Researchers



Results 41-60 of 107
Issue DateTitleAuthor(s)TypeМp-cat.
2023CYP2C9 screening: important step in siponimod treatment of secondary progressive multiple sclerosisJanković, Milena ; Branković, Marija  ; Marjanović, Ana ; Drulović, Jelena ; Novaković, Ivana  Conference Paper
Mp. category will be shown later
2023Clinical phenotype of amyotrophic lateral sclerosis with C9ORF72 repeat expansion in SerbiaVirić, Vanja  ; Palibrk, Aleksa; Marjanović, Ana ; Božović, Ivo ; Ivanović, Vukan ; Perić, Stojan  ; Basta, Ivana  ; Janković, Milena ; Novaković, Ivana  ; Stević, Zorica Conference Paper
Mp. category will be shown later
2023Sepsis in Neurology Intensive Care Unit Incidence and OutcomeIvanović, Jovana B. ; Ždraljević, Mirjana; Radišić, Vanja ; Đurđević, Katarina  ; Janković, Milena Z. ; Švabić, Tamara S ; Pađen, Višnja; Jovanović, Dejana R.  ; Berisavac, Ivana I.  Conference Paper
Mp. category will be shown later
2023C9orf72 genetic screening in amyotrophic lateral sclerosis patients from SerbiaMarjanović, Ana ; Palibrk, Aleksa; Dobričić, Valerija ; Milićević, Ognjen  ; Branković, Marija  ; Virić, Vanja  ; Drinić, Aleksandra; Mandić-Stojmenović, Gorana  ; Janković, Milena ; Basta, Ivana  ;
Perić, Stojan  ; Novaković, Ivana  ; Stefanova, Elka ; Stević, Zorica ;
Article
22M22
2022A multicenter study of genetic testing for Parkinson’s disease in the clinical settingKovanda, Anja; Rački, Valentino; Bergant, Gaber; Georgiev, Dejan; Flisar, Dušan; Papić, Eliša; Branković, Marija  ; Janković, Milena ; Svetel, Marina ; Teran, Nataša;
Maver, Aleš; Kostić, Vladimir S. ; Novaković, Ivana  ; Pirtošek, Zvezdan; Rakuša, Martin; Vuletić, Vladimira; Peterlin, Borut;
Article
21aM21a
2022Analysis of “clinical exome” panel in Serbian patients with cognitive disordersBranković, Marija  ; Stefanova, Elka ; Mandić, Gorana  ; Marjanović, Ana ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Stević, Zorica ; Janković, Milena ; Novaković, Ivana  ;
Peterlin, Borut; Kostić, Vladimir ;
Article
22M22
2022The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic OptionsJanković, Milena ; Petrović, Bojana ; Novaković, Ivana  ; Branković, Slavko  ; Radosavljević, Nataša ; Nikolić, Dejan  Article
21M21
2022C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian populationMarjanović, Ana ; Dobričić, Valerija ; Ječmenica-Lukić, Milica  ; Stanković, Iva ; Milićević, Ognjen  ; Dragašević-Mišković, Nataša  ; Branković, Marija  ; Janković, Milena ; Novaković, Ivana  ; Svetel, Marina ;
Stefanova, Elka ; Kostić, Vladimir ;
Article
22M22
2022Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experienceKresojević, Nikola ; Dobričić, Valerija ; Ječmenica-Lukić, Milica  ; Tomić, Aleksandra  ; Petrović, Igor  ; Dragašević, Nataša  ; Perović, Ivana; Marjanović, Ana ; Branković, Marija  ; Janković, Milena ;
Novaković, Ivana  ; Svetel, Marina ; Kostić, Vladimir S. ;
Article
21aM21a
2022Clinical exome sequencing in Serbian patients with movement disorders – Single centre experienceBranković, Marija  ; Dragašević, Nataša  ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Petrović, Igor  ; Perić, Stojan  ; Marjanović, Ana ; Janković, Milena ; Jančić, Jasna  ;
Novaković, Ivana  ; Peterlin, Borut; Svetel, Marina ; Kostić, Vladimir ;
Article
22M22
2022Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the BalkansMaver, Aleš; Kovanda, Anja; Bergant, Gaber; Teran, Nataša; Vrečar, Irena; Branković, Marija  ; Janković, Milena Z. ; Svetel, Marina V. ; Kostić, Vladimir S. ; Novaković, Ivana V.  ;
Rački, Valentino; Vuletić, Vladimira; Peterlin, Borut;
Conference Paper
Mp. category will be shown later
2021Novel TEAD1 gene variant in a Serbian family with Sveinsson's chorioretinal atrophyGrubiša, Ivana  ; Janković, Milena ; Nikolić, Nađa  ; Jakšić, Vesna Z.  ; Risimić, Dijana  ; Mavija, Milka; Stamenković, Miroslav R.  ; Zlatović, Mario  ; Milašin, Jelena  Article
21aM21a
2021Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral SclerosisJanković, Milena ; Novaković, Ivana  ; Gamil Anwar Dawod, Phepy; Gamil Anwar Dawod, Ayman; Drinić, Aleksandra; Abdel Motaleb, Fayda I.; Dučić, Sinisa  ; Nikolić, Dejan  Article
21M21
2021Early predictors of mortality in patients with metabolic encephalopathyĐurđević, Katarina; Arsenijević, Mirjana; Radišić, Vanja ; Janković, Milena Z. ; Ercegovac, Marko D.  ; Jovanović, Dejana R.  ; Berisavac, Ivana I.  Conference Paper
Mp. category will be shown later
2021Guillain-Barre Syndrome during pregnancy: case seriesArsenijević, Mirjana; Radišić, Vanja ; Janković, Milena Z. ; Perić, Stojan Z.  ; Jovanović, Dejana R.  ; Berisavac, Ivana I.  Conference Paper
Mp. category will be shown later
2021Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot–Marie–Tooth disease type 1ABjelica, Bogdan ; Perić, Stojan  ; Božović, Ivo ; Janković, Milena ; Branković, Marija  ; Palibrk, Aleksa; Rakočević-Stojanović, Vidosava Article
22M22
2021Genetic and epigenomic modifiers of diabetic neuropathyJanković, Milena ; Novaković, Ivana  ; Nikolić, Dejan  ; Mitrović-Maksić, Jasmina  ; Branković, Slavko  ; Petronić, Ivana ; Ćirović, Dragana  ; Dučić, Siniša  ; Grajić, Mirko  ; Bogićević, DraganaArticle
21M21
2021The impact of ACA occlusion on the short-term functional outcome of patients treated with mechanical thrombectomyJankovic, Milena ; Arsenijević, Mirjana; Vukašinović, Ivan ; Stanarčević, Predrag; Švabić-Međedović, Tamara ; Pađen, Višnja ; Budimkić-Stefanović, Maja ; Berisavac, Ivana  ; Ercegovac, Marko  ; Nestorović, Dragoslav ;
Cvetić, Vladimir; Vitošević, Filip  ; Nedeljković, Žarko; Jovanović, Dejana R.  ;
Conference Paper
Mp. category will be shown later
2021Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature ReviewDawod, Phepy; Jančić, Jasna  ; Marjanović, Ana ; Branković, Marija  ; Janković, Milena ; Samardžić, Janko  ; Dawod, Ayman Gamil Anwar; Novaković, Ivana  ; Abdel Motaleb, Fayda I.; Radlović, Vladimir;
Kostić, Vladimir S. ; Nikolić, Dejan  ;
Article
21M21
2021Clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansionMarjanović, Ana ; Palibrk, Aleksa; Branković, Marija  ; Janković, Milena ; Dobričić, Valerija ; Novaković, Ivana  ; Stević, Zorica Conference Paper
Mp. category will be shown later