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Browsing by Author Marjanović, Ana

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Issue DateTitleAuthor(s)TypeМ-cat.
2019Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriersMarjanovic, Ana  ; Dobricic, Valerija S; Brankovic, M; Jankovic, Milena Z  ; Mandic, Gorana B; Stefanova, Elka D  ; Stevic, Zorica D; Novakovic, Ivana V  ; Kostic, Vladimir SConference Paper
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2023Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian population (✓)Branković, Marija  ; Dragašević, Nataša  ; Svetel, Marina  ; Milovanović, Andona ; Marković, Vladana  ; Janković, Milena  ; Marjanović, Ana  ; Dobričić, Valerija ; Novaković, Ivana  ; Kostić, Vladimir  Conference Paper
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2019Analysis 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
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2017Analysis of mtDNA mutations in Serbian patients with Lebers optic atrophy (✓)Dawod, Phepy G. A.; Rovčanin, Branislav  ; Branković, Marija  ; Marjanović, Ana  ; Janković, Milena  ; Novaković, Ivana  ; Dujmović, Irena ; Jančić, Jasna  ; Kostić, Vladimir  Conference Paper
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2018Analysis of pathogenic mtDNA mutations associated with Leber's hereditary optic neuropathy: our experience (✓)Dawod, Phepy Gamil Anwar; Rovčanin, Branislav  ; Branković, Marija  ; Marjanović, Ana  ; Janković, Milena  ; Novaković, Ivana  ; Motaleb, Fayda Ibrahim Abdel; Jančić, Jasna  ; Kostić, Vladimir  Conference Paper
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2022Analysis of “clinical exome” panel in Serbian patients with cognitive disorders (✓)Branković, Marija  ; Stefanova, Elka  ; Mandić, Gorana  ; Marjanović, Ana  ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Stević, Zorica  ; Janković, Milena  ; Novaković, Ivana  ;
Peterlin, Borut; Kostić, Vladimir  ;
Article
23M23
2019Angiogenin 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
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2023C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia (✓)Marjanović, 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
23M23
2018C9ORF72 genetic screening in Serbian patients with neurodegenerative disordersMarjanovic, Ana  ; Dobricic, Valerija S; Marjanovic, Ivan V; Brankovic, M; Jankovic, Milena Z  ; Mandic, Gorana B; Stevic, Zorica D; Novakovic, Ivana V  ; Stefanova, Elka D  ; Kostic, Vladimir KConference Paper
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2023C9ORF72 intermediate repats in neurodegenerative disorders from Serbia (✓)Marjanović, Ana  ; Branković, Marija  ; Janković, Milena  ; Perić, Stojan ; Dragašević-Mišković, Nataša  ; Mandić, Gorana  ; Ječmenica-Lukić, Milica ; Stanković, Iva ; Stefanova, Elka  ; Stević, Zorica  ;
Novaković, Ivana  ; Svetel, Marina  ; Kostić, Vladimir  ;
Conference Paper
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2022C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population (✓)Marjanović, 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
23M23
2021Clinical and Genetic Analysis of Psychosis in Parkinson’s Disease (✓)Radojević, Branislava; Dragašević-Mišković, Nataša T.  ; Marjanović, Ana  ; Branković, Marija  ; Dobričić, Valerija ; Milovanović, Andona ; Tomić, Aleksandra  ; Svetel, Marina  ; Petrović, Igor  ; Jančić, Ivan  ;
Stanisavljević, Dejana  ; Savić, Miroslav M.  ; Kostić, Vladimir S.  ;
Article
21M21
2023Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience (✓)Kresojević, Nikola ; Perović, Ivana; Stanković, Iva ; Tomić, Aleksandra  ; Ječmenica-Lukić, Milica ; Marković, Vladana  ; Stojković, Tanja  ; Mandić, Gorana  ; Janković, Milena  ; Marjanović, Ana  ;
Branković, Marija  ; Novaković, Ivana  ; Petrović, Igor  ; Dragašević, Nataša  ; Stefanova, Elka  ; Svetel, Marina  ; Kostić, Vladimir  ;
Article
22M22
2021Clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion (✓)Marjanović, Ana  ; Palibrk, Aleksa; Branković, Marija  ; Janković, Milena  ; Dobričić, Valerija ; Novaković, Ivana  ; Stević, Zorica  Conference Paper
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2022Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience (✓)Branković, 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
23M23
2023Clinical phenotype of amyotrophic lateral sclerosis with C9ORF72 repeat expansion in Serbia (✓)Virić, Vanja  ; Palibrk, Aleksa; Marjanović, Ana  ; Božović, Ivo ; Ivanović, Vukan ; Perić, Stojan ; Basta, Ivana  ; Janković, Milena  ; Novaković, Ivana  ; Stević, Zorica  Conference Paper
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2018Contribution to the knowledge on the distribution of freshwater sponges – the Danube and Sava rivers case study (✓)Anđus, Stefan  ; Nikolić, Nađa  ; Dobričić, Valerija ; Marjanović, Ana  ; Gačić, Zoran  ; Branković, Goran  ; Raković, Maja  ; Paunović, Momir  Article
22M22
2019Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons disease (✓)Radojević, Branislava  ; Dragašević-Mišković, Nataša  ; Marjanović, Ana  ; Branković, Marija  ; Dobričić, Valerija ; Milovanović, Andona ; Svetel, Marina  ; Petrović, Igor  ; Savić, Miroslav  ; Jančić, Ivan  ;
Novaković, Ivana  ; Kostić, Vladimir S.  ;
Conference Paper
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2023CYP2C9 screening: important step in siponimod treatment of secondary progressive multiple sclerosis (✓)Janković, Milena  ; Branković, Marija  ; Marjanović, Ana  ; Drulović, Jelena  ; Novaković, Ivana  Conference Paper
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2018Features of the Serbian cohort of patients with calpainopathy (✓)Perić, Stojan ; Kosać, Ana ; Branković, Marija  ; Marjanović, Ana  ; Banko, Bojan  ; Milenković, Sanja  ; Janković, Milena  ; Lavrnić, Dragana  ; Maksimović, Ružica  ; Milić-Rašić, Vedrana  ;
Rakočević-Stojanović, Vidosava  ;
Conference Paper
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