Researchers
Janković, Milena
Results 41-60 of 107
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | Clinical 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 | 21M21 |
| 2023 | Reply 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+ |
| 2023 | TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients | Pešić, Milica ; Andrejić, Nikola; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka | Conference Paper | Mp. category will be shown later |
| 2023 | The association of R47H variant in the TREM2 gene and genetic susceptibility to Alzheimer's disease in Serbian population | Andrejić, Nikola; Pešić, Milica ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka | Naučni članak | 53M53 - Nacionalni časopis kategorije M53 |
| 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
; | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 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 | 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. ; | Naučni članak | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
| 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 | The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options | Janković, Milena ; Petrović, Bojana ; Novaković, Ivana ; Branković, Slavko ; Radosavljević, Nataša ; Nikolić, Dejan | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 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 ; | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 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;
| Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2021 | Guillain-Barre Syndrome during pregnancy: case series | Arsenijević, Mirjana; Radišić, Vanja ; Janković, Milena Z. ; Perić, Stojan Z. ; Jovanović, Dejana R. ; Berisavac, Ivana I. | Conference Paper | Mp. category will be shown later |
| 2021 | Early predictors of mortality in patients with metabolic encephalopathy | Đurđević, 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 |
| 2021 | Novel TEAD1 gene variant in a Serbian family with Sveinsson's chorioretinal atrophy | Grubiša, Ivana ; Janković, Milena ; Nikolić, Nađa ; Jakšić, Vesna Z. ; Risimić, Dijana ; Mavija, Milka; Stamenković, Miroslav R. ; Zlatović, Mario ; Milašin, Jelena | Naučni članak | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
| 2021 | Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis | Janković, Milena ; Novaković, Ivana ; Gamil Anwar Dawod, Phepy; Gamil Anwar Dawod, Ayman; Drinić, Aleksandra; Abdel Motaleb, Fayda I.; Dučić, Sinisa ; Nikolić, Dejan | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2021 | Genetic and epigenomic modifiers of diabetic neuropathy | Janković, Milena ; Novaković, Ivana ; Nikolić, Dejan ; Mitrović-Maksić, Jasmina ; Branković, Slavko ; Petronić, Ivana ; Ćirović, Dragana ; Dučić, Siniša ; Grajić, Mirko ; Bogićević, Dragana | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 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 ; | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 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 | 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 | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2021 | The impact of ACA occlusion on the short-term functional outcome of patients treated with mechanical thrombectomy | Jankovic, 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 |