Researchers
Novaković, Ivana
Results 101-120 of 392
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2020 | Recurrent congenital microcephaly: a case report | Komnenić-Radovanović, Milica  ; Novaković, Ivana V.  ; Čuturilo, Goran ; Ruml-Stojanović, Jelena ; Petrović, Bojana ; Kontić-Vučinić, Olivera | Conference Paper | Mp. category will be shown later |
| 2020 | Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A | Bjelica, Bogdan ; Perić, Stojan Z. ; Božović, Ivo ; Basta, Ivana Z. ; Kačar, Aleksandra S. ; Janković, Milena Z. ; Branković, Marija ; Palibrk, Aleksa ; Novaković, Ivana V. ; Lavrnić, Dragana V. ;
Stević, Zorica D.
; Rakočević-Stojanović, Vidosava M. ; | Conference Paper | Mp. category will be shown later |
| 2020 | Influence of eNOS gene haplotypes and iNOS rs2297518 gene variant on severe complications and mortality in surgical patients with secondary peritonitis | Gulić, Milica ; Maksimović, Nela S. ; Doklestić, Krstina S. ; Grk, Milka B. ; Svirčev, Miloš; Dušanović-Pjević, Marija G. ; Kulić, M.; Novaković, Ivana V | Conference Paper | Mp. category will be shown later |
| 2020 | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression | Pešić, Milica ; Maksimović, Nela S. ; Aleksić, Anđelka; Gulić, Milica ; Đuranović, Ana S. ; Grk, Milka B. ; Dušanović-Pjević, Marija G. ; Stanković, Iva D. ; Marković, Vladana V. ; Marjanović, Ana ;
Novaković, Ivana V.
; Dragašević-Mišković, Nataša T. ; Kostić, Vladimir S. ; | Conference Paper | Mp. category will be shown later |
| 2020 | Neurologija : za studente medicine | Kostić, Vladimir ; Apostolski, Slobodan ; Bulat, Petar ; Bumbaširević, Ljiljana ; Cerovac-Ćosić, 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 ; Stošić-Opinćal, Tatjana ; Svetel, Marina ; Čovičković-Šternić, Nadežda ; Pavlović, Slobodan; Todorović, Slobodanka ; Zidverc Trajković, Jasna ; Novaković, Ivana ; Vojvodić, Nikola M. ; Mesaroš, Šarlota ; Pavlović, Aleksandra ; Basta, Ivana ; Dujmović Bašuroski, 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 |
| 2020 | Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants | Varljen, Tatjana; Sekulović, Gordana; Rakić, Olgica; Maksimović, Nela ; Jekić, Biljana ; Novaković, Ivana ; Damnjanović, Tatjana | Article | 22M22 |
| 2020 | Association of the brain-derived neurotrophic factor Val66Met polymorphism with body mass index, fasting glucose levels and lipid status in adolescents | Vidović, Vanja; Maksimović, Nela ; Novaković, Ivana ; Damnjanović, Tatjana ; Jekić, Biljana ; Vidović, Stojko; Majkić-Singh, Nada ; Stamenković-Radak, Marina ; Nikolić, Dejan ; Marisavljević, Dragomir | Article | 23M23 |
| 2020 | Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation | Jančić, Jasna B. ; Rovčanin, Branislav R.; Đurić, Vesna; Pepić, Ana; Samardžić, Janko S. ; Nikolić, Blažo ; Novaković, Ivana V. ; Kostić, Vladimir S. | Article | 21M21 |
| 2020 | In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathy | Rovčanin, Branislav R. ; Jančić, Jasna B. ; Samardžić, Janko M. ; Rovčanin, Marija G. ; Nikolić, Blažo ; Ivančević, Nikola ; Novaković, Ivana V. ; Kostić, Vladimir K. | Article | 21aM21a |
| 2020 | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies | Maksić, Jasmina ; Dobričić, Valerija ; Rasulić, Lukas ; Maksimović, Nela ; Branković, Marija ; Milić-Rašić, Vedrana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana | Article | 23M23 |
| 2020 | Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis | Grk, Milka ; Milic, Vera ; Dolzan, Vita; Maksimović, Nela ; Damnjanović, Tatjana ; Dušanović-Pjević, Marija ; Pešić, Milica ; Novaković, Ivana ; Jekić, Biljana | Article | 21M21 |
| 2019 | Analysis of the association between ITPA rs1127354 gene polymorphism and efficacy and toxicity of methotrexate in patients with rheumatoid arthritis | Grk, Milka ; Milić, Vera ; Maksimović, Nela S. ; Damnjanović, Tatjana M. ; Dušanović-Pjević, Marija ; Pešić, Milica ; Novaković, Ivana ; Andabaka, Marko ; Đuranović, Ana S. ; Jekić, Biljana B. | Conference Paper | Mp. category will be shown later |
| 2019 | Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescents | Maksimović, Nela S. ; Vidović, Vanja; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Perović, Dijana ; Vidović, Stojko; Milovac, Irina; Novaković, Ivana V. | Conference Paper | Mp. category will be shown later |
| 2019 | Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy | Dawod, Phepy G. A.; Rovčanin, Branislav R. ; Branković, Marija ; Marjanović, Ana ; Janković, Milena Z. ; Novaković, Ivana V. ; Motaleb, Abdel F.; Jančić, Jasna B. ; Kostić, Vladimir S. | Conference Paper | Mp. category will be shown later |
| 2019 | Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons disease | Radojević, Branislava ; Dragašević-Mišković, Nataša ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija ; Milovanović, Andona ; Svetel, Marina ; Petrović, Igor ; Savić, Miroslav ; Jančić, Ivan ;
Novaković, Ivana
; 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 | Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in Belgrade | Janković, Milena ; Marjanovic, Ana ; Branković, Marija ; Novaković, Ivana ; Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 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 | Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients | Mitropoulos, Konstantinos; ...; Dobričić, Valerija S. ; Novaković, Ivana V. ; Kostić, Vladimir S. ; ...; (broj koautora 33) | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers | Marjanović, Ana ; Dobričić, Valerija S. ; Branković, Marija ; Janković, Milena Z. ; Mandić, Gorana B. ; Stefanova, Elka D. ; Stević, Zorica D. ; Novaković, Ivana V. ; Kostić, Vladimir S. | Conference Paper | Mp. category will be shown later |