@ARTICLE{
author={Armirola-Ricaurte Camila,...,Tomic Aleksandra D,...,Milic-Rasic Vedrana M,(broj koautora 20)},
year={2025},
title={Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy},
journal={BRAIN},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@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={Brkusanin Milos,Kosac Ana P,Brankovic-Sreckovic Vesna,Jovanovic Kristina,Karanovic Jelena,Matijasevic-Jokovic Suzana,Garai Nemanja,Pesovic Jovan,Radovanovic Nemanja,Radenkovic Lana,Dobrijevic Zorana Z,Nikolic Dimitrije M,Stevic Zorica D,Brajuskovic Goran N,Milic-Rasic Vedrana M,Savic-Pavicevic Dusanka Lj},
year={2024},
title={Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma in clinically silent and childhood-onset SMA individuals from Serbia},
journal={NEUROMUSCULAR DISORDERS},
volume={43},
number={},
pages={-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Brkusanin Milos,Kosac Ana P,Brankovic-Sreckovic Vesna,Jovanovic Kristina,Peric Stojan Z,Karanovic Jelena,Matijasevic-Jokovic Suzana,Garai Nemanja,Pesovic Jovan,Nikolic Dimitrije M,Stevic Zorica D,Brajuskovic Goran N,Milic-Rasic Vedrana M,Savic-Pavicevic Dusanka Lj},
year={2024},
title={Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma as a Nusinersen treatment response marker in childhood-onset SMA individuals from Serbia},
journal={FRONTIERS IN NEUROLOGY},
volume={15},
number={},
pages={-},
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={Kosac Ana P,Pesovic Jovan,Radenkovic Lana,Brkusanin Milos,Radovanovic Nemanja,Djurisic Marina,Radivojevic Danijela,Mladenovic Jelena M,Ostojic Slavica B,Kovacevic Gordana S,Kravljanac Ruzica M,Savic-Pavicevic Dusanka Lj,Milic-Rasic Vedrana M},
year={2022},
title={LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients},
journal={GENES},
volume={13},
number={8},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Aleksic Dejan Z,Borkovic Milan P,Krivacic Jelena,Petrusic Igor P,Milic-Rasic Vedrana M},
year={2021},
title={Frameshift Mutation in Polar Rich Domain (PRD) of PQBP1 Gene Associated with Asymmetric Cerebellar Hemispheres: A Case Report of Renpenning Syndrome},
journal={IRANIAN JOURNAL OF PEDIATRICS},
volume={31},
number={4},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Beijer Danique,Agnew Thomas,Rack Johannes Gregor Matthias,Prokhorova Evgeniia,Deconinck Tine,Ceulemans Berten,Peric Stojan Z,Milic-Rasic Vedrana M,De Jonghe Peter,Ahel Ivan,Baets Jonathan},
year={2021},
title={Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response},
journal={LIFE SCIENCE ALLIANCE},
volume={4},
number={11},
pages={-},
document_type={Article},
} 

@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={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={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={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={Peric Stojan Z,Nikodinovic-Glumac Jelena,...,Savic-Pavicevic Dusanka Lj,...,Brkusanin Milos,Milenkovic Sanja M,Milic-Rasic Vedrana M,Banko Bojan,Maksimovic Ruzica M,...,Rakocevic-Stojanovic Vidosava M,(broj koautora 19)},
year={2017},
title={A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={25},
number={5},
pages={572-581},
document_type={Article},
} 

@ARTICLE{
author={Atkinson Derek,Nikodinovic-Glumac Jelena,Asselbergh Bob,Ermanoska Biljana,Blocquel David,Steiner Regula,Estrada-Cuzcano Alejandro,Peeters Kristien,Ooms Tinne,De Vriendt Els,Yang Xiang-Lei,Hornemann Thorsten,Milic-Rasic Vedrana M,Jordanova Albena},
year={2017},
title={Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy},
journal={NEUROLOGY},
volume={88},
number={6},
pages={533-542},
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},
} 

@ARTICLE{
author={Atkinson Derek,Asselbergs B,De Vriendt Els,Ooms T,Estrada-Cuzcano A,Nikodinovic Jelena,Milic-Rasic Vedrana M,Jordanova Albena},
year={2016},
title={Compound Heterozygous Mutation in SGPL1 Causes Autosomal Recessive Charcot-Marie-Tooth Disease Type 2 in a Serbian Family},
journal={JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM},
volume={21},
number={3},
pages={233-233},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Gagic Milica,Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P,Mladenovic Jelena M,Dackovic Jelena,Milic-Rasic Vedrana M,Romac Stanka P},
year={2016},
title={Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats},
journal={CLINICAL CHEMISTRY AND LABORATORY MEDICINE},
volume={54},
number={5},
pages={773-780},
document_type={Article},
} 

@ARTICLE{
author={Brkusanin Milos,Kosac Ana P,Jovanovic Vladimir M,Pesovic Jovan,Brajuskovic Goran N,Dimitrijevic Nikola,Todorovic Slobodanka,Romac Stanka P,Milic-Rasic Vedrana M,Savic-Pavicevic Dusanka Lj},
year={2015},
title={Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients},
journal={JOURNAL OF HUMAN GENETICS},
volume={60},
number={11},
pages={723-728},
document_type={Article},
} 

@ARTICLE{
author={Kosac Ana P,Milic-Rasic Vedrana M,Mladenovic Jelena M,Todorovic Slobodanka,Vlahovic Gordana,Rakocevic-Stojanovic Vidosava M,Savic-Pavicevic Dusanka Lj,Lochmuller H},
year={2015},
title={Single referral center study in Serbia: a case series of 41 patients with congenital myasthenic syndromes},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={403-403},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Bladen Catherine L,...,Monges Soledad,Milic-Rasic Vedrana M,Vojinovic Dina,...,(broj koautora 61)},
year={2015},
title={The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations},
journal={HUMAN MUTATION},
volume={36},
number={4},
pages={395-402},
document_type={Article},
} 

@ARTICLE{
author={Milic-Rasic Vedrana M,Vojinovic Dina,Pesovic Jovan,Mijalkovic G,Lukic V,Mladenovic Jelena M,Kosac Ana P,Novakovic Ivana V,Maksimovic Nela S,Romac Stanka P,Todorovic Slobodanka,Pavicevic Savic D},
year={2014},
title={Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={17},
number={2},
pages={25-35},
document_type={Article},
} 

@ARTICLE{
author={Kosac Ana P,Milic-Rasic Vedrana M,Mladenovic Jelena M,Vojinovic Dina,Todorovic Slobodanka},
year={2014},
title={Correctness of referral to the repetitive nerve stimulation test and diagnostic outcome},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={},
pages={S345-S346},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vojinovic Dina,Pesovic Jovan,Savic-Pavicevic Dusanka Lj,Milic-Rasic Vedrana M,Mijalkovic G,Lukic V,Mladenovic Jelena M,Maksimovic N,Todorovic Slobodanka},
year={2014},
title={Intellectual ability in Duchenne muscular dystrophy and dystrophin gene mutation location},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={},
pages={S174-S175},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Cottenie Ellen,...,Milic-Rasic Vedrana M,...,Nikolic Milos MI,...,(broj koautora 40)},
year={2014},
title={Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={95},
number={5},
pages={590-601},
document_type={Article},
} 

@ARTICLE{
author={Balreira Andrea,...,Milic-Rasic Vedrana M,...,(broj koautora 17)},
year={2014},
title={ANO10 mutations cause ataxia and coenzyme Q(10) deficiency},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={11},
pages={2192-2198},
document_type={Article},
} 

@ARTICLE{
author={Kosac Ana P,Milic-Rasic Vedrana M,Mladenovic Jelena M,Vojinovic Dina,Todorovic Slobodanka},
year={2014},
title={Correctness of referral to the repetitive nerve stimulation test and diagnostic outcome},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={21},
number={},
pages={525-525},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Vojinovic Dina,Pesovic Jovan,Savic-Pavicevic Dusanka Lj,Milic-Rasic Vedrana M,Mijalkovic G,Lukic V,Mladenovic Jelena M,Maksimovic N,Todorovic Slobodanka},
year={2014},
title={Intellectual ability in Duchenne muscular dystrophy and dystrophin gene mutation location},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={21},
number={},
pages={255-255},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Bladen Catherine L,...,Milic-Rasic Vedrana M,Kosac Ana P,...,(broj koautora 62)},
year={2014},
title={Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe},
journal={JOURNAL OF NEUROLOGY},
volume={261},
number={1},
pages={152-163},
document_type={Article},
} 

@ARTICLE{
author={Sussman Jon,Argov Zohar,Wirguin Yitzhak,Apolski Slobodan,Milic-Rasic Vedrana M,Soreq Hermona},
year={2013},
title={Further developments with antisense treatment for myasthenia gravis},
journal={MYASTHENIA GRAVIS AND RELATED DISORDERS II},
volume={1275},
number={},
pages={13-16},
document_type={Article},
} 

@ARTICLE{
author={Bladen Catherine L,...,Milic-Rasic Vedrana M,...,(broj koautora 65)},
year={2013},
title={The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia},
journal={HUMAN MUTATION},
volume={34},
number={11},
pages={1449-1457},
document_type={Article},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Dackovic Jelena,Mladenovic Jelena M,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Romac Stanka P},
year={2013},
title={An Algorithm for Genetic Testing of Serbian Patients with Demyelinating Charcot-Marie-Tooth},
journal={GENETIC TESTING AND MOLECULAR BIOMARKERS},
volume={17},
number={1},
pages={85-87},
document_type={Article},
} 

@ARTICLE{
author={Vojinovic Dina,Milic-Rasic Vedrana M},
year={2013},
title={Cognitive impairment of males with Duchenne muscular dystrophy},
journal={JOURNAL OF NEUROLOGY},
volume={260},
number={},
pages={S260-S260},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Zimon Magdalena,...,Nikodinovic Jelena,...,Todorovic Slobodanka,Savic-Pavicevic Dusanka Lj,...,Milic-Rasic Vedrana M,...,(broj koautora 37)},
year={2012},
title={Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia},
journal={NATURE GENETICS},
volume={44},
number={10},
pages={1080-1083},
document_type={Article},
} 

@ARTICLE{
author={Kosac Ana P,Milic-Rasic Vedrana M,Susic Gordana Z,Vojinovic Dina,Todorovic Slobodanka},
year={2012},
title={Neuromuscular disorders and bone mineral density},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={785-785},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Kecmanovic Miljana,Keckarevic Dusan P,Mladenovic Jelena M,Milic-Rasic Vedrana M,Romac Stanka P},
year={2012},
title={A founder R32G mutation in GJB1 gene of Serbian CMT patients},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={783-783},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Nikodinovic Jelena,Milic-Rasic Vedrana M},
year={2012},
title={Clinical presentation in patients with congenital myasthenic syndrome (CMS) due to CHRNE mutations},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={32-32},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mussche Silke,De Paepe Boel,Smet Joel,Devreese Katrien,Lissens Willy,Milic-Rasic Vedrana M,Murnane Matthew,Devreese Bart,Van Coster Rudy},
year={2012},
title={Proteomic Analysis in Giant Axonal Neuropathy: New Insights Into Disease Mechanisms},
journal={MUSCLE & NERVE},
volume={46},
number={2},
pages={246-256},
document_type={Article},
} 

@ARTICLE{
author={Jovanovic Mirjana R,Lakicevic Mira,Stevanovic Dejan S,Milic-Rasic Vedrana M,Slavnic Svetlana S},
year={2012},
title={Community-based study of health-related quality of life in spinal cord injury, muscular dystrophy, multiple sclerosis, and cerebral palsy},
journal={DISABILITY AND REHABILITATION},
volume={34},
number={15},
pages={1284-1290},
document_type={Article},
} 

@ARTICLE{
author={Maksimovic Nela S,Andjelkovic Ana,Milic-Rasic Vedrana M,Rakocevic-Stojanovic Vidosava M,Kastratovic-Kotlica Biljana A,Brankovic Slavko,Damnjanovic Tatjana M,Jekic Biljana B,Bunjevacki Vera I,Lukovic Ljiljana F,Perovic Dijana,Cvjeticanin Suzana,Novakovic Ivana V},
year={2012},
title={Quantitative Analysis of the Dystrophin Gene by Real-Time Pcr},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={64},
number={2},
pages={787-792},
document_type={Article},
} 

@ARTICLE{
author={Mladenovic Jelena M,Milic-Rasic Vedrana M,Keckarevic-Markovic Milica,Romac Stanka P,Todorovic Slobodanka,Rakocevic-Stojanovic Vidosava M,Kisic-Tepavcevic Darija B,Hofman A,Pekmezovic Tatjana D},
year={2011},
title={Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia},
journal={NEUROEPIDEMIOLOGY},
volume={36},
number={3},
pages={177-182},
document_type={Article},
} 

@ARTICLE{
author={Vermeer Sascha,...,Todorovic Slobodanka,Milic-Rasic Vedrana M,...,(broj koautora 30)},
year={2010},
title={Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={87},
number={6},
pages={813-819},
document_type={Article},
} 

@ARTICLE{
author={Potic Ana D,Rovelli Attilio M,Uziel Graziella,Kozic Dusko B,Mladenovic Jelena M,Milic-Rasic Vedrana M},
year={2010},
title={Childhood Cerebral X-Linked Adrenoleukodystrophy More Than 5 Years After Hematopoietic Cell Transplantation: The First Case From Serbia and Southeastern Europe},
journal={JOURNAL OF CHILD NEUROLOGY},
volume={25},
number={12},
pages={1542-1547},
document_type={Article},
} 

@ARTICLE{
author={Baets Jonathan,Deconinck Tine,Smets K,Goossens D,Van den Bergh Peter,Dahan K,Schmedding E,Santens P,Milic-Rasic Vedrana M,Van Damme P,Robberecht Wim,De Meirleir L,Michielsens B,Del-Favero J,Jordanova Albena,De Jonghe Peter},
year={2010},
title={Mutations in SACS cause atypical and late-onset forms of ARSACS},
journal={NEUROLOGY},
volume={75},
number={13},
pages={1181-1188},
document_type={Article},
} 

@ARTICLE{
author={Rakocevic-Stojanovic Vidosava M,Milic-Rasic Vedrana M,Peric Stojan Z,Baets Jonathan,Timmerman Vincent,Dierick Ines,Pavlovic Sanja,De Jonghe Peter},
year={2010},
title={N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={296},
number={1-2},
pages={107-109},
document_type={Article},
} 

@ARTICLE{
author={Mladenovic Jelena M,Milic-Rasic Vedrana M,Mladenovic Jelena M},
year={2010},
title={Comparison of Charcot-Marie-Tooth neuropathy type 2 and type 1A: clinical characteristics},
journal={JOURNAL OF NEUROLOGY},
volume={257},
number={},
pages={P335-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Potic Ana D,Milic-Rasic Vedrana M,Jancic Jasna B},
year={2010},
title={Autoimmune myasthenia gravis: the youngest patient diagnosed in Serbia},
journal={JOURNAL OF NEUROLOGY},
volume={257},
number={},
pages={P322-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Rakocevic-Stojanovic Vidosava M,Milic-Rasic Vedrana M,Van Broeckhoven C,De Jonghe Peter,Nelis Eva,Nikolic Ana V,Tasic Z,Marjanovic Ivan V,Lavrnic Dragana V},
year={2009},
title={Heterozygous missense mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy or silver syndrome},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={285},
number={},
pages={S333-S333},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mladenovic Jelena M,Milic-Rasic Vedrana M,Mladenovic Jelena M},
year={2009},
title={Clinical presentation in patients with axonal Charcot-Marie-Tooth disease (CMT2)},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={16},
number={},
pages={232-232},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Mladenovic Jelena M,Dackovic Jelena,Kecmanovic Miljana,Keckarevic Dusan P,Savic-Pavicevic Dusanka Lj,Romac Stanka P},
year={2009},
title={Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients},
journal={JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM},
volume={14},
number={2},
pages={125-136},
document_type={Article},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Romac Stanka P},
year={2009},
title={Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients},
journal={JOURNAL OF NEUROLOGY},
volume={256},
number={},
pages={S182-S182},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Todorovic Slobodanka,Milic-Rasic Vedrana M,Jovic Nebojsa J,Romac Stanka P},
year={2009},
title={Epilepsy in the population of neuromuscular patients},
journal={EPILEPSIA},
volume={50},
number={},
pages={214-215},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Baumeister Sarah K,Todorovic Slobodanka,Milic-Rasic Vedrana M,Dekomien Gabriele,Lochmueller Hanns,Walter Maggie C},
year={2009},
title={Eosinophilic myositis as presenting symptom in gamma-sarcoglycanopathy},
journal={NEUROMUSCULAR DISORDERS},
volume={19},
number={2},
pages={167-171},
document_type={Article},
} 

@ARTICLE{
author={Potic Ana D,Milic-Rasic Vedrana M,Potic Bojana D},
year={2008},
title={Chronic bilirubin encephalopathy and mental retardation},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={15},
number={},
pages={200-201},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mihaylova Violeta,Mueller Juliane S,Vilchez Juan J,Salih Mustafa A,Kabiraj Mohammad M,D'Amico Adele,Bertini Enrico,Woelfle Joachim,Schreiner Felix,Kurlemann Gerhard,Milic-Rasic Vedrana M,Siskova Dana,Colomer Jaume,Herczegfalvi Agnes,Fabriciova Katarina,Weschke Bernhard,Scola Rosana,Hoellen Friederike,Schara Ulrike,Abicht Angela,Lochmueller Hanns},
year={2008},
title={Phenotypical spectrum of congenital myasthenic syndrome caused by mutations in COLQ gene},
journal={JOURNAL OF NEUROLOGY},
volume={255},
number={},
pages={185-185},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Keckarevic-Markovic Milica,Milic-Rasic Vedrana M,Kecmanovic Miljana,Keckarevic Dusan P,Todorovic Slobodanka,Romac Stanka P},
year={2008},
title={A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease},
journal={JOURNAL OF NEUROLOGY},
volume={255},
number={},
pages={76-77},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Potic Ana D,Milic-Rasic Vedrana M,Mladenovic Jelena M,Potic Bojana D,Kozic Dusko B},
year={2008},
title={Addison's disease as the first manifestation of X-linked adrenoleukodystrophy},
journal={JOURNAL OF NEUROLOGY},
volume={255},
number={},
pages={71-71},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dierick Ines,Baets Jonathan,Irobi Joy,Jacobs An,De Vriendt Els,Deconinck Tine,Merlini Luciano,Van den Bergh Peter,Milic-Rasic Vedrana M,Robberecht Wim,Fischer Dirk,Morales Raul Juntas,Mitrovic Zoran,Seeman Pavel,Mazanec Radim,Kochanski Andrzej,Jordanova Albena,Auer-Grumbach Michaela,Helderman-van den Enden ATJM,Wokke John HJ,Nelis Eva,De Jonghe Peter,Timmerman Vincent},
year={2008},
title={Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study},
journal={BRAIN},
volume={131},
number={},
pages={1217-1227},
document_type={Article},
} 

@ARTICLE{
author={Mihaylova Violeta,Mueller Juliane S,Vilchez Juan J,Salih Mustafa A,Kabiraj Mohammad M,D'Amico Adele,Bertini Enrico,Woelfle Joachim,Schreiner Felix,Kurlemann Gerhard,Milic-Rasic Vedrana M,Siskova Dana,Colomer Jaume,Herczegfalvi Agnes,Fabriciova Katarina,Weschke Bernhard,Scola Rosana,Hoellen Friederike,Schara Ulrike,Abicht Angela,Lochmueller Hanns},
year={2008},
title={Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes},
journal={BRAIN},
volume={131},
number={},
pages={747-759},
document_type={Article},
} 

@ARTICLE{
author={Koop Olga,Schirmacher Anja,Nelis Eva,Timmerman Vincent,De Jonghe Peter,Ringelstein Bernd,Milic-Rasic Vedrana M,Evrard Philippe,Gdrtner Jutta,Claeys Kristl G,Appenzeller Silke,Rautenstrauss Bernd,Hiffine Kathrin,Ramos-Arroyo Maria A,Wrle Helmut,Moilanen Jukka S,HammanS Simon,Kuhlenbdumer Gregor},
year={2007},
title={Genotype-phenotype analysis in patients with giant axonal neuropathy (GAN)},
journal={NEUROMUSCULAR DISORDERS},
volume={17},
number={8},
pages={624-630},
document_type={Article},
} 

@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},
} 

@ARTICLE{
author={Brankovic-Sreckovic Vesna,Milic-Rasic Vedrana M,Djordjevic Valentina J,Kuzmanovic Milos B,Pavlovic Sanja},
year={2007},
title={Arterial ischemic stroke in a child with beta-thalassemia trait and methylentetrahydrofolate reductase mutation},
journal={JOURNAL OF CHILD NEUROLOGY},
volume={22},
number={2},
pages={208-210},
document_type={Article},
} 

@ARTICLE{
author={Mueller Juliane S,Hoellen Friederike,Schara Ulrike,Johannsen J,Bentele K,Rakocevic-Stojanovic Vidosava M,Milic-Rasic Vedrana M,Todorovic Slobodanka,Abicht Angela,Lochmueller Hanns},
year={2006},
title={Novel mutations in the CHRNB1 gene in three patients affected by a congenital myasthenic syndrome},
journal={NEUROMUSCULAR DISORDERS},
volume={16},
number={9-10},
pages={661-661},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mueller Juliane S,Baumeister Sarah K,Milic-Rasic Vedrana M,Krause S,Todorovic Slobodanka,Kugler K,Muller-Felber W,Abicht Angela,Lochmueller Hanns},
year={2006},
title={Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations},
journal={NEUROLOGY},
volume={67},
number={7},
pages={1159-1164},
document_type={Article},
} 

@ARTICLE{
author={Kozic Dusko B,Nagulic Mirjana,Ostojic Jelena V,Samardzic Miroslav M,Milic-Rasic Vedrana M,Skender-Gazibara Milica K,Sener RN},
year={2006},
title={Malignant peripheral nerve sheath tumor of the oculomotor nerve},
journal={ACTA RADIOLOGICA},
volume={47},
number={6},
pages={595-598},
document_type={Article},
} 

@ARTICLE{
author={Parain K,Milic-Rasic Vedrana M,Cabello A,Chinchon I,Illa I,Guicheney P,Richard P,Bertini Enrico,Ferreiro A},
year={2005},
title={Genetic heterogeneity of desmin-related myopathy with Mallory body-like inclusions},
journal={NEUROMUSCULAR DISORDERS},
volume={15},
number={9-10},
pages={694-694},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Brankovic-Sreckovic Vesna,Milic-Rasic Vedrana M,Jovic Nebojsa J,Milic Natasa M,Todorovic Slobodanka},
year={2004},
title={The recurrence risk of ischemic stroke in childhood},
journal={MEDICAL PRINCIPLES AND PRACTICE},
volume={13},
number={3},
pages={153-158},
document_type={Article},
} 

@ARTICLE{
author={Milic-Rasic Vedrana M,Todorovic Slobodanka,Brankovic-Sreckovic Vesna},
year={2004},
title={Problems in prenatal diagnosis of Charcot Marie Tooth type 1},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={11},
number={},
pages={145-145},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Samcovic Andreja,Bojkovic Zoran S,Milic-Rasic Vedrana M},
year={2003},
title={Telemedicine as a new multimedia services: Concepts and advances},
journal={TELSIKS 2003: 6TH INTERNATIONAL CONFERENCE ON TELECOMMUNICATIONS IN MODERN SATELLITE, CABLE AND BROADCASTING SERVICE, VOLS 1 AND 2, PROCEEDINGS OF PAPERS},
volume={},
number={},
pages={399-402},
document_type={Proceedings Paper},
}