Istraživači
Marjanović, Ana
Резултати 1-20 од 101
| Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
|---|---|---|---|---|
| 2026 | Hidden diagnoses among patients with double seronegative myasthenia gravis![]() | Ivanović, Vukan | Article | 22M22 |
| 2026 | Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy![]() | Ralić, Branislav; Albano, Noemi; Virić, Vanja | Article | 22M22 |
| 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 | Frequency of TREM2 and APOE rare variants in patients with Alzheimer’s disease in Serbia![]() | Stojadinović, Lenka | 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 | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2025 | The pleiotropy of C9orf72 repeat expansions in neurodegenerative diseases![]() | Marjanović, Ana | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | APOE, APP, and PSEN1 mutation screening in Alzheimer’s disease: a 15-year experience in Serbia![]() | Marjanović, Ana | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Genetic and Clinical Insights into ALS/FTD: Profiling a Rare Cohort to Explore Spectrum Heterogeneity![]() | Marjanović, Ana | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2025 | APOE, ATXN1 and ATXN2 genetic analysis in ALS/FTD patients![]() | Marjanović, Ana | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Hereditary neuropathies in Serbian population![]() | Vukojević, Milica | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Chorea in Hereditary Leukodystrophies - Overview of Two Cases![]() | Milovanović, Andona | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2025 | Secondary findings in 443 exome sequencing data![]() | Branković, Marija | Научни чланак | 23M23 - Међународни часопис категорије M23 |
| 2025 | C9orf72–Associated ALS/FTD: From Genetic Diagnosis to Therapeutic Opportunities and Challenges![]() | Marjanović, Ana | Poglavlje u monografiji | Mp kategorija će biti prikazana naknadno. |
| 2025 | Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?![]() | Kresojević, Nikola | Article | 22M22 |
| 2025 | Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy![]() | Ralić, Branislav; Albano, N.; Virić, Vanja | Conference Paper | Mp. category will be shown later |
| 2024 | R47H TREM2 variant among Serbian Alzheimer's disease patients![]() | Andrejić, Nikola | Conference Paper | Mp. category will be shown later |
| 2024 | Secondary findings in 443 whole exome sequencing data![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2024 | NOTCH3 genetic analysis in patients with cerebral small vessel disease![]() | Jovanović, Marija; Vojvodić, Ljubica; Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2024 | APOE genotype, ATXN1 and ATXN2 repeats size in C9orf72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Branković, Marija | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
