Researchers
Novaković, Ivana
Results 101-120 of 394
| 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 | 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 | 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 | 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 | 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 | 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 | 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 | Genetic Aspects of Inflammation and Immune Response in Stroke | Nikolić, Dejan ; Janković, Milena ; Petrović, Bojana ; Novaković, Ivana | 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 | 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 | 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 association of ADORA(2)A and ADORA(3) 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 | Spectrum of mutations in presenilin 1 gene in patients with early onset Alzheimer disease | Andabaka, Marko ; Branković, Marija ; Marjanović, Ana ; Janković, Milena ; Đuranović, Ana S. ; Grk, Milka ; Novaković, Ivana ; Stefanova, Elka ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2019 | Genetika amiotrofične lateralne skleroze | Stević, Zorica ; Janković, Milena ; Brkušanin, Miloš Đ. ; Keckarević, Dušan P. ; Marjanović, Ana ; Perić, Stojan ; Savić-Pavićević, Dušanka ; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2019 | Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients | Ebrahimi, Keramatollah ; Sabljak, Predrag ; Simić, Aleksandar ; Skrobić, Ognjan ; Veličković, Dejan ; Šljukić, Vladimir; Novaković, Ivana ; Dobričić, Valerija ; Micev, Marjan ; Peško, Predrag | Article | 23M23 |
| 2019 | Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery | Svetel, Marina ; Tomić, Aleksandra ; Dragašević, Nataša ; Petrović, Igor ; Kresojević, Nikola ; Jech, Robert; Urgošik, Dušan; Banjac, Isidora; Vitković, Jelena; Novaković, Ivana ;
Kostić, Vladimir
; | Article | 21M21 |
| 2019 | Molecular genetic testing of Huntington’s disease and genetic counselling | Mandić, Ratka; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Marina Svetel ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2019 | Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients | Vejnović, Dubravka ; Milić, Vera ; Popović, Branka ; Damnjanović, Tatjana ; Maksimović, Nela ; Bunjevački, Vera ; Krajinović, Maja; Novaković, Ivana ; Damjanov, Nemanja ; Jekić, Biljana | Article | 21M21 |
| 2019 | Association of genetic markers of coagulation and fibrinolysis with prematurity complication | Damnjanović, Tatjana M. ; Grk, Milka B. ; Varljen, Tatjana J.; Pantelić, Jelica R.; Maksimović, Nela S. ; Jekić, Biljana B. ; Novaković, Ivana V. | Conference Paper | Mp. category will be shown later |