Researchers
Novaković, Ivana
Type
Date issued
- 68 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. |
|---|---|---|---|---|
| 2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy (✓) | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija   ; Marjanović, Ana ; Janković, Milena Z. ; Novaković, Ivana V. ; Dujmović, Irena ; Jančić, Jasna B. ; Kostić, Vladimir S. | Conference Paper | Mp. category will be shown later |
| 2019 | GLUT1 deficiency syndrome : a case report with a novel SLC2A1mutation (✓) | Ivančević, Nikola ; Cerovac, Nataša ; Nikolić, Blažo ; Čuturilo, Goran ; Marjanović, Ana ; Branković, Marija ; Novaković, Ivana | Article | 23M23 |
| 2019 | The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders (✓) | Marjanović, Ana ; Dobričić, Valerija ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Lukić-Ječmenica, Milica ; Stefanova, Elka ; Stević, Zorica ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2019 | Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants | Maksimović, Nela S. ; Varljen Tatjana; Sekulovic Gordana; Damnjanović, Tatjana M. ; Novakovic Ivana | Conference Paper | Mp. category will be shown later |
| 2019 | Association between tumor necrosis factor-α promoter -308 g/a polymorphism and early onset sepsis in preterm infants (✓) | Varljen, Tatjana; Rakić, Olgica; Sekulović, Gordana; Jekić, Biljana ; Maksimović, Nela ; Ranković-Janevski, Milica; Novaković, Ivana ; Damnjanović, Tatjana | Article | 22M22 |
| 2019 | Patofiziologija - mehanizmi poremećaja zdravlja - Deo 1. (✓) | Čemerikić, Dušan; De Luka, Silvio ; Đorđević, Drago ; Marković, Ljiljana ; Milovanović, Ivan; Mladenović, Dušan ; Nedeljkov, Vladimir; Nešović Ostojić, Jelena ; Novaković, Ivana ; Pešić, Branislav Č.;
Radosavljević, Tatjana
; Stanković, Marija ; Todorović, Jasna; Trbović, Aleksandar M.; Vučević, Danijela ; Žunić-Božinovski, Snežana ; | Text book | Mp. category will be shown later |
| 2019 | phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia | Peric, Stojan Z ; Markovic, Vladana V ; De, Vriendt E; Estrada-Cuzcano, A; Svetel, Marina V ; Rakocevic-Stojanovic, Vidosava M; Dragasevic-Miskovic, Natasa T; Stevic, Zorica D; Bozovic, Ivo; Mijajlovic, Milija D ;
Mesaros, Sarlota T; Drulovic, Jelena S
; Novakovic, Ivana V ; Kostic, Vladimir S; Jordanova, A; | 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 ; Dobričić, Valerija ; Svetel, Marina ; Perić, Stojan ; Stefanova, Elka ; Marjanović, Ana ; Petrović, Igor ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2018 | Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease (✓) | Janković, Milena ; Dobričić, Valerija ; Kresojević, Nikola ; Marković, Vladana ; Petrović, Igor ; Svetel, Marina ; Pekmezović, Tatjana ; Novaković, Ivana ; Kostić, Vladimir | Article | 22M22 |
| 2018 | Humana genetika : sveska za praktične radove (✓) | Luković, Ljiljana ; Novaković, Ivana ; Bunjevački, Vera ; Cvjetićanin, Suzana ; Damnjanović, Tatjana ; Jekić, Biljana ; Perović, Vladimir ; Bajčetić, Miloš ; Ristanović, Momčilo | Monograph | Mp. category will be shown later |
| 2018 | Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion (✓) | Hodžić, Alenka; Lavtar, Polona; Ristanović, Momčilo ; Novaković, Ivana ; Dotlić, Jelena ; Peterlin, Borut | Article | 21M21 |
| 2018 | NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C | Brankovic, M; Kresojevic, Nikola D ; Marjanovic, Ana ; Novakovic, Ivana V ; Kostic, Vladimir K | Conference Paper | Mp. category will be shown later |
| 2018 | Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease | Jankovic, Milena Z ; Dobricic, Valerija S; Kresojevic, Nikola D ; Markovic, Vladana V ; Petrovic, Igor N; Svetel, Marina V ; Pekmezovic, Tatjana D ; Novakovic, Ivana V ; Kostic, Vladimir K | Conference Paper | Mp. category will be shown later |
| 2018 | Humana genetika - sveska za praktične radove | Luković, Ljiljana; Novaković, Ivana ; Bunjevački, Vera ; Cvjetićanin, Suzana ; Damnjanović, Tatjana ; Jekić, Biljana ; Perović, Vladimir ; Bajčetić, Miloš ; Ristanović, Momčilo | Text book | |
| 2018 | Neurologija : za studente medicine | Kostić, Vladimir ; Apostolski, Slobodan; Bulat, Petar ; Bumbaširević, Ljiljana ; Cerovac, Nataša ; Dragašević-Mišković, Nataša ; Jančić, Jasna ; Jovanović, Dejana ; Jovanović-Marković, Zagorka; Jović, Nebojša J.;
Kozić, Duško
; Lavrnić, Dragana ; Martinović, Žarko; Milić-Rašić, Vedrana; Drulović, Jelena ; Ocić, Gordana; Pavlović, Dragan M.; Rakočević-Stojanović, Vidosava; Sokić, Dragoslav ; Stefanova, Elka ; Stević, Zorica ; Opinćal-Stošić, Tatjana; Svetel, Marina ; Čovičković-Šternić, Nadežda ; Pavlović, Slobodan; Todorović, Slobodanka; Zidverc, Jasna; Novaković, Ivana ; Vojvodić M., Nikola; Vojvodić, Nikola M.; Mesaroš, Šarlota ; Pavlović, Aleksandra ; Basta, Ivana; Dujmović, Irena; Ristić, Aleksandar; Ercegovac, Marko ; Mijajlović, Milija ; Kačar, Aleksandra ; Petrović, Igor ; Radojičić, Aleksandra; Berisavac, Ivana; Nikolić, Ana; | Text book | Mp. category will be shown later |
| 2018 | Analysis of pathogenic mtDNA mutations associated with Leber's hereditary optic neuropathy: our experience (✓) | Dawod, Phepy Gamil Anwar; Rovčanin, Branislav ; Branković, Marija ; Marjanović, Ana ; Janković, Milena ; Novaković, Ivana ; Motaleb, Fayda Ibrahim Abdel; Jančić, Jasna ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2018 | The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS) | Peterlin, AM; Maver, Ales; Hodzic, A; Sega, S; Drulovic, Jelena S ; Novakovic, Ivana V ; Pekmezovic, Tatjana D ; Ristic, S; Kapovic, M; Peterlin, B | Conference Paper | Mp. category will be shown later |
| 2018 | Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients | Mitropoulos, Konstantinos; ...; Dobricic, Valerija S; Novakovic, Ivana V ; Kostic, Vladimir S; ...; (broj, koautora 30) | Conference Paper | Mp. category will be shown later |
| 2018 | C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders | Marjanovic, Ana ; Dobricic, Valerija S; Marjanovic, Ivan V; Brankovic, M; Jankovic, Milena Z ; Mandic, Gorana B; Stevic, Zorica D; Novakovic, Ivana V ; Stefanova, Elka D ; Kostic, Vladimir K | Conference Paper | Mp. category will be shown later |
| 2018 | Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome | Novakovic, Ivana V ; Popovic-Kuzmanovic, Dragana; Stojanovic, Ljudmila; Trajkovic, Vladimir S | Conference Paper | Mp. category will be shown later |