@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={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={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},
}