Autori: Brankovic Vesna
| Naslov | Developmental and epilepsy spectrum ofKCNB1encephalopathy with long-term outcome (Article) |
| Autori | Bar Claire ... Brankovic Vesna ... (broj koautora 61) |
| Info | EPILEPSIA, (2020), vol. 61 br. 11, str. 2461-2473 |
| Projekat | National Research Agency under the "Investissements d'avenir" programFrench National Research Agency (ANR) [ANR-10IAHU-01]; Bettencourt Schueller Foundation; French League Against Epilepsy; ERC Consolidator GrantEuropean Research Council (ERC); Curekids N |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia (Article) |
| Autori | Dobricic Valerija S Tomic Aleksandra D Brankovic Vesna Kresojevic Nikola D Jankovic Milena Z Westenberger Ana Milic-Rasic Vedrana M Klein Christine Novakovic Ivana V Svetel Marina V Kostic Vladimir S |
| Info | PARKINSONISM & RELATED DISORDERS, (2017), vol. 45 br. , str. 81-84 |
| Projekat | Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation; German Research Foundation (DFG) Research Unit [FOR2488] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia (Article) |
| Autori | Barresi S Niceta M Alfieri P Brankovic Vesna Piccini G Bruselles A Barone MR Cusmai Raffaella Tartaglia M Bertini E Zanni G |
| Info | CLINICAL GENETICS, (2017), vol. 91 br. 1, str. 86-91 |
| Projekat | Italian Telethon Foundation [GGP08145] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
