Autori: Brankovic Vesna
Naslov | Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3 (Article) |
Autori | Djordjevic Stefan A ![]() ![]() ![]() ![]() ![]() |
Info | MUSCLE & NERVE, (2021), vol. 63 br. 1, str. 75-83 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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Naslov | Cardiac phenotype in ATP1A3-related syndromes A multicenter cohort study (Article) |
Autori | Balestrini Simona ... Brankovic Vesna ... Potic Ana D ... (broj koautora 54) |
Info | NEUROLOGY, (2020), vol. 95 br. 21, str. E2866-E2879 |
Projekat | Epilepsy Society, UK; National Institute for Health Research Biomedical Research Centres funding scheme; Muir Maxwell Trust; National Institute of Neurological Disorders and Stroke [R01NS058949]; National Institute for Health Research Biomedical Centre at Great Ormond Street Hospital for Children NHS Foundation Trust; University College London; DFG-Grant [TR-128]; Duke Institute of Brain Sciences, Duke Research and discretionary funds; National Health and Medical Research Council of Australia; National Heart, Lung, and Blood Institute grant [F30 HL131217]; British Heart Foundation [RG/15/15/31742]; AHC UK; Max's Foundation (via the Great Ormond Street Hospital Children's Charity); MRC [MR/T024062/1] Funding Source: UKRI |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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Naslov | Cardiac Phenotype In ATP1A3 Related-Syndromes: A Multicentre Study (Meeting Abstract) |
Autori | Balestrini Simona ... Brankovic Vesna ... Potic Ana D ... (broj koautora 49) |
Info | EPILEPSIA, (2019), vol. 60 br. , Suppl. 2, str. 173-173 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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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 ![]() ![]() ![]() ![]() |
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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Treatment options in HINT1 neuropathy (Meeting Abstract) |
Autori | Nikodinovic-Glumac Jelena Milic-Rasic Vedrana M Brankovic Vesna Mladenovic Jelena M Todorovic Slobodanka |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2016), vol. 23 br. , Suppl. 2, str. 470-470 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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