Researchers
Dobričić, Valerija
Type
Date issued
Results 1-20 of 89
| 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   ; 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 | 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 | Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center | Stefanova, Elka D. ; Marjanović, Ana ; Dobričić, Valerija S. ; Mandić-Stojmenović, Gorana B. ; Stojković, Tanja ; Branković, Marija ; Šarčević, Maksim; Novaković, Ivana V. ; Kostić, Vladimir S. | 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 | C9orf72 genetic screening in patients with ALS/FTD phenotype from Serbia | Marjanović, Ana ; Mandić-Stojmenović, Gorana ; Milićević, Ognjen ; Stojković, Tanja ; Virić, Vanja ; Janković, Milena ; Branković, Marija ; Palibrk, Aleksa ; Ivanović, Vukan ; Dobričić, Valerija ;
Perić, Stojan
; Novaković, Ivana ; Stević, Zorica ; Stefanova, Elka ; | Conference Paper | Mp. category will be shown later |
| 2023 | Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian population | Branković, Marija ; Dragašević, Nataša ; Svetel, Marina ; Milovanović, Andona ; Marković, Vladana ; Janković, Milena ; Marjanović, Ana ; Dobričić, Valerija ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2023 | C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia | Marjanović, Ana ; Palibrk, Aleksa; Dobričić, Valerija ; Milićević, Ognjen ; Branković, Marija ; Virić, Vanja ; Drinić, Aleksandra; Mandić-Stojmenović, Gorana ; Janković, Milena ; Basta, Ivana ;
Perić, Stojan
; Novaković, Ivana ; Stefanova, Elka ; Stević, Zorica ; | Article | 22M22 |
| 2023 | Motor neuron involvement in facial muscles as characteristic of ANO10 mutation | Dragašević-Mišović, Nataša ; Milovanović, Andona ; Stanković, Iva ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija S. ; Petrović, Igor N. ; Svetel, Marina V. ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2023 | Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism” | Kresojević, Nikola ; Marković, Vladana ; Dobričić, Valerija ; Stanković, Iva ; Stojković, Tanja ; Tomić, Aleksandra ; Ječmenica-Lukić, MIlica ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ;
Novaković, Ivana
; Petrović, Igor ; Dragašević, Nataša ; Svetel, Marina ; Kostić, Vladimir ; | Article | 21a+M21a+ |
| 2022 | C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population | Marjanović, Ana ; Dobričić, Valerija ; Ječmenica-Lukić, Milica ; Stanković, Iva ; Milićević, Ognjen ; Dragašević-Mišković, Nataša ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Svetel, Marina ;
Stefanova, Elka
; Kostić, Vladimir ; | Article | 22M22 |
| 2022 | Analysis of “clinical exome” panel in Serbian patients with cognitive disorders | Branković, Marija ; Stefanova, Elka ; Mandić, Gorana ; Marjanović, Ana ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Stević, Zorica ; Janković, Milena ; Novaković, Ivana ;
Peterlin, Borut; Kostić, Vladimir
; | Article | 22M22 |
| 2022 | Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience | Branković, Marija ; Dragašević, Nataša ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Petrović, Igor ; Perić, Stojan ; Marjanović, Ana ; Janković, Milena ; Jančić, Jasna ;
Novaković, Ivana
; Peterlin, Borut; Svetel, Marina ; Kostić, Vladimir ; | Article | 22M22 |
| 2022 | Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience | Kresojević, Nikola ; Dobričić, Valerija ; Ječmenica-Lukić, Milica ; Tomić, Aleksandra ; Petrović, Igor ; Dragašević, Nataša ; Perović, Ivana; Marjanović, Ana ; Branković, Marija ; Janković, Milena ;
Novaković, Ivana
; Svetel, Marina ; Kostić, Vladimir S. ; | Article | 21aM21a |
| 2021 | Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism | Pešić, Milica ; Dragašević-Mišković, Nataša ; Marjanović, Ana ; Dobričić, Valerija ; Maksimović, Nela ; Svetel, Marina ; Perović, Dijana ; Novaković, Ivana ; Ćirković, Sanja; Stanković, Iva ;
Kostić, Vladimir
; | Article | 22M22 |
| 2021 | Selected genetic polymorphisms of COMT, DRD2, ANKK1, and DAT genes and the risk of psychosis in Parkinson's disease | Radojević, Branislava ; Dragašević, Nataša T. ; Milovanović, Andona ; Branković, Marija ; Svetel, Marina V. ; Dobričić, Valerija S. ; Petrović, Igor N. ; Savić, Miroslav ; Stanisavljević, Dejana M. ; Kostić, Vladimir K. | Conference Paper | Mp. category will be shown later |
| 2021 | Clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion | Marjanović, Ana ; Palibrk, Aleksa; Branković, Marija ; Janković, Milena ; Dobričić, Valerija ; Novaković, Ivana ; Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2021 | Clinical and Genetic Analysis of Psychosis in Parkinson’s Disease | Radojević, Branislava; Dragašević-Mišković, Nataša T. ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija ; Milovanović, Andona ; Tomić, Aleksandra ; Svetel, Marina ; Petrović, Igor ; Jančić, Ivan ;
Stanisavljević, Dejana
; Savić, Miroslav M. ; Kostić, Vladimir S. ; | Article | 21M21 |
| 2021 | Phenotype characteristics of ANO10 mutation carries: a case series from Serbia and a systematic review of the literature | Stanković, Iva ; Dragašević, Nataša ; Milovanović, Andona ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija ; Petrović, Igor ; Svetel, Marina ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2020 | Very Late-Onset Niemann Pick Type C Disease: Example of Progressive Supranuclear Palsy Look-Alike Disorder | Kresojević, Nikola D. ; Mandić-Stojmenović, Gorana B. ; Dobričić, Valerija S. ; Petrović, Igor N. ; Brajković, Leposava D. ; Stefanova, Elka D. ; Svetel, Marina V. ; Kostić, Vladimir K. | Article | 22M22 |
| 2020 | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies | Maksić, Jasmina ; Dobričić, Valerija ; Rasulić, Lukas ; Maksimović, Nela ; Branković, Marija ; Milić-Rašić, Vedrana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana | Article | 23M23 |