Researchers
Janković, Milena
Results 81-100 of 107
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Analysis 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 | Mp. category will be shown later |
| 2019 | Angiogenin 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 | Mp. category will be shown later |
| 2018 | Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease | Janković, Milena ; Dobričić, Valerija ; Kresojević, Nikola ; Marković, Vladana ; Petrović, Igor ; Svetel, Marina ; Pekmezović, Tatjana ; Novaković, Ivana ; Kostić, Vladimir | Article | 22M22 |
| 2018 | Unraveling ALS due to SOD1 mutation through the combination of brain and cervical cord MRI | Agosta, Federica; Spinelli, Edoardo Gioele; Marjanović, Ivan V.; Stević, Zorica ; Pagani, Elisabetta; Valsasina, Paola; Salak-Đokić, Biljana; Janković, Milena ; Lavrnić, Dragana ; Kostić, Vladimir ;
Filippi, Massimo;
| Article | 21a+M21a+ |
| 2018 | Features 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 | Mp. category will be shown later |
| 2018 | Analysis 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 | Mp. category will be shown later |
| 2018 | Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease | Janković, Milena Z. ; Dobričić, Valerija S. ; Kresojević, Nikola D. ; Marković, Vladana V. ; Petrović, Igor N. ; Svetel, Marina V. ; Pekmezović, Tatjana D. ; Novaković, Ivana V. ; Kostić, Vladimir K. | Conference Paper | Mp. category will be shown later |
| 2018 | C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders | Marjanović, Ana ; Dobričić, Valerija S. ; Marjanović, Ivan V. ; Branković, Marija ; Janković, Milena Z ; Mandić, Gorana B. ; Stević, Zorica D. ; Novaković, Ivana V. ; Stefanova, Elka D. ; Kostić, Vladimir K. | Conference Paper | Mp. category will be shown later |
| 2017 | Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia | Marjanović, Ivan V.; Selak-Đokić, Biljana; Perić, Stojan Z. ; Janković, Milena Z. ; Arsenijević, Vladimir; Basta, Ivana Z. ; Lavrnić, Dragana V. ; Stefanova, Elka D. ; Stević, Zorica D. | Article | 21M21 |
| 2017 | Study of ATXN2 repeath length in C9ORF72 expansion carriers | Marjanović, Ana ; Dobričić, Valerija ; Marjanović, Ivan ; Branković, Marija ; Janković, Milena ; Mandić, Gordana; Stefanova, Elka ; Stević, Zorica ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2017 | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia | Dobričić, Valerija ; Tomić, Aleksandra ; Branković, Vesna; Kresojević, Nikola ; Janković, Milena ; Westenberger, Ana; Milić Rašić, Vedrana ; Klein, Christine; Novaković, Ivana ; Svetel, Marina ;
Kostić, Vladimir
; | Article | 21aM21a |
| 2017 | PANK2 gene mutation spectrum in Serbian patients with neurodegeneration with brain iron accumulation | Novaković, Ivana ; Svetel, Marina ; Hartig, Monika; Dobričić, Valerija ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Krajnović, Maja; Cvetković, Dragana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2017 | First report of angiogenin gene mutations in patients with amyotrophic lateral sclerosis in Serbia | Janković, Milena ; Marjanović, Ivan ; Marjanović, Ana ; Perić, Stojan ; Basta, Ivana ; Novaković, Ivana ; Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2017 | Next generation sequencing in dystonia - our experience | Novaković, Ivana ; Branković, Marija ; Marjanovic, Ana ; Janković, Milena ; Dobričić, Valerija ; Stojiljković, Maja ; Petrović, Igor ; Pavlović, Sonja ; Svetel, Marina ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2017 | SOD1, TDP-43, FUS/TLS and C9orf72 genes in Serbian ALS patients: long term survey | Keckarević, Dušan P. ; Janković, Milena ; Gagić, Milica; Keckarević-Marković, Milica P. ; Kecmanović, Miljana M. ; Marjanović, Ana S. ; Marjanović, Ivan V. ; Novaković, Ivana V. ; Stević, Zorica D. | Conference Paper | Mp. category will be shown later |
| 2017 | Analysis 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 | Mp. category will be shown later |
| 2016 | Genetic mutations in Frontemporal dementia - report from the memory clinic from Serbia | Stefanova, Elka D. ; Mandić, Gorana B. ; Dobričić, Valerija S. ; Stojković, Tanja ; Janković, Milena Z. ; Novaković, Ivana V. ; Kostić, Vladimir S. | Conference Paper | Mp. category will be shown later |
| 2015 | Presenting symptoms of GBA-related Parkinson's disease | Kresojević, Nikola D. ; Janković, Milena Z. ; Petrović, Igor N. ; Kumar, Kishore R.; Dragašević, Nataša T. ; Dobričić, Valerija S. ; Novaković, Ivana V. ; Svetel, Marina V. ; Klein, Christine; Pekmezović, Tatjana D. ;
Kostić, Vladimir K.
; | Conference Paper | Mp. category will be shown later |
| 2015 | Identification of novel mutations in LRRK2 gene in patients with Parkinson's disease | Janković, Milena Z. ; Kresojević, Nikola D. ; Dobričić, Valerija S. ; Marković, Vladana V. ; Petrović, Igor N. ; Novaković, Ivana V. ; Kostić, Vladimir S. | Conference Paper | Mp. category will be shown later |
| 2015 | Are Lebers mitochondial DNA mutations associated with aquaporin-4 autoimmunity? | Dujmović, Irena ; Jančić, Jasna ; Dobričić, Valerija ; Janković, Milena ; Novaković, Ivana ; Comabella, Manuel; Drulović, Jelena | Contribution to periodical | 21aM21a |