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   ; Valerija Dobričić; Milena Janković; Novaković, Ivana ; Comabella M; Drulović, Jelena | Article | 21M21 |
| 2015 | Identification of novel mutations in LRRK2 gene in patients with Parkinson's disease | Jankovic, Milena Z ; Kresojevic, Nikola D ; Dobricic, Valerija S; Markovic, Vladana V ; Petrovic, Igor N; Novakovic, Ivana V ; Kostic, Vladimir S | 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 ; Pekmezović, Tatjana ; Andrić, Sanja ; Mirjanić, Tijana; Novaković, Ivana ; Marić, Nađa | Conference Paper | Mp. category will be shown later |
| 2015 | Varijabilnost multisistemske afekcije u miotoničnoj distrofiji tip 1 - pouke iz srpskog registra (✓) | Rakočević-Stojanović, Vidosava ; Perić, Stojan ; Novaković, Ivana ; Basta, Ivana ; Nikolić, Ana; Dobričić, Valerija ; Kačar, Aleksandra ; Marjanović, Ana ; Savić-Pavićević, Dušanka ; Stević, Zorica ;
Lavrnić, Dragana
; | Conference Paper | Mp. category will be shown later |
| 2015 | Metabolic syndrome in patients with myotonic dystrophy type 1 | Vujnic, Milorad; Perić, Stojan ; Popović, Srđan ; Raseta, Nela; Ralic, Vesna; Dobricic, Valerija; Novakovic, Ivana ; Stojanović, Vidosava | Article | 22M22 |
| 2015 | Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities | Damnjanović, Tatjana ; Čuturilo, Goran ; Maksimović, Nela ; Dimitrijevic N; Jekić, Biljana ; Luković, Ljiljana ; Bunjevački, Vera ; Varljen T; Valerija Dobričić; Jovanovic I;
Kostić, Vladimir
; Novaković, Ivana ; | Article | 23M23 |
| 2015 | Screening for <b><i>C9orf72</i></b> Expansion Mutation in Serbian Patients with Early-Onset Dementia | Mandić-Stojimenović, Gorana ; Stefanova, Elka ; Dobricic, Valerija; Novaković, Ivana ; Stojković, Tanja ; Jesic, Aleksandar; Kostić, Vladimir | Article | 21M21 |
| 2014 | Executive function and visual memory computerized testing in myotonic dystrophies | Perić, Stojan ; Stefanova, Elka ; Savić-Pavićević, Dušanka ; Dobričić Valerija; Ralić Vesna; Pešović, Jovan ; Novaković, Ivana ; Stojanović, Vidosava | 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 ; Westenberger, Ana; Svetel, Marina ; Tomić, Aleksandra ; Ralić, Vesna; Petrović, Igor ; Lukić, Milica Ječmenica ; Lohmann, Katja; Novaković, Ivana ;
Klein, Christine; Kostić, Vladimir
; | Article | 21aM21a |
| 2014 | Neurogenetika u eri 'omika' | Novaković, Ivana ; Dobričić, Valerija; Janković, Milena; Petrović, Igor; Stefanova, Elka; Svetel, Marina ; Kostić, Vladimir | 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 ; Maksić, Jasmina | Conference Paper | Mp. category will be shown later |
| 2014 | Clinical and genetic characteristics of dopa-responsive dystonia in a Serbian population | Svetel, Marina V ; Dobricic, Valerija S; Novakovic, Ivana V ; Dragasevic, Natasa T; Petrovic, Igor N; Kostic, Vladimir S | Conference Paper | Mp. category will be shown later |
| 2014 | Assessment of pain in myotonic dystrophies | Perić M; Perić, Stojan ; Dobričić Valerija; Savić-Pavićević, Dušanka ; Ralić V; Pešović, Jovan ; Novaković, Ivana ; Stojanović, Vidosava | Conference Paper | Mp. category will be shown later |
| 2014 | Inventar supresije misli - Beli medved: validacija srpskog prevoda | Novović, Zdenka ; Ignjatović, Ivana Ignjatović; Dujmović, Andrea Dujmović; Novaković, Ivana | Article | 24M24 |
| 2014 | Clinical and genetic characteristics of dopa-responsive dystonia in Serbian population | Svetel, Marina V ; Dobricic, Valerija S; Novakovic, Ivana V ; Dragasevic, Natasa T; Petrovic, Igor N; Kostic, Vladimir S | Conference Paper | Mp. category will be shown later |
| 2014 | Uloga Th17 i Treg ćelija u patogenezi antifosfolipidnog sindroma (✓) | Dragana Popović-Kuzmanović; Novaković, Ivana ; Stojanović, Ljudmila ; Zogović, Nevena ; Tovilović Kovačević, Gordana ; Trajković, Vladimir | Conference Paper | Mp. category will be shown later |
| 2014 | 657del5 Mutation of the NBS1 Gene in Myelodysplastic Syndrome | Bunjevački, Vera ; Maksimović, Nela ; Damnjanović, Tatjana ; Cvjetićanin, Suzana ; Novaković, Ivana ; Luković, Ljiljana ; Ristanović, Momčilo ; Bogdanović, Andrija ; Jekić, Biljana | Article | 23M23 |
| 2014 | Novel mutation in human AMELX gene is associated with defect in amelogenesis | Novaković, Ivana V. ; Cvetković, Dragana D. ; K. Aleksić Babić; Toljić, Boško M. ; V. Dobričić; Milašin, Jelena M. | 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. ; Pavlović, Sonja T. ; Pavković-Lučić, Sofija ; Bogdanović, Andrija D. ; Novaković, Ivana V. | Conference Paper | Mp. category will be shown later |
| 2014 | A novel AMELX mutation in a family with Amelogenesis imperfecta | Toljić, Boško M. ; K. Aleksić Babić; V. Dobričić; Novaković, Ivana V. ; Milašin, Jelena M. | Conference Paper | Mp. category will be shown later |