@ARTICLE{
author={Ivanovic Vukan,Peric Stojan Z,Briggs Caitlin,Marjanovic Ana,Pesovic Jovan,Basta Ivana Z,Jansson Johan,Randhawa Simrat,Rajic Sonja,Gokhale Sankalp},
year={2026},
title={Hidden diagnoses among patients with double seronegative myasthenia gravis},
journal={FRONTIERS IN NEUROLOGY},
volume={17},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Ralic Branislav M,Albano Noemi,Viric Vanja,Nuredini Andi,Arsic-Azanjac Ana,Rajic Sonja,Marjanovic Ana,Tupler Rossella,Heatwole Chad,Peric Stojan Z},
year={2026},
title={Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy},
journal={FRONTIERS IN NEUROLOGY},
volume={17},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Milovanovic Andona,Jecmenica-Lukic Milica V,Mazalica Nina,Radisic Vanja,Djordjevic-Milosevic Maja,Marjanovic Ana,Brankovic Marija,Markovic Vladana V,Kresojevic Nikola D,Kostic Vladimir K,Dragasevic-Miskovic Natasa T},
year={2025},
title={Chorea in Hereditary Leukodystrophies - Overview of Two Cases},
journal={TREMOR AND OTHER HYPERKINETIC MOVEMENTS},
volume={15},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Vukojevic Milica,Marjanovic Ana,Ivanovic Vukan,Jankovic M,Kacar Aleksandra S,Basta Ivana Z,Peric S},
year={2025},
title={Hereditary neuropathies in Serbian population},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={32},
number={},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ralic Branislav M,Albano Noemi,Viric Vanja,Nuredini A,Azanjac Anja,Rajic Sonja,Marjanovic Ana,Tupler Rossella,Heatwole Chad,Peric Stojan Z},
year={2025},
title={Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy},
journal={NEUROMUSCULAR DISORDERS},
volume={53},
number={},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kresojevic Nikola D,Markovic Vladana V,Geratovic Cveta,Jecmenica-Lukic Milica V,Tomic Aleksandra D,Dobricic Valerija S,Stankovic Iva D,Stojkovic Tanja,Dragasevic Natasa T,Sarcevic Maksim,Jankovic Milena Z,Marjanovic Ana,Novakovic Ivana V,Kostic Vladimir K,Svetel Marina V,Petrovic Igor N},
year={2025},
title={Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?},
journal={NEUROLOGICAL SCIENCES},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Radojevic Branislava,Milovanovic Andona,Petrovic Igor N,Svetel Marina V,Marjanovic Ana,Jancic Ivan R,Stanisavljevic Dejana M,Milicevic Ognjen S,Savic Miroslav M,Kostic Vladimir S,Dragasevic-Miskovic Natasa T},
year={2025},
title={The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson's disease},
journal={NEUROLOGICAL RESEARCH},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Brankovic Marija,Han Heonjong,Jankovic Milena Z,Marjanovic Ana,Andrejic Nikola,Gunjic Ilija,Viric Vanja,Palibrk Aleksa,Lee Hane,Peric Stojan Z},
year={2024},
title={Secondary findings in 443 exome sequencing data},
journal={ANNALS OF HUMAN GENETICS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Stefanova Elka D,Marjanovic Ana,Dobricic Valerija S,Mandic-Stojmenovic Gorana B,Stojkovic Tanja,Brankovic Marija,Sarcevic Maksim,Novakovic Ivana V,Kostic Vladimir S},
year={2024},
title={Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center},
journal={NEUROGENETICS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Brankovic Marija,Ivanovic Vukan,Basta Ivana Z,...,Stevic Zorica D,Ralic Branislav M,Tubic Radoje M,...,Markovic Vladana V,Bozovic Ivo,Svetel Marina V,Marjanovic Ana,Veselinovic Nikola D,Mesaros Sarlota T,Jankovic Milena Z,Savic-Pavicevic Dusanka Lj,Jovin Zita B,Novakovic Ivana V,...,Peric Stojan Z},
year={2024},
title={Whole exome sequencing in Serbian patients with hereditary spastic paraplegia},
journal={NEUROGENETICS},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Milovanovic Andona,Dragasevic-Miskovic Natasa T,Thomsen Mirja,Borsche Max,Hinrichs Frauke,Westenberger Ana,Klein Christine,Brueggemann Norbert,Brankovic Marija,Marjanovic Ana,Svetel Marina V,Kostic Vladimir S,Lohmann Katja},
year={2024},
title={<i>RFC1 </i>and <i>FGF14</i> Repeat Expansions in Serbian Patients with Cerebellar Ataxia},
journal={MOVEMENT DISORDERS CLINICAL PRACTICE},
volume={11},
number={6},
pages={626-633},
document_type={Article},
} 

@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={Kresojevic Nikola D,Perovic Ivana,Stankovic Iva D,Tomic Aleksandra D,Jecmenica-Lukic Milica V,Markovic Vladana V,Stojkovic Tanja,Mandic Gorana B,Jankovic Milena Z,Marjanovic Ana,Brankovic Marija,Novakovic Ivana V,Petrovic Igor N,Dragasevic Natasa T,Stefanova Elka D,Svetel Marina V,Kostic Vladimir K},
year={2023},
title={Clinical and Genetic Features of Huntington's Disease Patients From Republic of Serbia: A Single-Center Experience},
journal={JOURNAL OF MOVEMENT DISORDERS},
volume={16},
number={3},
pages={333-335},
document_type={Letter},
} 

@ARTICLE{
author={Ivanovic Vukan,Brankovic Marija,Bozovic Ivo,Stevic Zorica D,Basta Ivana Z,Markovic Vladana V,Svetel Marina V,Tubic Radoje M,Marjanovic Ana,Veselinovic Nikola D,Mesaros Sarlota T,Jankovic Milena Z,Rakocevic-Stojanovic Vidosava M,Savic-Pavicevic Dusanka Lj,Novakovic Ivana V,Peric Stojan Z},
year={2023},
title={Whole exome sequencing in Serbian patients with hereditary spastic paraplegia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={30},
number={},
pages={260-260},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dragasevic-Miskovic Natasa T,Milovanovic Andona,Stankovic I,Marjanovic Ana,Brankovic Marija,Dobricic Valerija S,Petrovic Igor N,Svetel Marina V,Novakovic Ivana V,Kostic V},
year={2023},
title={Motor neuron involvement in facial muscles as characteristic of ANO10 mutation},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={30},
number={},
pages={234-234},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksic Jasmina,Maksimovic Nela S,Rasulic Lukas G,Milankov Olgica,Marjanovic Ana,Cvetkovic Dragana D,Rakocevic-Stojanovic Vidosava M,Novakovic Ivana V},
year={2023},
title={The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies},
journal={VOJNOSANITETSKI PREGLED},
volume={80},
number={3},
pages={201-207},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Markovic Vladana V,Dobricic Valerija S,Stankovic Iva D,Stojkovic Tanja,Tomic Aleksandra D,Jecmenica-Lukic Milica V,Jankovic Milena Z,Marjanovic Ana,Brankovic Marija,Novakovic Ivana V,Petrovic Igor N,Dragasevic Natasa T,Svetel Marina V,Kostic Vladimir K},
year={2023},
title={Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism"},
journal={MOVEMENT DISORDERS},
volume={38},
number={4},
pages={712-713},
document_type={Letter},
} 

@ARTICLE{
author={Marjanovic Ana,Palibrk Aleksa,Dobricic Valerija S,Milicevic Ognjen S,Brankovic Marija,Viric Vanja,Drinic Aleksandra,Mandic-Stojmenovic Gorana B,Jankovic Milena Z,Basta Ivana Z,Peric Stojan Z,Novakovic Ivana V,Stefanova Elka D,Stevic Zorica D},
year={2023},
title={C9orf72 Genetic Screening in Amyotrophic Lateral Sclerosis Patients from Serbia},
journal={GENETIKA-BELGRADE},
volume={55},
number={1},
pages={1-18},
document_type={Article},
} 

@ARTICLE{
author={Brankovic Marija,Stefanova Elka D,Mandic Gorana B,Marjanovic Ana,Dobricic Valerija S,Maver Ales,Bergant Gaber,Stevic Zorica D,Jankovic Milena Z,Novakovic Ivana V,Peterlin Borut,Kostic Vladimir K},
year={2022},
title={Analysis of "Clinical Exome" Panel in Serbian Patients with Cognitive Disorders},
journal={GENETIKA-BELGRADE},
volume={54},
number={3},
pages={1351-1364},
document_type={Article},
} 

@ARTICLE{
author={Marjanovic Ana,Dobricic Valerija S,Jecmenica-Lukic Milica V,Stankovic Iva D,Milicevic Ognjen S,Dragasevic-Miskovic Natasa T,Brankovic Marija,Jankovic Milena Z,Novakovic Ivana V,Svetel Marina V,Stefanova Elka D,Kostic Vladimir K},
year={2022},
title={C9ORF72 Repeat Expansion Is Not Associated with Atypical Parkinsonism in the Serbian Population},
journal={GENETIKA-BELGRADE},
volume={54},
number={3},
pages={1313-1330},
document_type={Article},
} 

@ARTICLE{
author={Brankovic Marija,Dragasevic Natasa T,Dobricic Valerija S,Maver Ales,Bergant Gaber,Petrovic Igor N,Peric Stojan Z,Marjanovic Ana,Jankovic Milena Z,Jancic Jasna B,Novakovic Ivana V,Peterlin Borut,Svetel Marina V,Kostic Vladimir K},
year={2022},
title={Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience},
journal={GENETIKA-BELGRADE},
volume={54},
number={1},
pages={395-409},
document_type={Article},
} 

@ARTICLE{
author={Radojevic Branislava,Dragasevic-Miskovic Natasa T,Marjanovic Ana,Brankovic Marija,Milovanovic Andona,Petrovic Igor N,Svetel Marina V,Jancic Ivan R,Stanisavljevic Dejana M,Milicevic Ognjen S,Savic Miroslav M,Kostic Vladimir S},
year={2022},
title={The correlation between genetic factors and freezing of gait in patients with Parkinson's disease},
journal={PARKINSONISM & RELATED DISORDERS},
volume={98},
number={},
pages={7-12},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Dobricic Valerija S,Jecmenica-Lukic Milica V,Tomic Aleksandra D,Petrovic Igor N,Dragasevic Natasa T,Perovic Ivana,Marjanovic Ana,Brankovic Marija,Jankovic Milena Z,Novakovic Ivana V,Svetel Marina V,Kostic Vladimir S},
year={2022},
title={Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience},
journal={JOURNAL OF NEUROLOGY},
volume={269},
number={6},
pages={3167-3174},
document_type={Article},
} 

@ARTICLE{
author={Dawod Phepy GA,Jancic Jasna B,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Samardzic Janko M,Dawod Ayman Gamil Anwar,Novakovic Ivana V,Abdel Motaleb Fayda I,Radlovic Vladimir N,Kostic Vladimir S,Nikolic Dejan P},
year={2021},
title={Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review},
journal={DIAGNOSTICS},
volume={11},
number={11},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Radojevic Branislava,Dragasevic-Miskovic Natasa T,Marjanovic Ana,Marjanovic Ana,Dobricic Valerija S,Milovanovic Andona,Tomic Aleksandra D,Svetel Marina V,Petrovic Igor N,Jancic Ivan R,Stanisavljevic Dejana M,Savic Miroslav M,Kostic Vladimir S},
year={2021},
title={Clinical and Genetic Analysis of Psychosis in Parkinson's Disease},
journal={JOURNAL OF PARKINSONS DISEASE},
volume={11},
number={4},
pages={1973-1980},
document_type={Article},
} 

@ARTICLE{
author={Miletic Aleksandra,Ruml-Stojanovic Jelena,Parezanovic Vojislav M,Rsovac Snezana,Drakulic Danijela D,Soldatovic Ivan A,Mijovic Marija,Bosankic Brankica,Petrovic Hristina,Borlja Nikola,Milivojevic Milena C,Marjanovic Ana,Marjanovic Ana,Cuturilo Goran},
year={2021},
title={Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit},
journal={EUROPEAN JOURNAL OF PEDIATRICS},
volume={180},
number={10},
pages={3219-3227},
document_type={Article},
} 

@ARTICLE{
author={Pesic Milica,Dragasevic-Miskovic Natasa T,Marjanovic Ana,Dobricic Valerija S,Maksimovic Nela S,Svetel Marina V,Perovic Dijana,Novakovic Ivana V,Cirkovic Sanja,Stankovic Iva D,Kostic Vladimir K},
year={2021},
title={Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism},
journal={NEUROLOGICAL RESEARCH},
volume={43},
number={4},
pages={321-326},
document_type={Article},
} 

@ARTICLE{
author={Pesic Milica,Maksimovic Nela S,Aleksic Andjelka,Gulic Milica,Djuranovic Ana S,Grk Milka B,Dusanovic-Pjevic Marija G,Stankovic Iva D,Markovic Vladana V,Marjanovic Ana,Novakovic Ivana V,Dragasevic-Miskovic Natasa T,Kostic Vladimir S},
year={2020},
title={Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={888-888},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dawod Phepy GA,Jancic Jasna B,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Samardzic Janko M,Potkonjak Dario,Djuric Vesna,Mesaros Sarlota T,Novakovic Ivana V,Abdel Motaleb Fayda I,Kostic Vladimir S,Nikolic Dejan P},
year={2020},
title={Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy},
journal={GENES},
volume={11},
number={9},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Radojevic Branislava,Dragasevic-Miskovic Natasa T,Marjanovic Ana,Milovanovic Andona,Svetel Marina V,Petrovic Igor N,Savic Miroslav M,Jancic Ivan R,Kostic Vladimir K},
year={2020},
title={The influence of ANNK1/DRD2 haplotypes on the onset of complications of long-term levodopa therapy in Parkinson's disease},
journal={MOVEMENT DISORDERS},
volume={35},
number={},
pages={S473-S474},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ivanovic Vukan,Marjanovic Ana,Bjelica Bogdan,Kacar Aleksandra S,Tubic Radoje M,Jankovic Milena Z,Marjanovic Ana,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z},
year={2020},
title={Yield of thePMP22deletion analysis in patients with compression neuropathies},
journal={JOURNAL OF NEUROLOGY},
volume={267},
number={12},
pages={3617-3623},
document_type={Article},
} 

@ARTICLE{
author={Bjelica Bogdan,Peric Stojan Z,Basta Ivana Z,Bozovic Ivo,Kacar Aleksandra S,Marjanovic Ana,Ivanovic Vukan,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2020},
title={Neuropathic pain in patients with Charcot-Marie-Tooth type 1A},
journal={NEUROLOGICAL SCIENCES},
volume={41},
number={3},
pages={625-630},
document_type={Article},
} 

@ARTICLE{
author={Ivancevic Nikola,Cerovac Natasa M,Nikolic Blazo,Cuturilo Goran,Marjanovic Ana,Marjanovic Ana,Novakovic Ivana V},
year={2019},
title={GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation},
journal={VOJNOSANITETSKI PREGLED},
volume={76},
number={5},
pages={543-546},
document_type={Article},
} 

@ARTICLE{
author={Dawod Phepy GA,Rovcanin Branislav R,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Motaleb Abdel F,Jancic Jasna B,Kostic Vladimir S},
year={2019},
title={Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={1836-1837},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Marjanovic Ana,Dobricic Valerija S,Brankovic Marija,Jankovic Milena Z,Mandic Gorana B,Stefanova Elka D,Stevic Zorica D,Novakovic Ivana V,Kostic Vladimir S},
year={2019},
title={Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={961-961},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Dobricic Valerija S,Marjanovic Ana,Brankovic Marija,Pavlovic Aleksandra M,Dujmovic Irena,Mijajlovic Milija D,Novakovic Ivana V,Kostic Vladimir S},
year={2019},
title={NOTCH3 mutations in Serbian CADASIL patients},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={293-293},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Brankovic M,Dobricic Valerija S,Svetel Marina V,Peric Stojan Z,Stefanova Elka D,Marjanovic Ana,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S},
year={2019},
title={Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: Firs experience},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={292-292},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dawod Phepy GA,Rovcanin Branislav R,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Dujmovic Irena,Jancic Jasna B,Kostic Vladimir S},
year={2019},
title={Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={181-181},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Andjus Stefan P,Nikolic Nadja S,Marjanovic Ana,Marjanovic Ana,Lazovic Vladimir M,Tubic Bojana P,Canak-Atlagic Jelena Z,Nikolic Vera P,Paunovic Momir M},
year={2019},
title={First record of freshwater sponge Trochospongilla horrida Weltner, 1893 in Serbia - A morphological and genetic study},
journal={LIMNOLOGICA},
volume={76},
number={},
pages={48-51},
document_type={Article},
} 

@ARTICLE{
author={Brankovic Marija,Kresojevic Nikola D,Marjanovic Ana,Novakovic Ivana V,Kostic Vladimir K},
year={2018},
title={NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={406-406},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Marjanovic Ana,Dobricic Valerija S,Marjanovic Ivan V,Brankovic Marija,Jankovic Milena Z,Mandic Gorana B,Stevic Zorica D,Novakovic Ivana V,Stefanova Elka D,Kostic Vladimir K},
year={2018},
title={C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={376-376},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Andjus Stefan P,Nikolic Nadja S,Dobricic Valerija S,Marjanovic Ana,Gacic Zoran M,Brankovic Goran O,Akovic Maja R,Paunovic Momir M},
year={2018},
title={Contribution to the knowledge on the distribution of freshwater sponges - the Danube and Sava rivers case study},
journal={JOURNAL OF LIMNOLOGY},
volume={77},
number={2},
pages={199-208},
document_type={Article},
} 

@ARTICLE{
author={Trifunovic Jovanka A,Basta-Jovanovic Gordana M,Nikolic Nadja S,Carkic Jelena,Marjanovic Ana,Marjanovic Ana,Radojevic-Skodric Sanja M,Prvanovic Mirjana,Jovanovic Aleksandar,Dzamic Zoran M,Milasin Jelena M},
year={2018},
title={HTERT promoter methylation and single nucleotide polymorphism (-245 T > C) affect renal cell carcinoma behavior in Serbian population},
journal={JOURNAL OF BUON},
volume={23},
number={6},
pages={1887-1892},
document_type={Article},
} 

@ARTICLE{
author={Peric Stojan Z,Heatwole Chad,Djurovic E,Kacar Aleksandra S,Nikolic Aleksandra L,Basta Ivana Z,Marjanovic Ana,Stevic Zorica D,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M},
year={2017},
title={Prospective measurement of quality of life in myotonic dystrophy type 1},
journal={ACTA NEUROLOGICA SCANDINAVICA},
volume={136},
number={6},
pages={694-697},
document_type={Article},
} 

@ARTICLE{
author={Peric Stojan Z,Vujnic Milorad,Dobricic Valerija S,Marjanovic Ana,Basta Ivana Z,Novakovic Ivana V,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M},
year={2016},
title={Five-year study of quality of life in myotonic dystrophy},
journal={ACTA NEUROLOGICA SCANDINAVICA},
volume={134},
number={5},
pages={346-351},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Marjanovic Ana,Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S},
year={2016},
title={HPCA-related dystonia: Too rare to be found?},
journal={MOVEMENT DISORDERS},
volume={31},
number={7},
pages={1071-1071},
document_type={Letter},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Zarkovic Milena,Tomic Aleksandra D,Marjanovic Ana,Westenberger Ana,Cvetkovic Dragana D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited},
journal={PARKINSONISM & RELATED DISORDERS},
volume={21},
number={10},
pages={1256-1259},
document_type={Article},
}