еНаука - преглед
Преглед према Аутор Bergant, Gaber
Приказ резултата 1 до 7 од 7
| Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
|---|---|---|---|---|
| 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; | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 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 | 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 |
| 2018 | Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases | Bergant, Gaber; Maver, Ales; Lovrecic, Luca; Čuturilo, Goran ; Hodzic, Alenka; Peterlin, Borut | Article | 21a+M21a+ |
| 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 |
| 2026 | Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease | Bergant, Gaber; ...; Brankovic, Marija ; Jankovic, Milena Z ; Svetel, Marina ; ...; Dragasevic-Miskovic, Natasa; Petrovic, Igor; ...; Novakovic, Ivana ;
...; (broj, koautora 19);
| Article | 22M22 |
| 2019 | Results of clinical exome analysis in rare neurodegenerative disorders in Serbian population | Branković, Marija ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Svetel, Marina ; Petrović, Igor ; Perić, Stojan ; Janković, Milena ; Marjanović, Ana ; Stefanova, Elka ;
Novaković, Ivana
; Peterlin, Borut; Kostić, Vladimir ; | Conference Paper | Mp. category will be shown later |