Researchers
Novaković, Ivana
Results 241-260 of 392
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2014 | Clinical and genetic characteristics of dopa-responsive dystonia in a Serbian population![]() | Svetel, Marina V. | Conference Paper | Mp. category will be shown later |
| 2014 | Executive function and visual memory computerized testing in myotonic dystrophies![]() | Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2014 | Assessment of pain in myotonic dystrophies![]() | Perić, Marina; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2014 | A novel AMELX mutation in a family with Amelogenesis imperfecta | Toljić, Boško M. | Conference Paper | Mp. category will be shown later |
| 2014 | Prospective study of perinatal outcome in pregnancies with primary antiphospholipid syndrome![]() | Ćetković, Aleksandar; Kastratović, Biljana | Article | 23M23 |
| 2014 | Novel mutation in human AMELX gene is associated with defect in amelogenesis | Novaković, Ivana V. | Conference Paper | Mp. category will be shown later |
| 2014 | Prognostic diversity among cytogenetic abnormalities and molecular JAK2V617F marker in primary myelofibrosis | Đorđević, V.; Jovanović, J.; Denčić-Fekete, M.; Spasovski, Vesna M. | Conference Paper | Mp. category will be shown later |
| 2014 | 657del5 mutation of the NBS1 gene in myelodysplastic syndrome![]() | Bunjevački, Vera | Article | 22M22 |
| 2014 | BDNF, COMT and SERT genetic polymorphism combinations and their effect on susceptibility for depression and brain structural connectivity | Kostić, Milutin | Conference Paper | Mp. category will be shown later |
| 2014 | Altered basal ganglia echogenicity early in sporadic Creutzfeldt-Jakob disease![]() | Veselinović, Nikola | Article | 22M22 |
| 2014 | Diagnosis of neuromuscular diseases in Serbia and launch of the Serbian neuromuscular disease network NMD-SERBNET | Kojić, Snežana | Conference Paper | Mp. category will be shown later |
| 2014 | Metabolic syndrome in patients with myotonic dystrophy type 1![]() | Vujnić, Milorad; Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2014 | Possible influence of MTHFR C677T polymorphism on serum lipid levels in Serbian school children![]() | Damnjanović, Tatjana | Article | 22M22 |
| 2014 | Three-way interaction of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms and its effect on regional gray matter volume in patients with major depression disorder![]() | Canu, Elisa; Kostić, Milutin | Conference Paper | Mp. category will be shown later |
| 2014 | Splice site mutation in amelogenin X-linked gene, genotypephenotype relation![]() | Toljić, Boško M. | Conference Paper | Mp. category will be shown later |
| 2014 | Introduction to molecular genetic diagnostics![]() | Novaković, Ivana | Article | 23M23 |
| 2014 | Uloga Th17 i Treg ćelija u patogenezi antifosfolipidnog sindroma![]() | Dragana Popović-Kuzmanović; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2013 | Increased activity of interleukin-23/interleukin-17 cytokine axis in primary antiphospholipid syndrome | Popovic-Kuzmanovic, Dragana; Novaković, Ivana | Article | 21M21 |
| 2013 | Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilsons disease in Serbia | Tomić, Aleksandra | Article | 23M23 |
| 2013 | A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia | Svetel, Marina | Article | 23M23 |
