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V. Branković

Observed names: Brankovic, V., Branković, Vesna, V Brankovic, V. Brankovic, Vesna Brankovic, Vesna Branković, Vesna M. Brankovic
ORCID: 0000-0001-8582-1403
Observed ORCID: 0000-0001-8582-1403
OpenAlex ID: A5077608151
Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial
2021 · Eugenio Mercuri, Nicolas Deconinck, et al. · The Lancet Neurology · 255
Cardiac phenotype in ATP1A3 -related syndromes: A multicenter cohort study
2020 · Simona Balestrini, Mohamad A. Mikati, et al. · Neurology · 46
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Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders
2020 · Francesco Nicita, Monia Ginevrino, et al. · Journal of Medical Genetics · 46
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome
2020 · Claire Bar, Mathieu Kuchenbuch, et al. · Epilepsia · 44
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Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia
2016 · S. Barresi, M. Niceta, et al. · Clinical Genetics · 33
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia
2022 · Liedewei Van de Vondel, Jonathan De Winter, et al. · Movement Disorders · 28
Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3
2021 · Stefan A. Djordjevic, Vedrana Milic-Rasic, et al. · Neuromuscular Disorders · 28
A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine
2021 · Paola Imbrici, Elena Conte, et al. · International Journal of Molecular Sciences · 26
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Refining the mutational spectrum and gene–phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study
2021 · Sara Nuovo, Alessia Micalizzi, et al. · Journal of Medical Genetics · 21
GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia
2017 · Valerija Dobričić, Aleksandra Tomić, et al. · Parkinsonism & Related Disorders · 19
Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3
2020 · Stefan A. Djordjevic, Vedrana Milic‐Rasic, et al. · Muscle & Nerve · 17
ANO10 ‐Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series
2024 · Andona Milovanović, Ana Westenberger, et al. · Movement Disorders · 9
Novel unconventional variants expand the allelic spectrum of OPHN1 gene
2021 · Sara Nuovo, Vesna Brankovic, et al. · American Journal of Medical Genetics Part A · 9
Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3✰
2022 · S. Djordjevic, V. Milic-Rasic, et al. · Archives de Pédiatrie · 2
Phenotype of PLP1‐related Disorder Caused by Novel Mutation: A Case Report
2018 · Nikola Kresojević, Igor Petrović, et al. · Movement Disorders Clinical Practice · 2
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A novel in-frame deletion of OPHN1 in a family with syndromic X-linked mental retardation
2017 · V. Brankovic, S. Nuovo, et al. · European Journal of Paediatric Neurology
European pediatric normative values for the scale for assessment and rating of ataxia (SARA)
2016 · Lawerman, T. F., Brandsma, R., et al. · University of Groningen research database (University of Groningen / Centre for Information Technology)
European SARA age validation trial in children -Preliminary results-
2015 · Tjitske F Lawerman, Rick Brandsma, et al. · Movement Disorders
PP12.16 – 2973: Congenital cerebellar ataxias – Clinical, radiological and genetic considerations
2015 · V. Brankovic, A. Zekavica, et al. · European Journal of Paediatric Neurology
PP09.9 – 2907: Is it easy to recognize HINT1 neuropathy
2015 · V. Milic Rasic, V. Brankovic, et al. · European Journal of Paediatric Neurology
O4 – 2020 Electroneuromyography parameters in hereditary and congenital ataxia
2013 · V Milic Rasic, V Brankovic, et al. · European Journal of Paediatric Neurology
PP3.6 – 2106 Early onset ataxia – an international database
2013 · M Steinlin, P Baxter, et al. · European Journal of Paediatric Neurology
4.Electromyography test as diagnostic procedure in recessive cerebellar ataxias
2012 · V. Milic Rasic, S. Todorovic, et al. · Clinical Neurophysiology
P5.18 Electromyography findings in family with cerebellar ataxia and new genotype
2011 · V. Milic Rasic, S. Todorovic, et al. · Clinical Neurophysiology
P16.3 Neuromyotonia as a main sign of a possible new type of hereditary axonal neuropathy
2011 · V. Milić-Rašić, S. Todorovic, et al. · European Journal of Paediatric Neurology
Works count: 30
Citation count: 579
H-index: 11
I10-index: 11
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