Rezultati 1-20 od 89
GodinaNaslovAutor(i)Tip rezultataMp-kat.
2025Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from SerbiaKovačević, Gordana  ; Todorović, Slobodanka ; Novaković, Ivana  ; Dobričić, Valerija ; Savić-Pavićević, Dušanka  ; Milić-Rašić, Vedrana ; Svetel, Marina ; Brkušanin, Miloš  ; Vukomanović, Vladislav  ; Vučinić, Dragana;
Ostojić, Slavica; Putnik, Jovana; Kosać, Ana ;
Naučni članak
21M21 - Vodeći međunarodni časopis kategorije M21
2025Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?Kresojević, Nikola ; Marković, Vladana  ; Geratović, Cveta; Ječmenica-Lukić, Milica  ; Tomić, Aleksandra  ; Dobričić, Valerija ; Stanković, Iva D. ; Stojkovic, Tanja  ; Dragašević, Nataša  ; Šarčević, Maksim;
Jankovic, Milena  ; Marjanovic, Ana ; Novaković, Ivana  ; Kostić, Vladimir ; Svetel, Marina ; Petrović, Igor  ;
Naučni članak
22M22 - Međunarodni časopis kategorije M22
2024Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory CenterStefanova, Elka D. ; Marjanović, Ana ; Dobričić, Valerija S. ; Mandić-Stojmenović, Gorana B.  ; Stojković, Tanja  ; Branković, Marija  ; Šarčević, Maksim; Novaković, Ivana V.  ; Kostić, Vladimir S. Naučni članak
22M22 - Međunarodni časopis kategorije M22
2024Analysis of clinical exome panel in rare movement and cognitive disordersBranković, Marija  ; Dragašević, Nataša  ; Svetel, Marina ; Stefanova, Elka ; Mandić, Gorana  ; Stojković, Tanja  ; Milovanović, Andona ; Marković, Vladana  ; Janković, Milena ; Marjanović, Ana ;
Dobričić, Valerija ; Novaković, Ivana  ; Kostić, Vladimir ;
Konferencijski rad
Mp kategorija će biti prikazana naknadno.
2024C9orf72 genetic screening in patients with ALS/FTD phenotype from SerbiaMarjanović, Ana ; Mandić-Stojmenović, Gorana  ; Milićević, Ognjen  ; Stojković, Tanja  ; Virić, Vanja  ; Janković, Milena ; Branković, Marija  ; Palibrk, Aleksa  ; Ivanović, Vukan ; Dobričić, Valerija ;
Perić, Stojan  ; Novaković, Ivana  ; Stević, Zorica ; Stefanova, Elka ;
Konferencijski rad
Mp kategorija će biti prikazana naknadno.
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 ;
Naučni članak
22M22 - Međunarodni časopis kategorije M22
2023Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian populationBranković, Marija  ; Dragašević, Nataša  ; Svetel, Marina ; Milovanović, Andona ; Marković, Vladana  ; Janković, Milena ; Marjanović, Ana ; Dobričić, Valerija ; Novaković, Ivana  ; Kostić, Vladimir Konferencijski rad
Mp kategorija će biti prikazana naknadno.
2023Motor neuron involvement in facial muscles as characteristic of ANO10 mutationDragašević-Mišović, Nataša  ; Milovanović, Andona ; Stanković, Iva ; Marjanović, Ana ; Branković, Marija  ; Dobričić, Valerija S. ; Petrović, Igor N.  ; Svetel, Marina V. ; Novaković, Ivana  ; Kostić, Vladimir Conference Paper
Mp. category will be shown later
2023Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”Kresojević, Nikola ; Marković, Vladana  ; Dobričić, Valerija ; Stanković, Iva ; Stojković, Tanja  ; Tomić, Aleksandra  ; Ječmenica-Lukić, MIlica  ; Janković, Milena ; Marjanović, Ana ; Branković, Marija  ;
Novaković, Ivana  ; Petrović, Igor  ; Dragašević, Nataša  ; Svetel, Marina ; Kostić, Vladimir ;
Article
21a+M21a+
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
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
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
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
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
2021Clinical and Genetic Analysis of Psychosis in Parkinson’s DiseaseRadojević, 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
2021Selected genetic polymorphisms of COMT, DRD2, ANKK1, and DAT genes and the risk of psychosis in Parkinson's diseaseRadojević, Branislava  ; Dragašević, Nataša T.  ; Milovanović, Andona ; Branković, Marija  ; Svetel, Marina V. ; Dobričić, Valerija S. ; Petrović, Igor N.  ; Savić, Miroslav  ; Stanisavljević, Dejana M.  ; Kostić, Vladimir K. Conference Paper
Mp. category will be shown later
2021Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonismPešić, Milica  ; Dragašević-Mišković, Nataša  ; Marjanović, Ana ; Dobričić, Valerija ; Maksimović, Nela  ; Svetel, Marina ; Perović, Dijana  ; Novaković, Ivana  ; Ćirković, Sanja; Stanković, Iva ;
Kostić, Vladimir ;
Article
22M22
2021Phenotype characteristics of ANO10 mutation carries: a case series from Serbia and a systematic review of the literatureStanković, Iva ; Dragašević, Nataša  ; Milovanović, Andona ; Marjanović, Ana ; Branković, Marija  ; Dobričić, Valerija ; Petrović, Igor  ; Svetel, Marina ; Novaković, Ivana  ; Kostić, Vladimir Conference Paper
Mp. category will be shown later
2020Very Late-Onset Niemann Pick Type C Disease: Example of Progressive Supranuclear Palsy Look-Alike DisorderKresojević, Nikola D. ; Mandić-Stojmenović, Gorana B.  ; Dobričić, Valerija S. ; Petrović, Igor N.  ; Brajković, Leposava D. ; Stefanova, Elka D. ; Svetel, Marina V. ; Kostić, Vladimir K. Article
22M22
2020Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathiesMaksić, Jasmina  ; Dobričić, Valerija ; Rasulić, Lukas  ; Maksimović, Nela  ; Branković, Marija  ; Milić-Rašić, Vedrana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana  Article
23M23