Researchers
Novaković, Ivana
Type
Date issued
- 67 2020 - 2025
- 214 2010 - 2019
- 62 2000 - 2009
- 3 1990 - 1999
Мп-кат.
- 2 M53
- 1 M51
- 1 M70
- < previous
Date issued - custom
Issue Date | Title | Author(s) | Type | М-cat. |
---|---|---|---|---|
2015 | Are Lebers mitochondial DNA mutations associated with aquaporin-4 autoimmunity? | Dujmovic I; Jančić, Jasna ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21M21 |
2015 | Identification of novel mutations in LRRK2 gene in patients with Parkinson's disease | Jankovic, Milena Z ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2015 | Subclinical psychotic experiences in healthy adults: relationship between genetic variants of FKBP5 gene, neuroticism and childhood trauma (✓) | Mihaljević, Marina ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2015 | Varijabilnost multisistemske afekcije u miotoničnoj distrofiji tip 1 - pouke iz srpskog registra (✓) | Rakočević-Stojanović, Vidosava ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2015 | Metabolic syndrome in patients with myotonic dystrophy type 1 | Vujnic, Milorad; Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() | Article | 22M22 |
2015 | Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities | Damnjanović, Tatjana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 23M23 |
2015 | Screening for <b><i>C9orf72</i></b> Expansion Mutation in Serbian Patients with Early-Onset Dementia | Mandić-Stojimenović, Gorana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21M21 |
2014 | Executive function and visual memory computerized testing in myotonic dystrophies | Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2014 | De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient | Dobričić, Valerija; Kresojević, Nikola ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Article | 21aM21a |
2014 | Neurogenetika u eri 'omika' | Novaković, Ivana ![]() ![]() ![]() ![]() | Book parts | Mp. category will be shown later |
2014 | Primena nove generacije metoda za sekvenciranje dnk (next generation sequencing) u ranoj dijagnostici naslednih poremećaja | Novaković, Ivana ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
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 | Assessment of pain in myotonic dystrophies | Perić M; Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2014 | Inventar supresije misli - Beli medved: validacija srpskog prevoda | Novović, Zdenka ![]() ![]() ![]() ![]() | Article | 24M24 |
2014 | Clinical and genetic characteristics of dopa-responsive dystonia in Serbian population | Svetel, Marina V ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2014 | Uloga Th17 i Treg ćelija u patogenezi antifosfolipidnog sindroma (✓) | Dragana Popović-Kuzmanović; Novaković, Ivana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |
2014 | 657del5 Mutation of the NBS1 Gene in Myelodysplastic Syndrome | Bunjevački, Vera ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | 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 | A novel AMELX mutation in a family with Amelogenesis imperfecta | Toljić, Boško M. ![]() ![]() ![]() ![]() ![]() ![]() | Conference Paper | Mp. category will be shown later |