@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={Oury Julien,Liu Yun,Topf Ana,Todorovic Slobodanka,Hoedt Esthelle,Preethish-Kumar Veeramani,Neubert Thomas A,Lin Weichun,Lochmueller Hanns,Burden Steven J},
year={2019},
title={MACF1 links Rapsyn to microtubule- and actin-binding proteins to maintain neuromuscular synapses},
journal={JOURNAL OF CELL BIOLOGY},
volume={218},
number={5},
pages={1686-1705},
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={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={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={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={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={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={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={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={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={Mladenovic Jelena M,Pekmezovic Tatjana D,Todorovic Slobodanka,Rakocevic-Stojanovic Vidosava M,Savic Dusanka Lj,Romac Stanka P,Apostolski Slobodan A},
year={2006},
title={Epidemiology of myotonic dystrophy type 1 (Steinert disease) in Belgrade (Serbia)},
journal={CLINICAL NEUROLOGY AND NEUROSURGERY},
volume={108},
number={8},
pages={757-760},
document_type={Article},
} 

@ARTICLE{
author={Savic Dusanka Lj,Keckarevic Dusan P,Brankovic-Sreckovic Vesna,Apostolski Slobodan A,Todorovic Slobodanka,Romac Stanka P},
year={2006},
title={Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history},
journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE},
volume={116},
number={12},
pages={1509-1518},
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={Mladenovic Jelena M,Pekmezovic Tatjana D,Todorovic Slobodanka,Rakocevic-Stojanovic Vidosava M,Savic Dusanka Lj,Romac Stanka P,Apostolski Slobodan A},
year={2006},
title={Survival and mortality of myotonic dystrophy type 1 (Steinert's disease) in the population of Belgrade},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={13},
number={5},
pages={451-454},
document_type={Article},
} 

@ARTICLE{
author={Todorovic Slobodanka},
year={2005},
title={Therapeutics strategetics in juvenile myasthenia gravis},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={238},
number={},
pages={S177-S177},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Novakovic Ivana V,Bojic Daniela Z,Todorovic Slobodanka,Apostolski Slobodan A,Lukovic Ljiljana F,Stefanovic D,Milasin Jelena M},
year={2005},
title={Proximal dystrophin gene deletions and protein alterations in Becker muscular dystrophy},
journal={BIOPHYSICS FROM MOLECULES TO BRAIN: IN MEMORY OF RADOSLAV K. ANDJUS},
volume={1048},
number={},
pages={406-410},
document_type={Article},
} 

@ARTICLE{
author={Krndija D,Savic Dusanka Lj,Mladenovic Jelena M,Rakocevic-Stojanovic Vidosava M,Apostolski Slobodan A,Todorovic Slobodanka,Romac Stanka P},
year={2005},
title={Haplotype analysis of the DM1 locus in the Serbian population},
journal={ACTA NEUROLOGICA SCANDINAVICA},
volume={111},
number={4},
pages={274-277},
document_type={Article},
} 

@ARTICLE{
author={Cosic NC,Gligorovic S,Jovic Nebojsa J,Todorovic Slobodanka},
year={2004},
title={The clinical significance of seizures in newborns weighing less than 2500 grams},
journal={EPILEPSIA},
volume={45},
number={},
pages={192-192},
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={Cosic NC,Prostran Milica S,Jovic Nebojsa J,Gligorovic S,Todorovic Slobodanka},
year={2003},
title={Neurological development of infants exposed to benzodiazepines in utero},
journal={EUROPEAN NEUROPSYCHOPHARMACOLOGY},
volume={13},
number={},
pages={S408-S409},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Novakovic Ivana V,Apostolski Slobodan A,Todorovic Slobodanka,Lukovic Ljiljana F,Bunjevacki Vera I,Bojic Daniela Z,Mestroni L,Milasin Jelena M},
year={2002},
title={Cardiac disorders in BMD patients with distal gene deletions},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={10},
number={},
pages={257-257},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Savic Dusanka Lj,Rakocevic-Stojanovic Vidosava M,Keckarevic Dusan P,Culjkovic Biljana,Stojkovic O,Mladenovic Jelena M,Todorovic Slobodanka,Apostolski Slobodan A,Romac Stanka P},
year={2002},
title={250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1},
journal={HUMAN MUTATION},
volume={19},
number={2},
pages={131-139},
document_type={Article},
} 

@ARTICLE{
author={Savic Dusanka Lj,Topisirovic Ivan,Keckarevic-Markovic Milica,Keckarevic Dusan P,Major Tamara,Culjkovic Biljana,Stojkovic O,Rakocevic-Stojanovic Vidosava M,Mladenovic Jelena M,Todorovic Slobodanka,Apostolski Slobodan A,Romac Stanka P},
year={2001},
title={Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?},
journal={PSYCHIATRIC GENETICS},
volume={11},
number={4},
pages={201-205},
document_type={Article},
}