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Browsing by Author Branković, Marija
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Issue Date | Title | Author(s) | Type | М-cat. |
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2022 | A multicenter study of genetic testing for Parkinson’s disease in the clinical setting (✓) | Kovanda, Anja; Rački, Valentino; Bergant, Gaber; Georgiev, Dejan; Flisar, Dušan; Papić, Eliša; Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21aM21a |
2023 | Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian population (✓) | Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2020 | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies (✓) | Maksić, Jasmina ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy (✓) | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2017 | Analysis of mtDNA mutations in Serbian patients with Lebers optic atrophy (✓) | Dawod, Phepy G. A.; Rovčanin, Branislav ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2018 | Analysis of pathogenic mtDNA mutations associated with Leber's hereditary optic neuropathy: our experience (✓) | Dawod, Phepy Gamil Anwar; Rovčanin, Branislav ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2022 | Analysis of “clinical exome” panel in Serbian patients with cognitive disorders (✓) | Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2019 | Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in Belgrade (✓) | Janković, Milena ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2019 | Body composition analysis in patients with myotonic dystrophy types 1 and 2 (✓) | Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 22M22 |
2023 | C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia (✓) | Marjanović, Ana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2023 | C9ORF72 intermediate repats in neurodegenerative disorders from Serbia (✓) | Marjanović, Ana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2022 | C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population (✓) | Marjanović, Ana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2021 | Clinical and Genetic Analysis of Psychosis in Parkinson’s Disease (✓) | Radojević, Branislava; Dragašević-Mišković, Nataša T. ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21M21 |
2023 | Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience (✓) | Kresojević, Nikola ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 22M22 |
2021 | Clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion (✓) | Marjanović, Ana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2022 | Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience (✓) | Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2019 | Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons disease (✓) | Radojević, Branislava ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2023 | CYP2C9 screening: important step in siponimod treatment of secondary progressive multiple sclerosis (✓) | Janković, Milena ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2022 | Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans | Maver, Ales; Kovanda, Anja; Bergant, Gaber; Teran, Natasa; Vrecar, Irena; Brankovic, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]()
Racki, Valentino; Vuletic, Vladimira; Peterlin, Borut;
| Conference Paper | Mp. category will be shown later |
2022 | Employment status of patients with Charcot-Marie-Tooth type 1A (✓) | Bjelica, Bogdan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |