Researchers

Results 101-120 of 391
Issue DateTitleAuthor(s)TypeМp-cat.
2020Recurrent congenital microcephaly: a case reportKomnenić-Radovanović, Milica ; Novaković, Ivana V.  ; Čuturilo, Goran  ; Ruml-Stojanović, Jelena ; Petrović, Bojana ; Kontić-Vučinić, Olivera  Conference Paper
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2020Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1ABjelica, 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
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2020Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic NeuropathyDawod, 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
21M21
2020Yield of the PMP22 deletion analysis in patients with compression neuropathiesIvanović, Vukan ; Branković. Marija  ; Bjelica, Bogdan ; Kačar, Aleksandra  ; Tubić, Radoje  ; Janković, Milena ; Marjanović, Ana ; Novaković, Ivana  ; Rakočević-Stojanović, Vidosava ; Perić, Stojan  Article
21M21
2020Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegenerationSvetel, Marina V. ; Novakovic, Ivana V.  ; Tomić, Svetlana; Kresojević, Nikola D. ; Kostić, Vladimir K. Article
23M23
2020Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathiesMaksić, Jasmina  ; Dobričić, Valerija ; Rasulić, Lukas  ; Maksimović, Nela  ; Branković, Marija  ; Milić-Rašić, Vedrana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana  Article
23M23
2020Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritisGrk, Milka  ; Milic, Vera ; Dolzan, Vita; Maksimović, Nela  ; Damnjanović, Tatjana  ; Dušanović-Pjević, Marija  ; Pešić, Milica  ; Novaković, Ivana  ; Jekić, Biljana  Article
21M21
2020Association of the brain-derived neurotrophic factor Val66Met polymorphism with body mass index, fasting glucose levels and lipid status in adolescentsVidović, Vanja; Maksimović, Nela  ; Novaković, Ivana  ; Damnjanović, Tatjana  ; Jekić, Biljana  ; Vidović, Stojko; Majkić-Singh, Nada ; Stamenković-Radak, Marina  ; Nikolić, Dejan  ; Marisavljević, Dragomir  Article
23M23
2020Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentationJančić, Jasna B.  ; Rovčanin, Branislav R.; Đurić, Vesna; Pepić, Ana; Samardžić, Janko S.  ; Nikolić, Blažo  ; Novaković, Ivana V.  ; Kostić, Vladimir S. Article
21M21
2020In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathyRovčanin, Branislav R.  ; Jančić, Jasna B.  ; Samardžić, Janko M.  ; Rovčanin, Marija G.  ; Nikolić, Blažo  ; Ivančević, Nikola  ; Novaković, Ivana V.  ; Kostić, Vladimir K. Article
21aM21a
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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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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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
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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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 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
2019Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescentsMaksimović, Nela S.  ; Vidović, Vanja; Damnjanović, Tatjana M.  ; Jekić, Biljana B.  ; Perović, Dijana  ; Vidović, Stojko; Milovac, Irina; Novaković, Ivana V.  Conference Paper
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2019Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathyDawod, Phepy G. A.; Rovčanin, Branislav R.  ; Branković, Marija  ; Marjanović, Ana ; Janković, Milena Z. ; Novaković, Ivana V.  ; Motaleb, Abdel F.; Jančić, Jasna B.  ; Kostić, Vladimir S. Conference Paper
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