Researchers
Svetel, Marina
Results 1-20 of 321
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Retinal Thickness Profiles in Parkinsonian Syndromes: Discerning Parkinson's Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy via Optical Coherence Tomography | Svetel, Marko; Marić, Gorica   ; Božić, Marija M. ; Pekmezović, Tatjana ; Petrović, Igor ; Jakšić, Jana; Dimitrijević, Ana; Lazić, Una ; Kostić, Smiljana ; Knežević, Milica;
Petrović, Tiana; Petrović-Pajić, Sanja; Šobot, Vesna R.; Vasilijević, Jelena B.
; Svetel, Marina ; | Article | 21M21 |
| 2026 | Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease | Bergant, Gaber; ...; Branković, Marija ; Janković, Milena Z. ; Svetel, Marina ; ...; Dragašević-Mišković, Nataša ; Petrović, Igor ; ...; Novaković, Ivana ;
...; (broj koautora 19);
| Article | 22M22 |
| 2025 | The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson's disease | Radojević, Branislava ; Milovanović, Andona ; Petrović, Igor N. ; Svetel, Marina V. ; Marjanović, Ana ; Jančić, Ivan ; Stanisavljevic, Dejana M ; Milićević, Ognjen S. ; Savić, Miroslav ; Kostić, Vladimir S. ;
Dragašević-Mišković, Nataša T.
; | Article | 22M22 |
| 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 ; Todorović, Slobodanka ; Novaković, Ivana ; Dobričić, Valerija ; Savić-Pavićević, Dušanka ; Milić-Rašić, Vedrana ; Svetel, Marina ; Brkušanin, Miloš ; Vukomanović, Vladislav ; Vučinić, Dragana;
Ostojić, Slavica; Putnik, Jovana; Kosać, Ana
; | Article | 21M21 |
| 2025 | Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease | Kovanda, Anja; Šušmelj, Lara; Jaklič, Helena; Lukežič, Tadeja; Maver, Aleš; Petrović, Igor N. ; Dragašević-Mišković, Nataša T. ; Svetel, Marina V. ; Racki, Valentino; Vuletič, Vladimira;
Novakovič, Ivana V.
; Peterlin, Borut; | Contribution to periodical | 22M22 |
| 2025 | Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population | Kovanda, Anja; Šušmelj, Lara; Lukežič, Tadeja; Maver, Aleš; Rački, Valentino; Vuletić, Vladimira; Svetel, Marina V. ; Novaković, Ivana ; Peterlin, Borut | Conference Paper | Mp. category will be shown later |
| 2025 | Copper speciation and total essential trace element levels in Wilson's disease | Stojsavljević, Aleksandar ; Kozlica, Katarina; Šarac, Ivana ; Lazić, Una ; Vitković, Jelena; Radišić, Vanja ; Polović, Natalija ; Svetel, Marina ; Ščančar, Janez | Article | 21M21 |
| 2025 | Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease? | Kresojević, Nikola ; Marković, Vladana ; Geratović, Cveta; Ječmenica-Lukić, Milica ; Tomić, Aleksandra ; Dobričić, Valerija ; Stanković, Iva D. ; Stojkovic, Tanja ; Dragašević, Nataša ; Šarčević, Maksim;
Jankovic, Milena
; Marjanovic, Ana ; Novaković, Ivana ; Kostić, Vladimir ; Svetel, Marina ; Petrović, Igor ; | Article | 22M22 |
| 2024 | RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia | Milovanović, Andona ; Dragašević-Mišković, Nataša T. ; Thomsen, Mirja; Borsche, Max; Hinrichs, Frauke; Westenberger, Ana; Klein, Christine; Brueggemann, Norbert; Branković, Marija ; Marjanović, Ana ;
Svetel, Marina V.
; Kostić, Vladimir S. ; Lohmann, Katja; | Article | 21M21 |
| 2024 | Challenges in rare diseases: The example of mitochondrial diseases | Novaković, Ivana ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Svetel, Marina ; Jančić, Jasna | Conference Paper | Mp. category will be shown later |
| 2024 | Osnovi neurološkog pregleda | Kostić, Vladimir ; Jovanović, Dejana ; Vojvodić, Nikola M. ; Beslać-Bumbaširević, Ljiljana ; Cerovac, Nataša ; Čovičković-Šternić, Nadežda ; Dragašević-Mišković, Nataša ; Drulović, Jelena ; Jančić, Jasna ; Jovanović, Zagorka ;
Jović, Nebojša J.
; Lavrnić, Dragana ; Mesaroš, Šarlota ; Milić-Rašić, Vedrana ; Pavlović, Dragan M. ; Rakočević-Stojanović, Vidosava ; Sokić, Dragoslav ; Stefanova, Elka ; Stević, Zorica ; Svetel, Marina ; Zidverc-Trajković, Jasna ; | Text book | Mp. category will be shown later |
| 2024 | Intraocular pressure in patients suffering from Wilson's disease | Božić, Marija M. ; Svetel, Marina V. ; Svetel, Marko | Article | 22M22 |
| 2024 | Genotype-phenotype correlation in PRKN-associated Parkinson's disease | Menon, Poornima Jayadev; ...; Jovanović, Čarna; Svetel, Marina V. ; ...; (broj koautora 53) | Article | 21aM21a |
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series | Milovanović, Andona ; Westenberger, Ana; Stanković, Iva D. ; Tamaš, Olivera S.; Branković, Marija ; Marjanović, Ana ; ...; Branković, Vesna; Novaković, Ivana V. ; Petrović, Igor N. ;
Svetel, Marina V.
; Klein, Christine; Kostić, Vladimir S. ; Dragašević-Mišković, Nataša T. ; (broj koautora 18); | Article | 21a+M21a+ |
| 2024 | Early Screening for the Parkinson Variant of Multiple System Atrophy: A 6-Item Score | Fanciulli, Alessandra; Stanković, Iva D. ; ...; Ječmenica-Lukić, Milica V. ; ...; Petrović, Igor N. ; Svetel, Marina V. ; ...; Kostić, Vladimir K. ; ...;
(broj koautora 16);
| Article | 21M21 |
| 2024 | Structural brain heterogeneity underlying symptomatic and asymptomatic genetic dystonia: a multimodal MRI study | Tomić, Aleksandra D. ; Sarasso, Elisabetta; Basaia, Silvia; Dragašević-Mišković, Nataša T. ; Svetel, Marina V. ; Kostić, Vladimir S. ; Filippi, Massimo; Agosta, Federica | Article | 21aM21a |
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia | Branković, Marija ; Ivanović, Vukan ; Basta, Ivana ; Khang, Rin; Lee, Eugene; Stević, Zorica ; Ralić, Branislav; Tubić, Radoje ; Seo, GoHun; Marković, Vladana ;
Božović, Ivo
; Svetel, Marina ; Marjanović, Ana ; Veselinović, Nikola; Mesaroš, Šarlota ; Janković, Milena ; Savić-Pavićević, Dušanka ; Jovin, Zita; Novaković, Ivana ; Lee, Hane; Perić, Stojan ; | Article | 22M22 |
| 2024 | Analysis of clinical exome panel in rare movement and cognitive disorders | Branković, Marija ; Dragašević, Nataša ; Svetel, Marina ; Stefanova, Elka ; Mandić, Gorana ; Stojković, Tanja ; Milovanović, Andona ; Marković, Vladana ; Janković, Milena ; Marjanović, Ana ;
Dobričić, Valerija
; Novaković, Ivana ; Kostić, Vladimir ; | Conference Paper | Mp. category will be shown later |
| 2024 | Motor imagery ability in patients with functional dystonia | Tomić, Aleksandra ; Ječmenica-Lukić, Milica ; Petrović, Igor ; Korkut, Vladimir; Kresojević, Nikola ; Marković, Vladana ; Dragašević-Mišković, Nataša ; Svetel, Marina ; Kostić, Vladimir S. | Article | 21M21 |
| 2024 | Patterns of neuropsychiatric symptoms in primary and secondary tauopathies: Caregiver and patient perspectives | Ječmenica-Lukić, Milica ; Mandić, Gorana ; Stojković, Tanja ; Tomić, Aleksandra ; Marković, Vladana ; Stanković, Iva; Kresojević, Nikola ; Petrović, Igor ; Kačar, Aleksandra ; Dragašević, Nataša ;
Kostić, Vladimir; Svetel, Marina
; | Article | 53M53 |