Istraživači
Novaković, Ivana
Tip
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 2021 | NBIA Syndromes: A Step Forward from the Previous Knowledge (✓) | Svetel, Marina V.   ; Dragašević, Nataša T. ; Petrović, Igor N. ; Novaković, Ivana V. ; Tomić, Aleksandra D. ; Kresojević, Nikola D. ; Stanković, Iva D. ; Kostić, Vladimir K. | Naučni članak | 23M23 - Rad u međ. časopisu |
| 2021 | Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism (✓) | Pešić, Milica ; Dragašević-Mišković, Nataša ; Marjanović, Ana ; Dobričić, Valerija ; Maksimović, Nela ; Svetel, Marina ; Perović, Dijana ; Novaković, Ivana ; Ćirković, Sanja; Stanković, Iva ;
Kostić, Vladimir
; | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
| 2021 | Genetic and epigenomic modifiers of diabetic neuropathy (✓) | Janković, Milena ; Novaković, Ivana ; Nikolić, Dejan ; Mitrović-Maksić, Jasmina ; Branković, Slavko ; Petronić, Ivana ; Ćirović, Dragana ; Dučić, Siniša ; Grajić, Mirko ; Bogićević, Dragana | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
| 2021 | The FKBP5 genotype and childhood trauma effects on FKBP5 DNA methylation in patients with psychosis, their unaffected siblings, and healthy controls (✓) | Mihaljević, Marina ; Franić, Dušanka ; Soldatović, Ivan ; Lukić, Iva ; Andrić-Petrović, Sanja ; Mirjanić, Tijana; Stanković, Biljana ; Žukić, Branka ; Zeljić, Katarina ; Gašić, Vladimir ;
Novaković, Ivana
; Pavlović, Sonja ; Adžić, Miroslav ; Marić, Nađa P. ; | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
| 2021 | Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA (✓) | Đurić, Olivera ; Anđelković, Marina ; Vreća, Miša ; Skakić, Anita ; Pavlović, Sonja ; Novaković, Ivana ; Jovanović, Bojan ; Škodrić-Trifunović, Vesna ; Marković-Denić, Ljiljana | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
| 2021 | Phenotype characteristics of ANO10 mutation carries: a case series from Serbia and a systematic review of the literature (✓) | Stanković, Iva ; Dragašević, Nataša ; Milovanović, Andona ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija ; Petrović, Igor ; Svetel, Marina ; Novaković, Ivana ; Kostić, Vladimir | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2021 | Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis (✓) | Janković, Milena ; Novaković, Ivana ; Gamil Anwar Dawod, Phepy; Gamil Anwar Dawod, Ayman; Drinić, Aleksandra; Abdel Motaleb, Fayda I.; Dučić, Sinisa ; Nikolić, Dejan | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
| 2021 | Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents (✓) | Maksimović, Nela ; Vidović, Vanja; Damnjanović, Tatjana ; Jekić, Biljana ; Majkić-Singh, Nada ; Simeunović, Slavko ; Savić-Božović, Dara; Vidović, Stojko; Novaković, Ivana | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
| 2021 | Clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion (✓) | Marjanović, Ana ; Palibrk, Aleksa; Branković, Marija ; Janković, Milena ; Dobričić, Valerija ; Novaković, Ivana ; Stević, Zorica | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2021 | Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review (✓) | Dawod, Phepy; Jančić, Jasna ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Samardžić, Janko ; Dawod, Ayman Gamil Anwar; Novaković, Ivana ; Abdel Motaleb, Fayda I.; Radlović, Vladimir;
Kostić, Vladimir S.
; Nikolić, Dejan ; | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
| 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 | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
| 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
; | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
| 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. ; | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2020 | Recurrent congenital microcephaly: a case report | Komnenic-Radovanovic, Milica; Novakovic, Ivana V ; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Petrovic, Bojana; Kontic-Vucinic, Olivera | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 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; | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 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 | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 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 ; | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
| 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 | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
| 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. | Naučni članak | 23M23 - Rad u međ. časopisu |
| 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; | Udžbenik | Mp kategorija će biti prikazana naknadno. |