Researchers
Pavlović, Sonja
Results 21-40 of 426
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | PHARMACOGENOMIC LANDSCAPE OF THE SERBIAN POPULATION | Zukić, Branka | Conference Paper | Mp. category will be shown later |
| 2025 | Significance of GSTM1 and GSTT1 Gene Deletions in Glioma Patients in Polish Population: Pilot Study | Todosijević Jovanović, Jovana; Gašić, Vladimir | Article | 22M22 |
| 2025 | Exploring the relationship between HLA variants and vedolizumab response in Crohn’s disease patients | Stašuk, Mihajlo | Conference Paper | Mp. category will be shown later |
| 2025 | Multiphasic acute disseminated encephalomyelitis (MDEM) in a patient with systemic lupus erythematosus and C4A deficiency: case-based review![]() | Ljubičić, Jelena | Article | 21M21 |
| 2025 | Efficiency of two available kits for amplification of three EGFR SNPs in patients with NSCLC: 181946 G/A (rs2293347), -191 C/A (rs712830) and -216G/T (rs712829) with GC-rich regions![]() | Jurišić, V. | Article | 23M23 |
| 2025 | Comprehensive pharmacogenomics profiling of the Serbian population | Jelovac, Marina | 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 |
| 2025 | Association of variants in candidate pharmacogenes with response to mercaptopurine and methotrexate drugs in pediatric ALL | Ćurić, Isidora | Conference Paper | Mp. category will be shown later |
| 2024 | The Relevance of β-Thalassemia Heterozygosity in Pediatric Clinical Practice: Croatian Experience | Đordević, Ana; Ugrin, Milena | Article | 21M21 |
| 2024 | GENETIC SPECTRUM OF NOONAN SYNDROME IN PEDIATRIC POPULATION | Ilić, Nikola; Krasić, Staša; Krstić, Jovana; Pavlović, Sonja | 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 | Can pharmacogenetics impact the therapeutic effect of cytarabine and anthracyclines in adult acute myeloid leukaemia patients?: A Serbian experience![]() | Pravdić, Zlatko; Suvajdžić-Vuković, Nada | Article | 23M23 |
| 2024 | CHARACTERIZATION OF 16 NOVEL GENETIC VARIANTS IN GENES ASSOCIATED WITH EPILEPSY | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2024 | GERMLINE VARIANTS IN CANCER PREDISPOSITION GENES IN PEDIATRIC PATIENTS WITH CENTRAL NERVOUS SYSTEM TUMORS![]() | Marjanović, Irena | Conference Paper | Mp. category will be shown later |
| 2024 | Novel telomerase reverse transcriptase gene mutation in a family with aplastic anaemia![]() | Virijevic, M | Article | 22M22 |
| 2024 | Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity | Stankovic, Sara | 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 | 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 | EXPLORING VARIATION IN ADHESION G PROTEIN-COUPLED RECEPTOR GENES: INSIGHTS FROM GENOMIC DATASETS OF PEDIATRIC RARE DISEASE CASES IN SERBIA | Pavlović, Đorđe | Conference Paper | Mp. category will be shown later |
| 2024 | GENETIC SPECTRUM OF PRIMARY DYSLIPIDEMIAS IN CHILDREN - SINGLE CENTER EXPERIENCE | Krstić, Jovana; Ilić, Nikola; Krasić, Staša; Gašić, Vladimir | Conference Paper | Mp. category will be shown later |
