Researchers
Branković, Marija
Results 41-60 of 93
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2022 | Physical and Mental Aspects of Quality of Life in Patients With Charcot-Marie-Tooth Disease Type 1A | Ivanović, Vukan  ; Bjelica, Bogdan ; Palibrk, Aleksa; Branković, Marija  ; Božović, Ivo ; Basta, Ivana ; Savić, Andrija; Rakočević-Stojanović, Vidosava ; Kačar, Aleksandra | Article | 21M21 |
| 2022 | A multicenter study of genetic testing for Parkinson’s disease in the clinical setting | Kovanda, 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 |
| 2022 | Analysis 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 | 22M22 |
| 2022 | C9ORF72 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 | 22M22 |
| 2022 | Employment status of patients with Charcot-Marie-Tooth type 1A | Bjelica, Bogdan ; Branković, Marija ; Božović, Ivo ; Palibrk, Aleksa; Kačar, Aleksandra ; Rakočević-Stojanović, Vidosava | Article | 22M22 |
| 2022 | Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience | Kresojević, 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 |
| 2022 | Clinical 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 | 22M22 |
| 2022 | Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans | Maver, 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 |
| 2022 | The correlation between genetic factors and freezing of gait in patients with Parkinson's disease | Radojević, Branislava; Dragašević-Mišković, Nataša ; Marjanović, Ana ; Branković, Marija ; Milovanović, Andona ; Petrović, Igor ; Svetel, Marina ; Jančić, Ivan ; Stanisavljević, Dejana ; Milićević, Ognjen ;
Savić, Miroslav
; Kostić, Vladimir ; | Article | 21M21 |
| 2021 | Phenotype characteristics of ANO10 mutation carries: a case series from Serbia and a systematic review of the literature | Stanković, 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 |
| 2021 | Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit | Miletić, Aleksandra; Ruml-Stojanović, Jelena ; Parezanović, Vojislav ; Rsovac, Snežana; Drakulić, Danijela ; Soldatović, Ivan ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Borlja, Nikola;
Milivojević, Milena
; Marjanović, Ana ; Branković, Marija ; Čuturilo, Goran ; | Article | 21aM21a |
| 2021 | Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot–Marie–Tooth disease type 1A | Bjelica, Bogdan ; Perić, Stojan ; Božović, Ivo ; Janković, Milena ; Branković, Marija ; Palibrk, Aleksa; Rakočević-Stojanović, Vidosava | Article | 22M22 |
| 2021 | Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review | Dawod, 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 |
| 2021 | Clinical 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 | Mp. category will be shown later |
| 2021 | Clinical 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 |
| 2021 | Selected genetic polymorphisms of COMT, DRD2, ANKK1, and DAT genes and the risk of psychosis in Parkinson's disease | Radojević, 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 |
| 2020 | Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy | Dawod, Phepy G. A.; Jančić, Jasna ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Samardžić, Janko ; Potkonjak, Dario ; Đurić, Vesna; Mesaroš, Šarlota ; Novaković, Ivana ;
Abdel Motaleb, Fayda I.; Kostić, Vladimir S.
; Nikolić, Dejan ; | Article | 21M21 |
| 2020 | Yield of the PMP22 deletion analysis in patients with compression neuropathies | Ivanović, Vukan ; Branković. Marija ; Bjelica, Bogdan ; Kačar, Aleksandra ; Tubić, Radoje ; Janković, Milena ; Marjanović, Ana ; Novaković, Ivana ; Rakočević-Stojanović, Vidosava ; Perić, Stojan | Article | 21M21 |
| 2020 | Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A | Bjelica, Bogdan ; Perić, Stojan Z. ; Božović, Ivo ; Basta, Ivana Z. ; Kačar, Aleksandra S. ; Janković, Milena Z. ; Branković, Marija ; Palibrk, Aleksa ; Novaković, Ivana V. ; Lavrnić, Dragana V. ;
Stević, Zorica D.
; Rakočević-Stojanović, Vidosava M. ; | Conference Paper | Mp. category will be shown later |
| 2020 | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies | Maksić, Jasmina ; Dobričić, Valerija ; Rasulić, Lukas ; Maksimović, Nela ; Branković, Marija ; Milić-Rašić, Vedrana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana | Article | 23M23 |