Researchers
Marjanović, Ana
Results 41-60 of 101
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients![]() | Pešić, Milica | 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 | 22M22 |
| 2022 | Analysis of “clinical exome” panel in Serbian patients with cognitive disorders![]() | Branković, Marija | Article | 22M22 |
| 2022 | Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience![]() | Branković, Marija | Article | 22M22 |
| 2022 | Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience![]() | Kresojević, Nikola | Article | 21aM21a |
| 2022 | The correlation between genetic factors and freezing of gait in patients with Parkinson's disease![]() | Radojević, Branislava; Dragašević-Mišković, Nataša | Article | 21M21 |
| 2021 | Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism![]() | Pešić, Milica | Article | 22M22 |
| 2021 | Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review![]() | Dawod, Phepy; Jančić, Jasna | Article | 21M21 |
| 2021 | Clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion![]() | Marjanović, Ana | 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. | Article | 21M21 |
| 2021 | Spodbude in naložbe v primarnem proizvodnem sektorju med globalno pandemijo![]() | Petrović, Vesna | Conference Paper | Mp. category will be shown later |
| 2021 | Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit![]() | Miletić, Aleksandra; Ruml-Stojanović, Jelena | Article | 21aM21a |
| 2021 | Phenotype characteristics of ANO10 mutation carries: a case series from Serbia and a systematic review of the literature![]() | Stanković, Iva | Conference Paper | Mp. category will be shown later |
| 2020 | Neuropathic pain in patients with Charcot-Marie-Tooth type 1A![]() | Bjelica, Bogdan | Article | 22M22 |
| 2020 | The influence of ANNK1/DRD2 haplotypes on the onset of complications of long-term levodopa therapy in Parkinson's disease![]() | Radojević, Branislava | Conference Paper | Mp. category will be shown later |
| 2020 | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1β, andTNF-α in relation with Parkinson’s disease progression![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2020 | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2020 | Yield of the PMP22 deletion analysis in patients with compression neuropathies![]() | Ivanović, Vukan | Article | 21M21 |
| 2020 | Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy![]() | Dawod, Phepy G. A.; Jančić, Jasna | Article | 21M21 |
| 2019 | NOTCH3 mutations in Serbian CADASIL patients![]() | Janković, Milena Z. | Conference Paper | Mp. category will be shown later |
