Researchers
Savić-Pavićević, Dušanka
Results 21-40 of 310
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia![]() | Kovačević, Gordana | Article | 21M21 |
| 2025 | Genotype-sensitive dynamic model of the serotonin presynapse shows complex interplay between synapse metabolites | Radenković, Lana | Conference Paper | Mp. category will be shown later |
| 2024 | A comparative transcriptomic analysis of mouse DM1 models’ skeletal muscles![]() | Lazić, Dušan | Conference Paper | Mp. category will be shown later |
| 2024 | Diagnostic properties of miR-146a-5p from liquid biopsies in prostate cancer: A meta-analysis![]() | Dobrijević, Zorana | Article | 21M21 |
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Branković, Marija | Article | 22M22 |
| 2024 | COMPREHENSIVE GENETIC STUDY IDENTIFIES DIFFERENT SUSCEPTIBILITY FACTORS FOR EARLY- AND LATE-ONSET ACETYLCHOLINE POSITIVE MYASTHENIA GRAVIS PATIENTS FROM SERBIA | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2024 | Somatic Instability of CTG Repeats Over Time in Blood Cells of DM1 Patients | Radovanović, Nemanja | Conference Paper | Mp. category will be shown later |
| 2024 | Modal allele change as a predictor of skeletal muscle symptoms progression in myotonic dystrophy type 1![]() | Radovanović, N.; Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2024 | Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma as a Nusinersen treatment response marker in childhood-onset SMA individuals from Serbia![]() | Brkušanin, Miloš | Article | 21M21 |
| 2024 | Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity | Nunez, Manchon Judit; ...; Pesovic, Jovan; ...; Savic-Pavicevic, Dusanka Lj | Article | 21aM21a |
| 2024 | Mood disorders and 5-HTR2A genetic variants – the moderator effect of inflammation on expression of affective polarity phenotype![]() | Pantović-Stefanović, Maja; Karanović, Jelena | Article | 21M21 |
| 2024 | 469P Modal allele change as a predictor of skeletal muscle symptoms progression in myotonic dystrophy type 1 | Radovanović, Nemanja | Conference Paper | Mp. category will be shown later |
| 2024 | Our Journey from Individual Efforts to Nationwide Support: Implementing Newborn Screening for Spinal Muscular Atrophy in Serbia | Brkušanin, Miloš | Article | 21aM21a |
| 2024 | Single-molecule RNA sizing enables quantitative analysis of alternative transcription termination![]() | Patiño-Guillén, Gerardo; Pešović, Jovan; Panić, Marko | Article | 21aM21a |
| 2024 | Revolutionizing Spinal Muscular Atrophy Prevention in Serbia: Implementing a Mandatory Statewide Newborn Screening![]() | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2024 | Genetic predisposition of suicidal behavior: variants in GRIN2B, GABRG2, and ODC1 genes in attempted and completed suicide in two Balkan populations | Karanović, Jelena
Videtič Paska, Alja;
| Article | 21M21 |
| 2024 | CRISPR-Cas9 generated cell lines for myotonic dystrophy type 1 modeling![]() | Ninković, Anastasija | Conference Paper | Mp. category will be shown later |
| 2024 | Association between Cytotoxic T-Lymphocyte-Associated Antigen 4 (CTLA-4) Locus and Early-Onset Anti-acetylcholine Receptor-Positive Myasthenia Gravis in Serbian Patients![]() | Đorđević, Ivana; Garai, Nemanja | Article | 21M21 |
| 2024 | Main features and disease outcome of congenital myotonic dystrophy- experience from a single tertiary center![]() | Ostojić, Slavica B.; Kovačević, Gordana S. | Article | 22M22 |
| 2024 | METHYLATION OF CCG VARIANT REPEATS IS ASSOCIATED WITH HETEROGENEOUS METHYLATION OF CPG SITES SURROUNDING DMPK EXPANSION IN MYOTONIC DYSTROPHY TYPE 1 PATIENTS | Pešović, J.; Bashtrykov, P.; Perić, S.; Radenković, Lana | Conference Paper | Mp. category will be shown later |
