Novaković, Ivana

Type

Date issued

392 2000 - 2027
3 1000 - 1999

Mp-cat.

187 М30/М60
48 M21
45 M22
39 M23
17 M21a
15 M10/M40
11 M20/M50
11 other
10 M21a+
4 M24
. next >

Date issued - custom

Year from:

Year to:

Results 121-140 of 395 Results/Page

Issue Date	Title	Author(s)	Type	Мp-cat.
2019	Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers	Marjanović, Ana ; Dobričić, Valerija S. ; Branković, Marija ; Janković, Milena Z. ; Mandić, Gorana B. ; Stefanova, Elka D. ; Stević, Zorica D. ; Novaković, Ivana V. ; Kostić, Vladimir S.	Conference Paper	Mp. category will be shown later
2019	Analisys of the association of TNFα, IL1 β and IL6 promotor gene polymorphisms with the development of severe form of retinopathy of prematurity	Ćućuz, Milica; Pantelić, Jelica; Varljen, Tatjana; Grk, Milka ; Novaković, Ivana ; Damnjanović, Tatjana	Conference Paper	Mp. category will be shown later
2019	Phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia	Perić, Stojan Z. ; Marković, Vladana V. ; De Vriendt, E.; Estrada-Cuzcano, A.; Svetel, Marina V. ; Rakočević-Stojanović, Vidosava M. ; Dragašević-Mišković, Nataša T. ; Stević, Zorica D. ; Božović, Ivo ; Mijajlović, Milija D. ; Mesaroš, Šarlota T. ; Drulović, Jelena S. ; Novaković, Ivana V ; Kostić, Vladimir S. ; Jordanova, A.;	Conference Paper	Mp. category will be shown later
2019	Polymorphisms in PPARG gene: association with obesity-related metabolic traits in a Serbian adolescent population	Pešić, 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	Mp. category will be shown later
2019	Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease	Dopsaj, Violeta ; Topić, Aleksandra ; Savković, Miljan ; Milinković, Neda ; Novaković, Ivana ; Ćujić, Danica ; Simić-Ogrizović, Sanja	Article	21M21
2019	Results of clinical exome analysis in rare neurodegenerative disorders in Serbian population	Branković, 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	Mp. category will be shown later
2019	KRIT1 Gene Analysis In Serbian Patients With Familial Cerebral Cavernous Malformation	Branković, Marija ; Ristić, Aleksandar ; Tamaš, Olivera; Mijajlović, Milija ; Marjanović, Ana ; Andabaka, Marko ; Janković, Milena ; Cvetković, Dragana ; Novaković, Ivana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2019	Phenotypic expression and founder effect of PANK2 c.1583C > T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients	Svetel, Marina ; Hartig, Monika; Cvetković, Dragana ; Beaubois, Cyrielle; Maksić, Jasmina ; Novaković, Ivana ; Krajinović, Maja; Kostić, Vladimir	Article	23M23
2019	Analysis of the association of TNFΑ, IL1Β and IL6 promotor gene polymorphisms with the development of severe form of retinopathy of prematurity	Ćućuz, Milica; Pantelić, Jelica; Varljen, Tatjana; Grk, Milka ; Novaković, Ivana ; Damnjanović, Tatjana M.	Conference Paper	Mp. category will be shown later
2019	Analysis of endothelial nitric oxide synthase T786C gene polymorphism in surgical patients with diffuse secondary peritonitis	Gulić, Milica N. ; Maksimović, Nela S. ; Doklestić, Krstina ; Svirčev, Miloš; Novaković, Ivana	Conference Paper	Mp. category will be shown later
2019	Study of TNF, IL1B, and IL6 genes polymorphisms and susceptibility to bronchopulmonary dysplasia in premature neonates	Damnjanović, Tatjana M. ; Varljen, Tatjana J.; Rakić, Olgica; Jekić, Biljana B. ; Liston, J.; Novaković, Ivana V.	Conference Paper	Mp. category will be shown later
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	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	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 of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients	Vejnović, Dubravka ; Milić, Vera ; Popović, Branka ; Damnjanović, Tatjana ; Maksimović, Nela ; Bunjevački, Vera ; Krajinović, Maja; Novaković, Ivana ; Damjanov, Nemanja ; Jekić, Biljana	Article	21M21
2019	Association of genetic markers of coagulation and fibrinolysis with prematurity complication	Damnjanović, Tatjana M. ; Grk, Milka B. ; Varljen, Tatjana J.; Pantelić, Jelica R.; Maksimović, Nela S. ; Jekić, Biljana B. ; Novaković, Ivana V.	Conference Paper	Mp. category will be shown later
2019	Genetski zasnovana terapija neurodegenerativnih bolesti	Novaković, Ivana ; Svetel, Marina ; Džoljić, Eleonora ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Stefanova, Elka ; Dragašević, Nataša ; Kostić, Vladimir	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	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