@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={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={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={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},
}