Researchers

Results 241-260 of 392
Issue DateTitleAuthor(s)TypeМp-cat.
2014Clinical and genetic characteristics of dopa-responsive dystonia in a Serbian populationSvetel, Marina V. ; Dobričić, Valerija S. ; Novaković, Ivana V.  ; Dragašević, Nataša T.  ; Petrović, Igor N.  ; Kostić, Vladimir S. Conference Paper
Mp. category will be shown later
2014Executive function and visual memory computerized testing in myotonic dystrophiesPerić, Stojan  ; Stefanova, Elka ; Savić-Pavićević, Dušanka  ; Dobričić, Valerija ; Ralić, Vesna; Pešović, Jovan  ; Novaković, Ivana  ; Rakočević-Stojanović, Vidosava Conference Paper
Mp. category will be shown later
2014Assessment of pain in myotonic dystrophiesPerić, Marina; Perić, Stojan  ; Dobričić Valerija ; Savić-Pavićević, Dušanka  ; Ralić, Vesna; Pešović, Jovan  ; Novaković, Ivana  ; Stojanović, Vidosava Conference Paper
Mp. category will be shown later
2014A novel AMELX mutation in a family with Amelogenesis imperfectaToljić, Boško M.  ; K. Aleksić Babić; V. Dobričić; Novaković, Ivana V.  ; Milašin, Jelena M.  Conference Paper
Mp. category will be shown later
2014Prospective study of perinatal outcome in pregnancies with primary antiphospholipid syndromeĆetković, Aleksandar; Kastratović, Biljana  ; Novaković, Ivana  Article
23M23
2014Novel mutation in human AMELX gene is associated with defect in amelogenesisNovaković, Ivana V.  ; Cvetković, Dragana D.  ; K. Aleksić Babić; Toljić, Boško M.  ; V. Dobričić; Milašin, Jelena M.  Conference Paper
Mp. category will be shown later
2014Prognostic diversity among cytogenetic abnormalities and molecular JAK2V617F marker in primary myelofibrosisĐorđević, V.; Jovanović, J.; Denčić-Fekete, M.; Spasovski, Vesna M.  ; Pavlović, Sonja T.  ; Pavković-Lučić, Sofija  ; Bogdanović, Andrija D.  ; Novaković, Ivana V.  Conference Paper
Mp. category will be shown later
2014657del5 mutation of the NBS1 gene in myelodysplastic syndromeBunjevački, Vera  ; Maksimović, Nela  ; Damnjanović, Tatjana  ; Cvjetićanin, Suzana  ; Novaković, Ivana  ; Luković, Ljiljana ; Ristanović, Momčilo  ; Bogdanović, Andrija  ; Jekić, Biljana  Article
22M22
2014BDNF, COMT and SERT genetic polymorphism combinations and their effect on susceptibility for depression and brain structural connectivityKostić, Milutin  ; E. Canu; A. Munjiza; F. Agosta; Novaković, Ivana  ; V. Dobričić; Miler Jerković, Vera  ; Lečić Toševski, Dušica ; M. FilippiConference Paper
Mp. category will be shown later
2014Altered basal ganglia echogenicity early in sporadic Creutzfeldt-Jakob diseaseVeselinović, Nikola  ; Pavlović, Aleksandra M.  ; Petrović, Boris; Ristić, Aleksandar  ; Novaković, Ivana  ; Švabić-Međedović, Tamara ; Pavlović, Dragan ; Šternić, Nadežda Article
22M22
2014Diagnosis of neuromuscular diseases in Serbia and launch of the Serbian neuromuscular disease network NMD-SERBNETKojić, Snežana  ; Milić-Rašić, Vedrana ; Jelena Mladenović; Ana Kosać; D. Vojinović; J. Nikodinović-Glumac; Stojanović, Vidosava ; Lavrnić, Dragana ; Stević, Zorica ; Basta, Ivana  ;
I. Marjanović; Nikolić, Ana ; Novaković, Ivana  ; Milenković, Sanja  ; Brkušanin, Miloš  ; Pešović, Jovan  ; Savić-Pavićević, Dušanka  ; Stanka Romac; Radojković, Dragica  ; Nestorović, Aleksandra ; Jasnić, Jovana  ; Perić, Stojan  ;
Conference Paper
Mp. category will be shown later
2014Metabolic syndrome in patients with myotonic dystrophy type 1Vujnić, Milorad; Perić, Stojan Z.  ; Dobričić, Valerija S. ; Ralić, Vesna; Novaković, Ivana V.  ; Rakočevic-Stojanović, Vidosava M. Conference Paper
Mp. category will be shown later
2014Possible influence of MTHFR C677T polymorphism on serum lipid levels in Serbian school childrenDamnjanović, Tatjana  ; Luković, Ljiljana ; Cvetković, Dragana  ; Jekić, Biljana  ; Bunjevački, Vera  ; Maksimović, Nela  ; Cvjetićanin, Suzana  ; Majkić-Singh, Nada ; Simeunović, Slavko ; Novaković, Ivana  Article
22M22
2014Three-way interaction of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms and its effect on regional gray matter volume in patients with major depression disorderCanu, Elisa; Kostić, Milutin  ; Munjiza, Ana; Agosta, Federica; Novaković, Ivana  ; Dobričić, Valerija S. ; Miler Jerković, Vera  ; Pekmezović, Tatjana  ; Lečić-Toševski, Dušica ; Filippi, MassimoConference Paper
Mp. category will be shown later
2014Splice site mutation in amelogenin X-linked gene, genotypephenotype relationToljić, Boško M.  ; Lončarić, Darija; Aleksić-Babić, Kristina; Dobričić, Valerija ; Novaković, Ivana V.  ; Milašin, Jelena M.  Conference Paper
Mp. category will be shown later
2014Introduction to molecular genetic diagnosticsNovaković, Ivana  ; Maksimović, Nela  ; Pavlović, Aleksandra  ; Žarković, Milena; Rovčanin, Branislav  ; Mirković, Duško  ; Pekmezović, Tatjana  ; Cvetković, Dragana  Article
23M23
2014Uloga Th17 i Treg ćelija u patogenezi antifosfolipidnog sindromaDragana Popović-Kuzmanović; Novaković, Ivana  ; Stojanović, Ljudmila  ; Zogović, Nevena  ; Tovilović Kovačević, Gordana  ; Trajković, Vladimir  Conference Paper
Mp. category will be shown later
2013Increased activity of interleukin-23/interleukin-17 cytokine axis in primary antiphospholipid syndromePopovic-Kuzmanovic, Dragana; Novaković, Ivana  ; Stojanović, Ljudmila  ; Aksentijevich, Ivona; Zogović, Nevena  ; Tovilović Kovačević, Gordana  ; Trajković, Vladimir  Article
21M21
2013Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilsons disease in SerbiaTomić, Aleksandra  ; Dobricic, Valerija; Novaković, Ivana  ; Svetel, Marina ; Pekmezović, Tatjana  ; Kresojevic, Nikola ; Potrebic, Aleksandra; Kostić, Vladimir Article
23M23
2013A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystoniaSvetel, Marina ; Djuric, Gordana; Novaković, Ivana  ; Dobricic, Valerija; Stefanova, Elka ; Kresojevic, Nikola ; Tomić, Aleksandra  ; Jankovic, Milena ; Petrović, Igor  ; Pekmezović, Tatjana  ;
Kostić, Vladimir ;
Article
23M23