Researchers
Pešić, Milica
Results 1-20 of 33
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral Palsy![]() | Đuranović-Uklein, Ana S. | Article | 21M21 |
| 2025 | Association of NOS Gene Polymorphisms with Sepsis-Related Complications in Secondary Peritonitis![]() | Rašić, Milica | Article | 21M21 |
| 2025 | New evidence supporting female protective effect in patients with congenital anomalies and neurodevelopmental disorders![]() | Maksimović, Nela | Article | 21M21 |
| 2024 | Sleep problems in female carriers of premutation in the FMR1 gene![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2024 | Analysis of the association between MMP-8 gene polymorphisms and the occurrence of adverse effects after acute ischemic stroke treated with recombinant tissue plasminogen activator![]() | Dušanović-Pjević, Marija G. | Conference Paper | Mp. category will be shown later |
| 2024 | R47H TREM2 variant among Serbian Alzheimer's disease patients![]() | Andrejić, Nikola | Conference Paper | Mp. category will be shown later |
| 2023 | Drosophila Melanogaster Model for the study of Fragile X Syndrome![]() | Makević, Vedrana | Conference Paper | Mp. category will be shown later |
| 2023 | Drosophila melanogaster as a Model to Study Fragile X-Associated Disorders![]() | Trajković, Jelena | Article | 22M22 |
| 2023 | Probing the fragile X syndrome in Drosophila using a new platform for circadian rhythm and sleep research with videography![]() | Milojević, Sara | Conference Paper | Mp. category will be shown later |
| 2023 | The association of R47H variant in the TREM2 gene and genetic susceptibility to Alzheimer's disease in Serbian population![]() | Andrejić, Nikola; Pešić, Milica | Article | 53M53 |
| 2023 | TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2023 | Human Genetics![]() | Cvjetićanin, Suzana | Text book | Mp. category will be shown later |
| 2021 | Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism![]() | Pešić, Milica | Article | 22M22 |
| 2021 | TT genotype of the MMP-9-1562C/T polymorphism may be a risk factor for thrombolytic therapy-induced hemorrhagic complications after acute ischemic stroke![]() | Dušanović-Pjević, Marija G.
Kačar, Katarina;
| Article | 21M21 |
| 2020 | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1β, andTNF-α in relation with Parkinson’s disease progression![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2020 | Analysis of the association within MMP-2 gene polymorphisms and ischemic stroke outcome after thrombolytic therapy![]() | Dušanović-Pjević, Marija G. | Conference Paper | Mp. category will be shown later |
| 2020 | Analysis of association of MMP-2 gene promoter haplotype with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis![]() | Grk, Milka B. | Conference Paper | Mp. category will be shown later |
| 2020 | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2020 | Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis![]() | Grk, Milka | Article | 21M21 |
| 2020 | Investigation of the MMP2 haplotype as a risk factor for the development of cerebral palsy![]() | Đuranović, Ana S. | Conference Paper | Mp. category will be shown later |
