Researchers
Dragašević Mišković, Nataša
Results 1-20 of 139
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease![]() | Bergant, Gaber; ...; Branković, Marija
...; (broj koautora 19);
| Article | 22M22 |
| 2025 | Examination of the frequency and characteristics of impulse control disorders in Wilson's disease![]() | Nikolić, A.; Marković, Vladana | Conference Paper | Mp. category will be shown later |
| 2025 | The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson's disease![]() | Radojević, Branislava | Article | 22M22 |
| 2025 | Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease![]() | Kovanda, Anja; Šušmelj, Lara; Jaklič, Helena; Lukežič, Tadeja; Maver, Aleš; Petrović, Igor N. | Contribution to periodical | 22M22 |
| 2025 | Chorea in Hereditary Leukodystrophies - Overview of Two Cases![]() | Milovanović, Andona | Article | 22M22 |
| 2025 | An Unusual Presentation of a DNMT1 Mutation: Progressive Supranuclear Palsy Look-Alike Disorder![]() | Ječmenica-Lukić, Milica V. | Article | 21M21 |
| 2025 | Clinical exome sequencing identifies pathogenic SQSTM1 variant in a patient with chorea and gaze palsy![]() | Stojadinović, Lenka | Conference Paper | Mp. category will be shown later |
| 2025 | Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?![]() | Kresojević, Nikola | Article | 22M22 |
| 2024 | RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia![]() | Milovanović, Andona | Article | 21M21 |
| 2024 | Distonija-ataksija sindrom ranog početka kao manifestacija POLR3a povezane leukodistrofije![]() | Šarčević, Maksim; Milovanović, Andona | Conference Paper | Mp. category will be shown later |
| 2024 | Osnovi neurološkog pregleda![]() | Kostić, Vladimir | Text book | Mp. category will be shown later |
| 2024 | The Impact of Demographic and Clinical Factors on the Quality of Life in Patients with Neurodegenerative Cerebellar Ataxias![]() | Tamaš, Olivera S.; Marić, Gorica D. | Article | 22M22 |
| 2024 | Structural brain heterogeneity underlying symptomatic and asymptomatic genetic dystonia: a multimodal MRI study![]() | Tomić, Aleksandra D. | Article | 21aM21a |
| 2024 | Sleep problems in female carriers of premutation in the FMR1 gene![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2024 | Motor imagery ability in patients with functional dystonia![]() | Tomić, Aleksandra | Article | 21M21 |
| 2024 | Analysis of clinical exome panel in rare movement and cognitive disorders![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2024 | Transcranial Sonography Characteristics of Cerebellar Neurodegenerative Ataxias![]() | Tamaš, Olivera S.; Mijajlović, Milija D. | Article | 22M22 |
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series![]() | Milovanović, Andona | Article | 21a+M21a+ |
| 2024 | Wilson’s disease![]() | Svetel, Marina | Article | 23M23 |
| 2024 | Patterns of neuropsychiatric symptoms in primary and secondary tauopathies: Caregiver and patient perspectives![]() | Ječmenica-Lukić, Milica | Article | 53M53 |
