Researchers

Results 141-160 of 392
Issue DateTitleAuthor(s)TypeМp-cat.
2019Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathyDawod, 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
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2019Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patientsMitropoulos, Konstantinos; ...; Dobričić, Valerija S. ; Novaković, Ivana V.  ; Kostić, Vladimir S. ; ...; (broj koautora 33)Conference Paper
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2019Association between Tumor Necrosis Factor-alpha Promoter-308 G/A Polymorphism and Early Onset Sepsis in Preterm InfantsVarljen, Tatjana; Rakić, Olgica; Sekulović, Gordana; Jekić, Biljana  ; Maksimović, Nela  ; Ranković-Janevski, Milica; Novaković, Ivana  ; Damnjanović, Tatjana  Article
22M22
2019Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infantsMaksimović, Nela S.  ; Varljen, Tatjana; Sekulović, Gordana; Damnjanović, Tatjana M.  ; Novaković, Ivana  Conference Paper
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2019Genetika amiotrofične lateralne sklerozeStević, Zorica ; Janković, Milena ; Brkušanin, Miloš Đ.  ; Keckarević, Dušan P.  ; Marjanović, Ana ; Perić, Stojan  ; Savić-Pavićević, Dušanka  ; Novaković, Ivana  Conference Paper
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2019Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patientsVejnović, Dubravka  ; Milić, Vera ; Popović, Branka  ; Damnjanović, Tatjana  ; Maksimović, Nela  ; Bunjevački, Vera  ; Krajinović, Maja; Novaković, Ivana  ; Damjanov, Nemanja ; Jekić, Biljana  Article
21M21
2019Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patientsEbrahimi, Keramatollah  ; Sabljak, Predrag  ; Simić, Aleksandar  ; Skrobić, Ognjan  ; Veličković, Dejan  ; Šljukić, Vladimir; Novaković, Ivana  ; Dobričić, Valerija ; Micev, Marjan ; Peško, Predrag Article
23M23
2019Spectrum of mutations in presenilin 1 gene in patients with early onset Alzheimer diseaseAndabaka, Marko ; Branković, Marija  ; Marjanović, Ana ; Janković, Milena ; Đuranović, Ana S.  ; Grk, Milka  ; Novaković, Ivana  ; Stefanova, Elka ; Kostić, Vladimir Conference Paper
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2019Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgerySvetel, Marina ; Tomić, Aleksandra  ; Dragašević, Nataša  ; Petrović, Igor  ; Kresojević, Nikola ; Jech, Robert; Urgošik, Dušan; Banjac, Isidora; Vitković, Jelena; Novaković, Ivana  ;
Kostić, Vladimir ;
Article
21M21
2019The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementiaMandić-Stojmenović, Gorana B.  ; Stefanova, Elka D. ; Novaković, Ivana V.  ; Dobričić, Valerija S. ; Stojković, Tanja  ; Kostić, Vladimir K. Conference Paper
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2019Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genesVidmar, Lovro; Maver, Ales; Drulović, Jelena ; Sepčić, Juraj; Novaković, Ivana  ; Ristič, Smiljana; Šega, Saša; Peterlin, BorutArticle
21M21
2019Polymorphisms in PPARG gene: Association with obesity-related metabolic traits in Serbian adolescent populationPešić, Milica M.  ; Maksimović, Nela S.  ; Vidović, Vanja; Vidović, Stojko; Jekić, Biljana B.  ; Damnjanović, Tatjana M.  ; Grk, Milka  ; Dušanović-Pjević, Marija G.  ; Novaković, Ivana  Conference Paper
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2019Molecular genetic testing of Huntington’s disease and genetic counsellingMandić, Ratka; Marjanović, Ana ; Branković, Marija  ; Janković, Milena ; Novaković, Ivana  ; Marina Svetel ; Kostić, Vladimir Conference Paper
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2019Association of genetic markers of coagulation and fibrinolysis with prematurity complicationDamnjanović, Tatjana M.  ; Grk, Milka B.  ; Varljen, Tatjana J.; Pantelić, Jelica R.; Maksimović, Nela S.  ; Jekić, Biljana B.  ; Novaković, Ivana V.  Conference Paper
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2019Genetski zasnovana terapija neurodegenerativnih bolestiNovaković, Ivana  ; Svetel, Marina ; Džoljić, Eleonora  ; Janković, Milena ; Marjanović, Ana ; Branković, Marija  ; Stefanova, Elka ; Dragašević, Nataša  ; Kostić, Vladimir Conference Paper
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2018NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type CBranković, Marija  ; Kresojević, Nikola D. ; Marjanović, Ana ; Novaković, Ivana V.  ; Kostić, Vladimir K. Conference Paper
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2018Identification of mutations in PARK2 gene in Serbian patients with Parkinson's diseaseJanković, Milena Z. ; Dobričić, Valerija S. ; Kresojević, Nikola D. ; Marković, Vladana V.  ; Petrović, Igor N.  ; Svetel, Marina V. ; Pekmezović, Tatjana D.  ; Novaković, Ivana V.  ; Kostić, Vladimir K. Conference Paper
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2018Humana genetika : sveska za praktične radoveLuković, Ljiljana ; Novaković, Ivana  ; Bunjevački, Vera  ; Cvjetićanin, Suzana  ; Damnjanović, Tatjana  ; Jekić, Biljana  ; Perović, Vladimir  ; Bajčetić, Miloš  ; Ristanović, Momčilo  Text book
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2018Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortionHodžić, Alenka; Lavtar, Polona; Ristanović, Momčilo  ; Novaković, Ivana  ; Dotlić, Jelena  ; Peterlin, BorutArticle
21M21
2018Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndromeNovaković, Ivana V.  ; Popović-Kuzmanović, Dragana; Stojanović, Ljudmila  ; Trajković, Vladimir S.  Conference Paper
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