@ARTICLE{
author={Milovanovic Andona,...,Stankovic Iva D,Tamas Olivera S,Brankovic Marija,Marjanovic Ana,...,Brankovic Vesna,Novakovic Ivana V,Petrovic Igor N,Svetel Marina V,...,Kostic Vladimir S,Dragasevic-Miskovic Natasa T},
year={2024},
title={<i>ANO10</i>-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series},
journal={MOVEMENT DISORDERS},
volume={39},
number={5},
pages={887-892},
document_type={Article},
} 

@ARTICLE{
author={Djordjevic Stefan A,Milic-Rasic Vedrana M,Brankovic Vesna,Kosac Ana P,Dejanovic-Djordjevic Ivana,Bijelic Maja,Dimkic-Tomic Tijana J,Markovic-Denic Ljiljana N,Kovacevic Smiljka,Petrovic Hristina,Vitorovic S,Dobric Z,Zdravkovic Vera M},
year={2022},
title={Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3},
journal={ARCHIVES DE PEDIATRIE},
volume={29},
number={7},
pages={480-483},
document_type={Article},
} 

@ARTICLE{
author={Van de Vondel Liedewei,...,Brankovic Vesna,...,(broj koautora 38)},
year={2022},
title={De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia},
journal={MOVEMENT DISORDERS},
volume={37},
number={6},
pages={1175-1186},
document_type={Article},
} 

@ARTICLE{
author={Nuovo Sara,...,Brankovic Vesna,...,(broj koautora 35)},
year={2022},
title={Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study},
journal={JOURNAL OF MEDICAL GENETICS},
volume={59},
number={4},
pages={399-409},
document_type={Article},
} 

@ARTICLE{
author={Imbrici Paola,Blunck Rikard,Conte Elena,Dinoi Giorgia,Liantonio Antonella,Brankovic Vesna,Zanni Ginevra},
year={2021},
title={A novel KCNA2 variant in a patient with cerebellar ataxia and epilepsy: functional characterization and sensitivity to 4-aminopyridine},
journal={EPILEPSIA},
volume={62},
number={},
pages={109-109},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Imbrici Paola,Conte Elena,Blunck Rikard,Stregapede Fabrizia,Liantonio Antonella,Tosi Michele,D'Adamo Maria Cristina,De Luca Annamaria,Brankovic Vesna,Zanni Ginevra},
year={2021},
title={A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={22},
number={18},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Nicita Francesco,...,Brankovic Vesna,...,(broj koautora 25)},
year={2021},
title={Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders},
journal={JOURNAL OF MEDICAL GENETICS},
volume={58},
number={7},
pages={475-483},
document_type={Article},
} 

@ARTICLE{
author={Zanni Ginevra,Blunck Rikard,Conte Elena,Brankovic Vesna,Liantonio Antonella,Imbrici Paola},
year={2021},
title={A novel de novo pathogenic variant in Kv1.2 potassium channel in a patient with cerebellar ataxia and epilepsy},
journal={EUROPEAN JOURNAL OF CLINICAL INVESTIGATION},
volume={51},
number={},
pages={158-158},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djordjevic Stefan A,Milic-Rasic Vedrana M,Brankovic Vesna,Kosac Ana P,Dejanovic-Djordjevic Ivana,Markovic-Denic Ljiljana N,Djuricic Goran J,Milcanovic Natasa,Kovacevic Smiljka,Petrovic Hristina,Djukic Milan M,Zdravkovic Vera M},
year={2021},
title={Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3},
journal={NEUROMUSCULAR DISORDERS},
volume={31},
number={4},
pages={291-299},
document_type={Article},
} 

@ARTICLE{
author={Nuovo Sara,Brankovic Vesna,Caputi Caterina,Casella Antonella,Nigro Vincenzo,Leuzzi Vincenzo,Valente Enza Maria},
year={2021},
title={Novel unconventional variants expand the allelic spectrum of OPHN1 gene},
journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A},
volume={185},
number={5},
pages={1575-1581},
document_type={Article},
} 

@ARTICLE{
author={Djordjevic Stefan A,Milic-Rasic Vedrana M,Brankovic Vesna,Kosac Ana P,Vukomanovic Goran V,Topalovic Mirko,Marinkovic Dejan,Mladenovic Jelena M,Pavlovic Andrija S,Bijelic Maja,Djukic Milan M,Markovic-Denic Ljiljana N},
year={2021},
title={Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3},
journal={MUSCLE & NERVE},
volume={63},
number={1},
pages={75-83},
document_type={Article},
} 

@ARTICLE{
author={Balestrini Simona,...,Brankovic Vesna,...,Potic Ana D,...,(broj koautora 54)},
year={2020},
title={Cardiac phenotype in ATP1A3-related syndromes A multicenter cohort study},
journal={NEUROLOGY},
volume={95},
number={21},
pages={E2866-E2879},
document_type={Article},
} 

@ARTICLE{
author={Bar Claire,...,Brankovic Vesna,...,(broj koautora 61)},
year={2020},
title={Developmental and epilepsy spectrum ofKCNB1encephalopathy with long-term outcome},
journal={EPILEPSIA},
volume={61},
number={11},
pages={2461-2473},
document_type={Article},
} 

@ARTICLE{
author={Balestrini Simona,...,Brankovic Vesna,...,Potic Ana D,...,(broj koautora 49)},
year={2019},
title={Cardiac Phenotype In ATP1A3 Related-Syndromes: A Multicentre Study},
journal={EPILEPSIA},
volume={60},
number={},
pages={173-173},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={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},
year={2017},
title={GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia},
journal={PARKINSONISM & RELATED DISORDERS},
volume={45},
number={},
pages={81-84},
document_type={Article},
} 

@ARTICLE{
author={Barresi S,Niceta M,Alfieri P,Brankovic Vesna,Piccini G,Bruselles A,Barone MR,Cusmai Raffaella,Tartaglia M,Bertini E,Zanni G},
year={2017},
title={Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia},
journal={CLINICAL GENETICS},
volume={91},
number={1},
pages={86-91},
document_type={Article},
} 

@ARTICLE{
author={Nikodinovic-Glumac Jelena,Milic-Rasic Vedrana M,Brankovic Vesna,Mladenovic Jelena M,Todorovic Slobodanka},
year={2016},
title={Treatment options in HINT1 neuropathy},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={23},
number={},
pages={470-470},
document_type={Meeting Abstract},
}