Researchers

Results 121-140 of 395
Issue DateTitleAuthor(s)TypeМp-cat.
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
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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2019Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal DiseaseDopsaj, Violeta ; Topić, Aleksandra  ; Savković, Miljan ; Milinković, Neda  ; Novaković, Ivana  ; Ćujić, Danica  ; Simić-Ogrizović, Sanja Article
21M21
2019Polymorphisms in PPARG gene: association with obesity-related metabolic traits in a Serbian adolescent populationPešić, Milica  ; Maksimović, Nela S.  ; Vidović, Vanja; Vidović, Stojko; Jekić, Biljana B.  ; Damnjanović, Tatjana M.  ; Grk, Milka B.  ; Dušanović-Pjević, Marija G.  ; Novaković, Ivana V.  Conference Paper
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2019Results of clinical exome analysis in rare neurodegenerative disorders in Serbian populationBranković, Marija  ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Svetel, Marina ; Petrović, Igor  ; Perić, Stojan  ; Janković, Milena  ; Marjanović, Ana  ; Stefanova, Elka ;
Novaković, Ivana  ; Peterlin, Borut; Kostić, Vladimir ;
Conference Paper
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2019KRIT1 Gene Analysis In Serbian Patients With Familial Cerebral Cavernous MalformationBranković, Marija  ; Ristić, Aleksandar  ; Tamaš, Olivera; Mijajlović, Milija  ; Marjanović, Ana  ; Andabaka, Marko ; Janković, Milena  ; Cvetković, Dragana  ; Novaković, Ivana  ; Kostić, Vladimir Conference Paper
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2019Analysis of endothelial nitric oxide synthase T786C gene polymorphism in surgical patients with diffuse secondary peritonitisGulić, Milica N. ; Maksimović, Nela S.  ; Doklestić, Krstina  ; Svirčev, Miloš; Novaković, Ivana  Conference Paper
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2019Analysis of the association between ITPA rs1127354 gene polymorphism and efficacy and toxicity of methotrexate in patients with rheumatoid arthritisGrk, 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
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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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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
2019Patofiziologija - 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
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2019The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disordersMarjanović, Ana  ; Dobričić, Valerija ; Branković, Marija  ; Janković, Milena  ; Mandić, Gorana  ; Lukić-Ječmenica, Milica  ; Stefanova, Elka ; Stević, Zorica ; Novaković, Ivana  ; Kostić, Vladimir 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
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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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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2019GLUT1 deficiency syndrome : a case report with a novel SLC2A1mutationIvančević, Nikola  ; Cerovac, Nataša  ; Nikolić, Blažo  ; Čuturilo, Goran  ; Marjanović, Ana  ; Branković, Marija  ; Novaković, Ivana  Article
23M23
2019Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in BelgradeJanković, Milena  ; Marjanovic, Ana  ; Branković, Marija  ; Novaković, Ivana  ; Stević, Zorica 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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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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