Researchers
Novaković, Ivana
| Issue Date | Title | Author(s) | Type | М-cat. |
|---|---|---|---|---|
| 2020 | Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegeneration (✓) | Svetel, Marina V.   ; Novakovic, Ivana V. ; Tomić, Svetlana; Kresojević, Nikola D. ; Kostić, Vladimir K. | Article | 23M23 |
| 2020 | Yield of the PMP22 deletion analysis in patients with compression neuropathies (✓) | Ivanović, Vukan ; Branković. Marija ; Bjelica, Bogdan ; Kačar, Aleksandra ; Tubić, Radoje ; Janković, Milena ; Marjanović, Ana ; Novaković, Ivana ; Rakočević-Stojanović, Vidosava ; Perić, Stojan | Article | 21M21 |
| 2020 | Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy (✓) | Dawod, Phepy G. A.; Jančić, Jasna ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Samardžić, Janko ; Potkonjak, Dario ; Đurić, Vesna; Mesaroš, Šarlota ; Novaković, Ivana ;
Abdel Motaleb, Fayda I.; Kostić, Vladimir S.
; Nikolić, Dejan ; | Article | 22M22 |
| 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 M., Nikola; 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 | Recurrent congenital microcephaly: a case report | Komnenic-Radovanovic, Milica; Novakovic, Ivana V ; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Petrovic, Bojana; Kontic-Vucinic, Olivera | 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 | Pesic, Milica ; Maksimovic, Nela S ; Aleksic, Andjelka; Gulic, Milica ; Djuranovic, Ana S ; Grk, Milka B ; Dusanovic-Pjevic, Marija G ; Stankovic, Iva D; Markovic, Vladana V ; Marjanovic, Ana ;
Novakovic, Ivana V
; Dragasevic-Miskovic, Natasa T; Kostic, Vladimir S; | 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 | Gulic, Milica; Maksimovic, Nela S ; Doklestic, Krstina S; Grk, Milka B ; Svircev, M; Dusanovic-Pjevic, Marija G ; Kulic, M; Novakovic, Ivana V | 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 | 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 | Neuropathic pain in patients with Charcot-Marie-Tooth type 1A (✓) | Bjelica, Bogdan ; Perić, Stojan ; Basta, Ivana ; Božović, Ivo ; Kačar, Aleksandra ; Marjanović, Ana ; Ivanović, Vukan ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ;
Rakočević-Stojanović, Vidosava
; | Article | 22M22 |
| 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 |
| 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 | 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 | 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 | 21M21 |
| 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 | 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 | 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 | 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 | 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 |