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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={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{
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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={Verhoeven K|,Claeys Kristl G|,Zuchner S|,Schroder JM|,Weis J|,Ceuterick C|,Jordanova Albena|,Nelis Eva|,De Vriendt Els|,Van Hul M|,Seeman Pavel|,Mazanec Radim|,Saifi GM|,Szigeti K|,Mancias P|,Butler IJ|,Kochanski Andrzej|,Ryniewicz B|,De Bleecker Jan L|,Van den Bergh Peter|},
year={2006},
title={MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2},
journal={BRAIN},
volume={129},
number={},
pages={2093-2102},
document_type={Article},
} 

