Researchers
Dobričić, Valerija
Results 41-60 of 89
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder![]() | Kostić, Milutin | Article | 21M21 |
| 2017 | PANK2 gene mutation spectrum in Serbian patients with neurodegeneration with brain iron accumulation![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2017 | The presence of premutation in the FMR1 gene in patients with clinical picture of degenerative ataxia, tremor and parkinsonism![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2017 | Transcranial sonography in dopa-responsive dystonia![]() | Svetel, Marina | Article | 21M21 |
| 2017 | The Signature of Trauma in Psychosis: A Preliminary Genetic and Epigenetic Analyses of FK506-Binding Protein 5 Regulation![]() | Marić-Bojović, Nađa | Conference Paper | Mp. category will be shown later |
| 2017 | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia![]() | Dobričić, Valerija | Article | 21aM21a |
| 2017 | Genotype-phenotype correlation in Friedreich's ataxia![]() | Kovačević, G.; Todorović, S.; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2016 | Five-year study of quality of life in myotonic dystrophy![]() | Perić, Stojan | Article | 21M21 |
| 2016 | Genetic mutations in Frontemporal dementia - report from the memory clinic from Serbia![]() | Stefanova, Elka D. | Conference Paper | Mp. category will be shown later |
| 2016 | Prospective study of disease progression in atypical form of pantothenate-kinase-associated neurodegeneration (PKAN)![]() | Tomić, Aleksandra D. | Conference Paper | Mp. category will be shown later |
| 2016 | Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking![]() | Radovanović, Saša M. | Article | 21aM21a |
| 2016 | HPCA-related dystonia: Too rare to be found?![]() | Dobričić, Valerija | Article | 21aM21a |
| 2016 | Clusters of cognitive impairment among different forms of myotonic dystrophies![]() | Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2016 | Varijabilnost u naslednoj osnovi čoveka : značaj i primena u studijama asocijacije i u dijagnostici![]() | Novaković, Ivana | Book parts | Mp. category will be shown later |
| 2016 | Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia![]() | Dragašević-Mišković, Nataša | Contribution to periodical | 21aM21a |
| 2015 | Mreža za neuromišićne bolesti Srbije (NMD-SerbNet)![]() | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | Variability of multisystemic features in myotonic dystrophy type 1 – lessons from Serbian registry![]() | Rakočević-Stojanović, Vidosava | Article | 22M22 |
| 2015 | Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited![]() | Dobričić, Valerija | Article | 21M21 |
