Researchers
Marjanović, Ana
Results 21-40 of 101
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | Distonija-ataksija sindrom ranog početka kao manifestacija POLR3a povezane leukodistrofije | Šarčević, Maksim; Milovanović, Andona  ; Branković, Marija  ; Mazalica, Nina; Marković, Vladana ; Tomić, Aleksandra ; Marjanović, Ana ; Dragašević-Mišković, Nataša | Conference Paper | Mp. category will be shown later |
| 2024 | APOE genotype, ATXN1 and ATXN2 repeats size in C9orf72 expansion carriers | Marjanović, Ana ; Mandić-Stojmenović, Gorana ; Virić, Vanja ; Branković, Marija ; Janković, Milena ; Stojković, Tanja ; Novaković, Ivana ; Stević, Zorica ; Stefanova, Elka | Conference Paper | Mp. category will be shown later |
| 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 | 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 | 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 |
| 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 |
| 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 | 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 | 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 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 | 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 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 | Clinical phenotype of amyotrophic lateral sclerosis with C9ORF72 repeat expansion in Serbia | Virić, Vanja ; Palibrk, Aleksa; Marjanović, Ana ; Božović, Ivo ; Ivanović, Vukan ; Perić, Stojan ; Basta, Ivana ; Janković, Milena ; Novaković, Ivana ; Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2023 | The importance of direct genetic testing to determine female carriers in dystrophinopathies | Maksić, Jasmina ; Maksimović, Nela ; Rasulić, Lukas ; Milankov, Olgica; Marjanović, Ana ; Cvetković, Dragana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana | Article | 23M23 |
| 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 | 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+ |
| 2023 | Zastupljenost ekspanzija heksanukleotidnih ponovaka u nekodirajućem regionu gena C9orf72 kod različitih neurodegenerativnih bolesti | Marjanović, Ana | Doctoral theses | 70M70 |
| 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 |