Novaković, Ivana

Type

Date issued

Mp-cat.

187 М30/М60
47 M21
44 M22
38 M23
17 M21a
15 M10/M40
11 M20/M50
11 other
9 M21a+
4 M24
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Results 101-120 of 391 Results/Page

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	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	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 ;	Article	21M21
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	Article	21M21
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.	Article	23M23
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	Analysis of association of ADORA2A and ADORA3 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
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 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
2019	Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in Belgrade	Janković, Milena ; Marjanovic, Ana ; Branković, Marija ; Novaković, Ivana ; Stević, Zorica	Conference Paper	Mp. category will be shown later
2019	Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy	Dawod, 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	Mp. category will be shown later
2019	Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients	Mitropoulos, Konstantinos; ...; Dobričić, Valerija S. ; Novaković, Ivana V. ; Kostić, Vladimir S. ; ...; (broj koautora 33)	Conference Paper	Mp. category will be shown later
2019	GLUT1 deficiency syndrome : a case report with a novel SLC2A1mutation	Ivančević, Nikola ; Cerovac, Nataša ; Nikolić, Blažo ; Čuturilo, Goran ; Marjanović, Ana ; Branković, Marija ; Novaković, Ivana	Article	23M23
2019	Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants	Maksimović, Nela S. ; Varljen, Tatjana; Sekulović, Gordana; Damnjanović, Tatjana M. ; Novaković, Ivana	Conference Paper	Mp. category will be shown later
2019	Patofiziologija - 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	Mp. category will be shown later
2019	The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders	Marjanović, Ana ; Dobričić, Valerija ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Lukić-Ječmenica, Milica ; Stefanova, Elka ; Stević, Zorica ; Novaković, Ivana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2019	Association between Tumor Necrosis Factor-alpha Promoter-308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants	Varljen, Tatjana; Rakić, Olgica; Sekulović, Gordana; Jekić, Biljana ; Maksimović, Nela ; Ranković-Janevski, Milica; Novaković, Ivana ; Damnjanović, Tatjana	Article	22M22
2019	Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescents	Maksimović, Nela S. ; Vidović, Vanja; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Perović, Dijana ; Vidović, Stojko; Milovac, Irina; Novaković, Ivana V.	Conference Paper	Mp. category will be shown later
2019	Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy	Dawod, 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	Mp. category will be shown later