Researchers
Branković, Marija
Results 21-40 of 91
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | 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 | 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 | CYP2C9 screening: important step in siponimod treatment of secondary progressive multiple sclerosis | Janković, Milena ; Branković, Marija ; Marjanović, Ana ; Drulović, Jelena ; Novaković, Ivana | 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 | Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort | Kovačević, Maša ; Janković, Milena ; Branković, Marija ; Milićević, Ognjen S. ; Novaković, Ivana V. ; Sokić, Dragoslav V. ; Ristić, Aleksandar J. ; Berisavac, Ivana I. ; Vojvodić, Nikola M. | Conference Paper | Mp. category will be shown later |
| 2023 | Utvrđivanje genetičke osnove retkih neurodegenerativnih bolesti analizom kliničkog egzoma | Branković, Marija | Doctoral theses | 70M70 |
| 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 | EPR-210 Whole exome sequencing in Serbian patients with hereditary spastic paraplegia | Ivanović, Vukan ; Branković, Marija ; Božović, Ivo ; Stević, Zorica ; Basta, Ivana ; Marković, Vladana ; Svetel, Marina ; Tubić, Radoje ; Marjanović, Ana ; Veselinović, Nikola ;
Mesaroš, Šarlota
; Janković, Milena ; Rakočević-Stojanović, Vidosava ; Savić-Pavićević, Dušanka ; Novaković, Ivana ; Perić, Stojan ; | Conference Paper | Mp. category will be shown later |
| 2023 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia | Ivanović, Vukan ; Branković, Marija ; Božović, Ivo ; Stević, Zorica ; Basta, Ivana ; Marković, Vladana ; Svetel, Marina ; Tubić, Radoje ; Marjanović, Ana ; Veselinović, Nikola ;
Mesaroš, Šarlota
; Janković, Milena ; Rakočević-Stojanović, Vidosava ; Savić-Pavićević, Dušanka ; Novaković, Ivana ; Perić, Stojan ; | Conference Paper | Mp. category will be shown later |
| 2023 | C9ORF72 intermediate repats in neurodegenerative disorders from Serbia | Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Perić, Stojan ; Dragašević-Mišković, Nataša ; Mandić, Gorana ; Ječmenica-Lukić, Milica ; Stanković, Iva ; Stefanova, Elka ; Stević, Zorica ;
Novaković, Ivana
; Svetel, Marina ; Kostić, Vladimir ; | Conference Paper | Mp. category will be shown later |
| 2023 | Novel variants in established epilepsy genes in focal epilepsy | Kovačević, Maša ; Milićević, Ognjen ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Sokić, Dragoslav ; Ristić, Aleksandar ; Shamsani, Jannah; Vojvodić, Nikola | Article | 22M22 |
| 2023 | Novel GATOR1 variants in focal epilepsy | Kovačević, Maša ; Janković, Milena ; Branković, Marija ; Milićević, Ognjen ; Novaković, Ivana ; Sokić, Dragoslav ; Ristić, Aleksandar ; Shamsani, Jannah; Vojvodić, Nikola | 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 | Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience | Kresojević, Nikola ; Perović, Ivana; Stanković, Iva ; Tomić, Aleksandra ; Ječmenica-Lukić, Milica ; Marković, Vladana ; Stojković, Tanja ; Mandić, Gorana ; Janković, Milena ; Marjanović, Ana ;
Branković, Marija
; Novaković, Ivana ; Petrović, Igor ; Dragašević, Nataša ; Stefanova, Elka ; Svetel, Marina ; Kostić, Vladimir ; | Article | 21M21 |
| 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+ |
| 2023 | TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients | Pešić, Milica ; Andrejić, Nikola; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka | 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 ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka | Article | 53M53 |
| 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 | Employment status of patients with Charcot-Marie-Tooth type 1A | Bjelica, Bogdan ; Branković, Marija ; Božović, Ivo ; Palibrk, Aleksa; Kačar, Aleksandra ; Rakočević-Stojanović, Vidosava | Article | 22M22 |