@ARTICLE{
author={Kovacevic Gordana S,Todorovic Slobodanka,Novakovic Ivana V,Dobricic Valerija S,Savic-Pavicevic Dusanka Lj,Milic-Rasic Vedrana M,Svetel Marina V,Brkusanin Milos,Vukomanovic Vladislav A,Vucinic Dragana M,Ostojic Slavica B,Putnik Jovana,Kosac Ana P},
year={2025},
title={Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia},
journal={BIOMEDICINES},
volume={13},
number={11},
pages={-},
document_type={Article},
} 

@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={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={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={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={Foddis Marco,...,Pavlovic Aleksandra M,Kostic Vladimir S,Dobricic Valerija S,...,(broj koautora 29)},
year={2023},
title={TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients},
journal={NEUROBIOLOGY OF AGING},
volume={123},
number={},
pages={208-215},
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={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={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={Radojevic B,Dragasevic Natasa T,Milovanovic A,Brankovic Marija,Svetel Marina V,Dobricic Valerija S,Petrovic Igor N,Savic M,Stanisavljevic Dejana M,Kostic Vladimir K},
year={2021},
title={Selected genetic polymorphisms of COMT, DRD2, ANKK1, and DAT genes and the risk of psychosis in Parkinson's disease},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={28},
number={},
pages={352-352},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Messerschmidt Clemens,...,Pavlovic Aleksandra M,Kostic Vladimir K,Dobricic Valerija S,...,(broj koautora 34)},
year={2021},
title={PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice},
journal={SCIENTIFIC REPORTS},
volume={11},
number={1},
pages={-},
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={Maksic Jasmina,Dobricic Valerija S,Rasulic Lukas G,Maksimovic Nela S,Brankovic Marija,Milic-Rasic Vedrana M,Rakocevic-Stojanovic Vidosava M,Novakovic Ivana V},
year={2020},
title={Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies},
journal={VOJNOSANITETSKI PREGLED},
volume={77},
number={4},
pages={387-394},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Mandic-Stojmenovic Gorana B,Dobricic Valerija S,Petrovic Igor N,Brajkovic Leposava D,Stefanova Elka D,Svetel Marina V,Kostic Vladimir K},
year={2020},
title={Very Late-Onset Niemann Pick Type C Disease: Example of Progressive Supranuclear Palsy Look-Alike Disorder},
journal={MOVEMENT DISORDERS CLINICAL PRACTICE},
volume={7},
number={2},
pages={211-214},
document_type={Editorial Material},
} 

@ARTICLE{
author={Ebrahimi Keramatollah,Sabljak Predrag V,Simic Aleksandar P,Skrobic Ognjan M,Velickovic Dejan,Sljukic Vladimir M,Novakovic Ivana V,Dobricic Valerija S,Micev Marjan T,Pasko Predrag},
year={2019},
title={Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients},
journal={VOJNOSANITETSKI PREGLED},
volume={76},
number={12},
pages={1268-1273},
document_type={Article},
} 

@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={Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 33)},
year={2019},
title={Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={252-253},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mandic-Stojmenovic Gorana B,Stefanova Elka D,Novakovic Ivana V,Dobricic Valerija S,Stojkovic Tanja,Kostic Vladimir K},
year={2019},
title={The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={26},
number={},
pages={120-120},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Dobricic Valerija S,Kresojevic Nikola D,Markovic Vladana V,Petrovic Igor N,Svetel Marina V,Pekmezovic Tatjana D,Novakovic Ivana V,Kostic Vladimir K},
year={2018},
title={Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={410-411},
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={Jankovic Milena Z,Dobricic Valerija S,Kresojevic Nikola D,Markovic Vladana V,Petrovic Igor N,Svetel Marina V,Pekmezovic Tatjana D,Novakovic Ivana V,Kostic Vladimir K},
year={2018},
title={Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={393},
number={},
pages={27-30},
document_type={Article},
} 

@ARTICLE{
author={Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 30)},
year={2018},
title={Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients},
journal={PUBLIC HEALTH GENOMICS},
volume={21},
number={},
pages={17-17},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kulikovskaja Leonora,Sarajlija Adrijan,Savic-Pavicevic Dusanka Lj,Dobricic Valerija S,Klein Christine,Westenberger Ana},
year={2018},
title={WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype},
journal={NEUROLOGY-GENETICS},
volume={4},
number={2},
pages={-},
document_type={Editorial Material},
} 

@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={Mitropoulos Konstantinos,...,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S,...,(broj koautora 33)},
year={2017},
title={Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients},
journal={HUMAN GENOMICS},
volume={11},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Lohmann Katja,...,Dobricic Valerija S,...,Savic-Pavicevic Dusanka Lj,...,(broj koautora 18)},
year={2017},
title={Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans},
journal={HUMAN MOLECULAR GENETICS},
volume={26},
number={6},
pages={1078-1086},
document_type={Article},
} 

@ARTICLE{
author={Maric Nadja P,Mihaljevic Marina M,Franic Dusanka,Soldatovic Ivan A,Andric Sanja V,Lukic Iva S,Mirjanic Tijana,Stankovic Biljana B,Zukic Branka,Dobricic Valerija S,Novakovic Ivana V,Pavlovic Sonja T,Adzic Miroslav},
year={2017},
title={The Signature of Trauma in Psychosis: a Preliminary Genetic and Epigenetic Analyses of FK506-Binding Protein 5 Regulation},
journal={SCHIZOPHRENIA BULLETIN},
volume={43},
number={},
pages={S66-S66},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kostic Milutin V,Munjiza Ana M,Pesic Danilo R,Peljto Amir N,Novakovic Ivana V,Dobricic Valerija S,Lecic-Tosevski Dusica M,Mijajlovic Milija D},
year={2017},
title={A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder},
journal={JOURNAL OF AFFECTIVE DISORDERS},
volume={209},
number={},
pages={66-70},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Tomic Aleksandra D,Mijajlovic Milija D,Dobricic Valerija S,Novakovic Ivana V,Pekmezovic Tatjana D,Brajkovic Lela,Kostic Vladimir S},
year={2017},
title={Transcranial sonography in dopa-responsive dystonia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={24},
number={1},
pages={161-166},
document_type={Article},
} 

@ARTICLE{
author={Tomic Aleksandra D,Petrovic Igor N,Svetel Marina V,Dobricic Valerija S,Dragasevic-Miskovic Natasa T,Kostic Vladimir K},
year={2016},
title={Prospective study of disease progression in atypical form of pantothenate-kinase-associated neurodegeneration (PKAN)},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={23},
number={},
pages={811-811},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peric Stojan Z,Mandic-Stojmenovic Gorana B,Ilic Vera,Kovacevic Masa,Parojcic Aleksandra,Dobricic Valerija S,Pesovic Jovan,Novakovic Ivana V,Savic-Pavicevic Dusanka Lj,Rakocevic-Stojanovic Vidosava M},
year={2016},
title={Clusters of cognitive impairment among different forms of myotonic dystrophies},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={23},
number={},
pages={550-550},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dragasevic-Miskovic Natasa T,Domingo Aloysius,Dobricic Valerija S,Max Christoph,Braenne Ingrid,Petrovic Igor N,Grutz Karen,Pawlack Heike,Tournev Ivailo,Kalaydjieva Luba,Svetel Marina V,Lohmann Katja,Kostic Vladimir S,Westenberger Ana},
year={2016},
title={Seemingly Dominant Inheritance of a Recessive ANO10 Mutation in Romani Families With Cerebellar Ataxia},
journal={MOVEMENT DISORDERS},
volume={31},
number={12},
pages={1929-1931},
document_type={Letter},
} 

@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={Stefanova Elka D,Mandic Gorana B,Dobricic Valerija S,Stojkovic Tanja,Jankovic Milena Z,Novakovic Ivana V,Kostic Vladimir S},
year={2016},
title={Genetic mutations in Frontemporal dementia - report from the memory clinic from Serbia},
journal={JOURNAL OF NEUROCHEMISTRY},
volume={138},
number={},
pages={326-326},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kostic Milutin V,Canu Elisa,Agosta Federica,Munjiza Ana M,Novakovic Ivana V,Dobricic Valerija S,Ferraro Pilar Maria,Miler-Jerkovic Vera M,Pekmezovic Tatjana D,Lecic-Tosevski Dusica M,Filippi Massimo},
year={2016},
title={The Cumulative Effect of Genetic Polymorphisms on Depression and Brain Structural Integrity},
journal={HUMAN BRAIN MAPPING},
volume={37},
number={6},
pages={2173-2184},
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={Vuletic Vladimira,Chudy Darko,Almahariq Fadi,Dobricic Valerija S,Kostic Vladimir K,Bogdanovic Nenad},
year={2016},
title={Excellent outcome of pallidal deep brain stimulation in DYT6 dystonia: A case report},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={366},
number={},
pages={18-19},
document_type={Letter},
} 

@ARTICLE{
author={Radovanovic Sasa M,Peric Stojan Z,Savic-Pavicevic Dusanka Lj,Dobricic Valerija S,Pesovic Jovan,Kostic Vladimir K,Rakocevic-Stojanovic Vidosava M},
year={2016},
title={Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking},
journal={GAIT & POSTURE},
volume={44},
number={},
pages={194-199},
document_type={Article},
} 

@ARTICLE{
author={Dujmovic Irena,Jancic Jasna B,Dobricic Valerija S,Jankovic Slavko M,Novakovic Ivana V,Comabella Manuel,Drulovic Jelena S},
year={2016},
title={Are Leber's mitochondial DNA mutations associated with aquaporin-4 autoimmunity?},
journal={MULTIPLE SCLEROSIS JOURNAL},
volume={22},
number={3},
pages={393-394},
document_type={Letter},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Cuturilo Goran,Maksimovic Nela S,Dimitrijevic Nikola,Mitic Vesna,Jekic Biljana B,Lukovic Ljiljana F,Bunjevacki Vera I,Varljen Tatjana J,Dobricic Valerija S,Jovanovic Ida V,Kostic Vladimir S,Novakovic Ivana V},
year={2015},
title={Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities},
journal={TURKISH JOURNAL OF PEDIATRICS},
volume={57},
number={2},
pages={154-160},
document_type={Article},
} 

@ARTICLE{
author={Kostic Milutin V,Canu Elisa,Munjiza Ana M,Agosta Federica,Novakovic Ivana V,Dobricic Valerija S,Jerkovic Vera M,Miler-Jerkovic Vera M,Pekmezovic Tatjana D,Lecic-Tosevski Dusica M,Filippi Massimo},
year={2015},
title={Effect of accumulation of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms on brain morphology in patients with major depressive disorder},
journal={EUROPEAN NEUROPSYCHOPHARMACOLOGY},
volume={25},
number={},
pages={S395-S395},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Canu Elisa,Kostic Milutin V,Munjiza Ana M,Agosta Federica,Novakovic Ivana V,Dobricic Valerija S,Miler-Jerkovic Vera M,Pekmezovic Tatjana D,Lecic-Tosevski Dusica M,Filippi Massimo},
year={2015},
title={Three-way interaction of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms and its effect on regional gray matter volume in patients with major depressive disorder},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={629-629},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mandic-Stojmenovic Gorana B,Stefanova Elka D,Dobricic Valerija S,Novakovic Ivana V,Stojkovic Tanja,Jesic Aleksandar Z,Kostic Vladimir S},
year={2015},
title={Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia},
journal={DEMENTIA AND GERIATRIC COGNITIVE DISORDERS},
volume={40},
number={5-6},
pages={358-365},
document_type={Article},
} 

@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},
} 

@ARTICLE{
author={Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Basta Ivana Z,Dobricic Valerija S,Ralic Vesna,Kacar Aleksandra S,Peric Marina,Novakovic Ivana V},
year={2015},
title={Variability of multisystemic features in myotonic dystrophy type 1-lessons from Serbian registry},
journal={NEUROLOGICAL RESEARCH},
volume={37},
number={11},
pages={939-944},
document_type={Article},
} 

@ARTICLE{
author={Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Ralic Vesna,Milicevic Mihailo,Dobricic Valerija S},
year={2015},
title={Shorter CTG repeats length in an oligodendroglioma from a myotonic dystrophy type 1 patient},
journal={ACTA NEUROLOGICA BELGICA},
volume={115},
number={3},
pages={505-507},
document_type={Letter},
} 

@ARTICLE{
author={Vujnic Milorad,Peric Stojan Z,Popovic Srdjan S,Raseta Nela,Ralic Vesna,Dobricic Valerija S,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2015},
title={Metabolic syndrome in patients with myotonic dystrophy type 1},
journal={MUSCLE & NERVE},
volume={52},
number={2},
pages={273-277},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Jankovic Milena Z,Petrovic Igor N,Kumar Kishore R,Dragasevic Natasa T,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Klein Christine,Pekmezovic Tatjana D,Kostic Vladimir S},
year={2015},
title={Presenting symptoms of GBA-related Parkinson's disease},
journal={PARKINSONISM & RELATED DISORDERS},
volume={21},
number={7},
pages={804-807},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Jankovic Milena Z,Petrovic Igor N,Kumar Kishore R,Dragasevic Natasa T,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Klein Christine,Pekmezovic Tatjana D,Kostic Vladimir K},
year={2015},
title={Presenting symptoms of GBA-related Parkinson's disease},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={437-437},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Svetel Marina V,Tomic Aleksandra D,Dobricic Valerija S,Novakovic Ivana V,Dragasevic-Miskovic Natasa T,Petrovic Igor N,Kostic Vladimir K},
year={2015},
title={Dopa-responsive dystonia in the Serbian population: clinical and genetical characteristics},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={393-393},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Kresojevic Nikola D,Dobricic Valerija S,Markovic Vladana V,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={Identification of novel mutations in LRRK2 gene in patients with Parkinson's disease},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={354-354},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Zarkovic Milena,Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={A novel TOR1A mutation in a Serbian patient with cervical dystonia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={260-260},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peric Stojan Z,Paunic Teodora,Dobricic Valerija S,Novakovic Ivana V,Basta Ivana Z,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M},
year={2015},
title={Echocardiography in patients with myotonic dystrophy type 1},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={205-205},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic Milena Z,Kresojevic Nikola D,Dobricic Valerija S,Markovic Vladana V,Petrovic Igor N,Novakovic Ivana V,Kostic Vladimir S},
year={2015},
title={Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={353},
number={1-2},
pages={59-62},
document_type={Article},
} 

@ARTICLE{
author={Tomic Aleksandra D,Petrovic Igor N,Svetel Marina V,Dobricic Valerija S,Dragasevic-Miskovic Natasa T,Kostic Vladimir S},
year={2015},
title={Pattern of disease progression in atypical form of pantothenate-kinase-associated neurodegeneration (PKAN) - Prospective study},
journal={PARKINSONISM & RELATED DISORDERS},
volume={21},
number={5},
pages={521-524},
document_type={Article},
} 

@ARTICLE{
author={Peric Stojan Z,Mandic-Stojmenovic Gorana B,Stefanova Elka D,Savic-Pavicevic Dusanka Lj,Pesovic Jovan,Ilic Vera,Dobricic Valerija S,Basta Ivana Z,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M},
year={2015},
title={Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2},
journal={JOURNAL OF NEUROLOGY},
volume={262},
number={1},
pages={142-148},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Dragasevic Natasa T,Petrovic Igor N,Kostic Vladimir S},
year={2014},
title={Clinical and genetic characteristics of dopa-responsive dystonia in Serbian population},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={},
pages={S433-S433},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vujnic Milorad,Peric Stojan Z,Dobricic Valerija S,Ralic Vesna,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2014},
title={Metabolic syndrome in patients with myotonic dystrophy type 1},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={},
pages={S347-S347},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ziegan Julia,Wittstock Matthias,Westenberger Ana,Dobricic Valerija S,Wolters Alexander,Benecke Reiner,Klein Christine,Kamm Christoph},
year={2014},
title={Novel GNAL Mutations in Two German Patients With Sporadic Dystonia},
journal={MOVEMENT DISORDERS},
volume={29},
number={14},
pages={1833-1834},
document_type={Letter},
} 

@ARTICLE{
author={Kresojevic Nikola D,Dobricic Valerija S,Svetel Marina V,Kostic Vladimir S},
year={2014},
title={Mutations in Niemann Pick type C gene are risk factor for Alzheimer's disease},
journal={MEDICAL HYPOTHESES},
volume={83},
number={5},
pages={559-562},
document_type={Article},
} 

@ARTICLE{
author={Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Madzarevic R,Dobricic Valerija S,Ralic Vesna,Ilic Vera,Basta Ivana Z,Nikolic Aleksandra L,Stefanova Elka D},
year={2014},
title={Significant impact of behavioral and cognitive impairment on quality of life in patients with myotonic dystrophy type 1},
journal={CLINICAL NEUROLOGY AND NEUROSURGERY},
volume={126},
number={},
pages={76-81},
document_type={Article},
} 

@ARTICLE{
author={Kostic Vladimir S,Dobricic Valerija S,Stankovic Iva D,Ralic Vesna,Stefanova Elka D},
year={2014},
title={C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={10},
pages={1917-1921},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Westenberger Ana,Svetel Marina V,Tomic Aleksandra D,Ralic Vesna,Petrovic Igor N,Jecmenica-Lukic Milica V,Lohmann Katja,Novakovic Ivana V,Klein Christine,Kostic Vladimir S},
year={2014},
title={De Novo Mutation in the GNAL Gene Causing Seemingly Sporadic Dystonia in a Serbian Patient},
journal={MOVEMENT DISORDERS},
volume={29},
number={9},
pages={1190-1193},
document_type={Article},
} 

@ARTICLE{
author={Peric Stojan Z,Pavlovic Aleksandra M,Ralic Vesna,Dobricic Valerija S,Basta Ivana Z,Lavrnic Dragana V,Rakocevic-Stojanovic Vidosava M},
year={2014},
title={Transcranial Sonography in Patients with Myotonic Dystrophy Type 1},
journal={MUSCLE & NERVE},
volume={50},
number={2},
pages={278-282},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Dragasevic Natasa T,Petrovic Igor N,Kostic Vladimir S},
year={2014},
title={Clinical and genetic characteristics of dopa-responsive dystonia in a Serbian population},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={21},
number={},
pages={668-668},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vujnic Milorad,Peric Stojan Z,Dobricic Valerija S,Ralic Vesna,Novakovic Ivana V,Rakocevic-Stojanovic Vidosava M},
year={2014},
title={Metabolic syndrome in patients with myotonic dystrophy type 1},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={21},
number={},
pages={528-528},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Svetel Marina V,Pekmezovic Tatjana D,Markovic Vladana V,Novakovic Ivana V,Dobricic Valerija S,Djuric Gordana M,Stefanova Elka D,Kostic Vladimir S},
year={2013},
title={No Association between Brain-Derived Neurotrophic Factor G196A Polymorphism and Clinical Features of Parkinson's Disease},
journal={EUROPEAN NEUROLOGY},
volume={70},
number={5-6},
pages={257-262},
document_type={Article},
} 

@ARTICLE{
author={Mijajlovic Milija D,Kresojevic Nikola D,Peric Stojan Z,Pavlovic Aleksandra M,Svetel Marina V,Jankovic Milena Z,Dobricic Valerija S,Novakovic Ivana V,Lakocevic Milan B,Kostic Vladimir S},
year={2013},
title={Transcranial brain parenchyma sonography in Parkinson's disease with glucocerebrosidase mutations},
journal={CEREBROVASCULAR DISEASES},
volume={35},
number={},
pages={59-59},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keller Annika,...,Dobricic Valerija S,...,(broj koautora 49)},
year={2013},
title={Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice},
journal={NATURE GENETICS},
volume={45},
number={9},
pages={1077-+},
document_type={Article},
} 

@ARTICLE{
author={Pavlovic Aleksandra M,Dobricic Valerija S,Semnic Robert R,Lackovic Vesna B,Novakovic Ivana V,Bajcetic Milos I,Sternic Nadezda M},
year={2013},
title={A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family},
journal={ACTA NEUROLOGICA BELGICA},
volume={113},
number={3},
pages={299-302},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Djuric Gordana M,Novakovic Ivana V,Dobricic Valerija S,Stefanova Elka D,Kresojevic Nikola D,Tomic Aleksandra D,Jankovic Milena Z,Petrovic Igor N,Pekmezovic Tatjana D,Kostic Vladimir S},
year={2013},
title={A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia},
journal={ACTA NEUROLOGICA BELGICA},
volume={113},
number={3},
pages={243-245},
document_type={Article},
} 

@ARTICLE{
author={Tomic Aleksandra D,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Pekmezovic Tatjana D,Kresojevic Nikola D,Potrebic Aleksandra,Kostic Vladimir S},
year={2013},
title={Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia},
journal={VOJNOSANITETSKI PREGLED},
volume={70},
number={5},
pages={457-462},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Mijajlovic Milija D,Peric Stojan Z,Pavlovic Aleksandra M,Svetel Marina V,Jankovic Milena Z,Dobricic Valerija S,Novakovic Ivana V,Lakocevic Milan B,Klein Christine,Kostic Vladimir S},
year={2013},
title={Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations},
journal={PARKINSONISM & RELATED DISORDERS},
volume={19},
number={4},
pages={431-435},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Svetel Marina V,Jankovic Milena Z,Petrovic Igor N,Tomic Aleksandra D,Novakovic Ivana V,Kostic Vladimir S},
year={2013},
title={Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia},
journal={JOURNAL OF NEUROLOGY},
volume={260},
number={4},
pages={1037-1042},
document_type={Article},
} 

@ARTICLE{
author={Hsu Sandy Chan,...,Dobricic Valerija S,...,Jankovic Milena Z,...,Kostic Vladimir S,...,Novakovic Ivana V,...,(broj koautora 52)},
year={2013},
title={Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification},
journal={NEUROGENETICS},
volume={14},
number={1},
pages={11-22},
document_type={Article},
} 

@ARTICLE{
author={Kontic Milica Dj,Stojsic Jelena M,Stevic Ruza S,Bunjevacki Vera I,Jekic Biljana B,Dobricic Valerija S},
year={2013},
title={Could Spindle Cell Lung Carcinoma be Considered and Treated as Sarcoma, According to its Clinical Course, Morphology, Immunophenotype and Genetic Finding?},
journal={PATHOLOGY & ONCOLOGY RESEARCH},
volume={19},
number={1},
pages={129-133},
document_type={Article},
} 

@ARTICLE{
author={Dobricic Valerija S,Stefanova Elka D,Jankovic Milena Z,Gurunlian Nicole,Novakovic Ivana V,Hardy John,Kostic Vladimir S,Guerreiro Rita},
year={2012},
title={Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort},
journal={NEUROBIOLOGY OF AGING},
volume={33},
number={7},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Mitic Vesna,Cuturilo Goran,Novakovic Ivana V,Dimitrijevic Nikola,Damnjanovic Tatjana M,Dimitrijevic Aleksandar N,Dobricic Valerija S,Kostic Vladimir S,Radlovic Nedeljko P},
year={2011},
title={Epilepsy in a Child with Wolf-Hirschhorn Syndrome},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={139},
number={11-12},
pages={795-799},
document_type={Article},
} 

@ARTICLE{
author={Tomic Aleksandra D,Svetel Marina V,Novakovic Ivana V,Dobricic Valerija S,Kresojevic Nikola D,Kostic Vladimir S},
year={2011},
title={Mutational Analysis of ATP7B Gene and Genotype-Phenotype Correlation in Patients with Wilson's Disease From Serbia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={18},
number={},
pages={488-488},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kostic Vladimir S,Jecmenica-Lukic Milica V,Novakovic Ivana V,Dobricic Valerija S,Brajkovic Lela,Krajinovic Maja,Klein Christine,Pavlovic Aleksandra M},
year={2011},
title={Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification},
journal={JOURNAL OF NEUROLOGY},
volume={258},
number={9},
pages={1637-1642},
document_type={Article},
} 

@ARTICLE{
author={Jekic Biljana B,Bunjevacki Vera I,Dobricic Valerija S,Novakovic Ivana V,Milasin Jelena M,Popovic Branka M,Damnjanovic Tatjana M,Maksimovic Nela S,Perovic Vladimir R,Lukovic Ljiljana F},
year={2011},
title={Npm1 Gene Mutations in Children with Myelodysplastic Syndromes},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={63},
number={3},
pages={649-653},
document_type={Article},
} 

@ARTICLE{
author={Ivkovic Maja,Zamurovic Ljubica,Jovanovic Aleksandar A,Dobricic Valerija S,Damjanovic Aleksandar G,Savic-Pavicevic Dusanka Lj,Romac Stanka P},
year={2011},
title={Retinoic acid induced 1 gene and clinical subtypes of schizophrenia: An association study},
journal={PSYCHIATRY RESEARCH},
volume={188},
number={2},
pages={297-298},
document_type={Letter},
} 

@ARTICLE{
author={Kresojevic Nikola D,Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Stojkovic Tanja,Kostic Vladimir S},
year={2011},
title={Clinical evaluation of DYT6 dystonia in Serbia},
journal={JOURNAL OF NEUROLOGY},
volume={258},
number={},
pages={83-84},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stojkovic Tanja,Svetel Marina V,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S},
year={2011},
title={Cerebellar ataxia and epilepsy caused by hereditary folate malabsorption},
journal={JOURNAL OF NEUROLOGY},
volume={258},
number={},
pages={82-83},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jecmenica-Lukic Milica V,Petrovic Igor N,Dobricic Valerija S,Novakovic Ivana V,Kostic Vladimir S},
year={2010},
title={Exclusion of linkage to chromosome 14q in Serbian family with idiopathic basal ganglia calcification},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={17},
number={},
pages={381-381},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kecmanovic Miljana,Dobricic Valerija S,Dimitrijevic Rajna D,Keckarevic Dusan P,Savic-Pavicevic Dusanka Lj,Keckarevic-Markovic Milica,Ivkovic Maja,Romac Stanka P},
year={2010},
title={Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={120},
number={7},
pages={502-506},
document_type={Article},
} 

@ARTICLE{
author={Dimitrijevic Rajna D,Cadez Ivana,Keckarevic-Markovic Milica,Keckarevic Dusan P,Kecmanovic Miljana,Dobricic Valerija S,Savic-Pavicevic Dusanka Lj,Brajuskovic Goran N,Romac Stanka P},
year={2010},
title={Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={120},
number={7},
pages={496-501},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Dobricic Valerija S,Keckarevic Dusan P,Ignjatovic PM,Romac Stanka P},
year={2008},
title={Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian population},
journal={JOURNAL OF NEUROLOGY},
volume={255},
number={},
pages={102-103},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Jankovic N,Kecmanovic Miljana,Dimitrijevic Rajna D,Keckarevic-Markovic Milica,Dobricic Valerija S,Savic-Pavicevic Dusanka Lj,Romac Stanka P},
year={2008},
title={HD phenocopies - Possible role of saitohin gene},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={118},
number={3},
pages={391-397},
document_type={Article},
} 

@ARTICLE{
author={Djarmati Ana,Dobricic Valerija S,Kecmanovic Miljana,Marsh P,Jancic-Stefanovic Jasna B,Klein Christine,Djuric Milena Lj,Romac Stanka P},
year={2007},
title={MECP2 mutations in Serbian Rett syndrome patients},
journal={ACTA NEUROLOGICA SCANDINAVICA},
volume={116},
number={6},
pages={413-419},
document_type={Editorial Material},
} 

@ARTICLE{
author={Stevanovic Miljana,Dobricic Valerija S,Keckarevic Dusan P,Perovic Aleksandar M,Savic-Pavicevic Dusanka Lj,Keckarevic-Markovic Milica,Jovanovic Aleksandar,Romac Stanka P},
year={2007},
title={Human Y-specific STR haplotypes in population of Serbia and Montenegro},
journal={FORENSIC SCIENCE INTERNATIONAL},
volume={171},
number={2-3},
pages={216-221},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Ercegovac Marko D,Dimitrijevic Rajko N,Dobricic Valerija S,Keckarevic-Markovic Milica,Savic-Pavicevic Dusanka Lj,Keckarevic Dusan P,Saric M,Beslac-Bumbasirevic Ljiljana,Romac Stanka P},
year={2007},
title={Unverricht-Lundborg disease: the first report of genetically confirmed case in Serbia},
journal={JOURNAL OF NEUROLOGY},
volume={254},
number={},
pages={125-125},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Dobricic Valerija S,Kecmanovic Miljana,Dimitrijevic Rajko N,Saric M,Savic-Pavicevic Dusanka Lj,Keckarevic Dusan P,Todorovic Slobodanka,Romac Stanka P},
year={2007},
title={Hereditary motor and sensory neuropathy type Lom in Serbian Romany family},
journal={JOURNAL OF NEUROLOGY},
volume={254},
number={},
pages={109-109},
document_type={Meeting Abstract},
}