Researchers
Dobričić, Valerija
Results 21-40 of 89
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | NOTCH3 mutations in Serbian CADASIL patients![]() | Janković, Milena Z. | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients![]() | Mitropoulos, Konstantinos; ...; Dobričić, Valerija S. | Conference Paper | Mp. category will be shown later |
| 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 |
| 2019 | The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia![]() | Mandić-Stojmenović, Gorana B. | Conference Paper | Mp. category will be shown later |
| 2019 | Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients![]() | Ebrahimi, Keramatollah | Article | 23M23 |
| 2019 | The influence of polymorphisms in COMT, DAT (SLC6A3), DRD2, and ANKK1 genes on the onset of complications of long-term use of levodopa in individuals with Parkinson’s disease![]() | Radojević, Branislava | Conference Paper | Mp. category will be shown later |
| 2019 | Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: First experience![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Results of clinical exome analysis in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2018 | Contribution to the knowledge on the distribution of freshwater sponges – the Danube and Sava rivers case study![]() | Anđus, Stefan | Article | 22M22 |
| 2018 | Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients![]() | Mitropoulos, Konstantinos; ...; Dobričić, Valerija S. | Conference Paper | Mp. category will be shown later |
| 2018 | WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype![]() | Kulikovskaja, Leonora; Sarajlija, Adrijan | Article | Mp. category will be shown later |
| 2018 | Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease![]() | Janković, Milena | Article | 22M22 |
| 2018 | Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease![]() | Janković, Milena Z. | Conference Paper | Mp. category will be shown later |
| 2018 | C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2017 | A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder![]() | Kostić, Milutin | Article | 21M21 |
| 2017 | Next generation sequencing in dystonia - our experience![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2017 | Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients![]() | Mitropoulos, Konstantinos; ...; Dobričić, Valerija | Article | 21M21 |
| 2017 | Study of ATXN2 repeath length in C9ORF72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
