coding RNA GAS5 contributes to the suppression of inflammatory responses by inhibiting NF-κB activity | Curci, Debora; Stanković, Biljana | Article | 21aM21a |
| 2024 | Case report: Rapidly progressive neurocognitive disorder with a fatal outcome in a patient with PU.1 mutated agammaglobulinemia![]() | Mišković, Rada | Article | 21M21 |
| 2024 | CAN NUDT15 BE PHARMACOGENETIC OR PHARMACOTRANSRIPTOMIC MARKER FOR 6- MERCAPTOPURINE IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA IN SERBIA | Ristivojević, Bojan | 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 | 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 |
| 2024 | Uticaj promotorskih varijanti gena za uridin-difosfat-glukuronoziltransferazu 1A1 na metabolizam bilirubina i značaj UGT1A1*28 varijante kao farmakogenetičkog markera | Vuković, Marija; Zukić, Branka | Book parts | Mp. category will be shown later |
| 2024 | Association of variants in AGTR1, ACE, MTHFR genes with microalbuminuria and risk factors for the onset of diabetic nephropathy in adolescents with type 1 diabetes in the population of Serbia![]() | Kovačević, Smiljka; Zdravković, Vera | Article | 21M21 |
| 2024 | Psychological Distress Is Associated With Inflammatory Bowel Disease Manifestation and Mucosal Inflammation | Dragašević, Sanja; Stanković, Biljana | Article | 21M21 |
| 2023 | Prognostic significance of cebpa mutations in patients with normal-karyotype - acute myeloid leukemia | Marjanović, Irena | Conference Paper | Mp. category will be shown later |
| 2023 | Presence of leukemic clone‐specific immunoglobulin heavy chain rearrangements in neonatal blood spots of children with B‐cell precursor acute lymphoblastic leukemia![]() | Kacanski, Natasa; Kolarovic, Jovanka | Article | 22M22 |
| 2023 | New TERT variant in a family with aplastic anemia![]() | Virijević, Marijana | 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 | The influence of BCL2, BAX, and ABCB1 gene expression on prognosis of adult de novo acute myeloid leukemia with normal karyotype patients![]() | Pravdic, Zlatko; Vukovic, Suvajdzic Nada; Gasic, Vladimir | 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 |
| 2023 | Rare metabolic diseases in the genomics era | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
