@ARTICLE{
author={Fatehi F,Okhovat AA,Nilipour Y,Mroczek M,Straub V,Topf A,Palibrk Aleksa,Peric Stojan Z,Rakocevic-Stojanovic Vidosava M,Najmabadi H,Nafissi S},
year={2020},
title={Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD)},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={27},
number={11},
pages={2257-2266},
document_type={Article},
} 

@ARTICLE{
author={Strehle E,Johnson Katherine,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Farrugia M,Longman C,Straub V},
year={2017},
title={Two novel mutations in the FHL1 gene extending the phenotypic spectrum},
journal={NEUROMUSCULAR DISORDERS},
volume={27},
number={},
pages={S138-S139},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Tonf A,Nikodinovic-Glumac Jelena,Peric Stojan Z,Cassop-Thompson M,Bertoli M,Johnson Katherine,Phillips L,MacArthur D,Rakocevic-Stojanovic Vidosava M,Straub V},
year={2016},
title={A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort},
journal={NEUROMUSCULAR DISORDERS},
volume={26},
number={},
pages={S113-S114},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Johnson Katherine,Bertoli M,Phillips L,Toepf A,Claeys K,Rakocevic-Stojanovic Vidosava M,Peric Stojan Z,Vissine J,Hahn Andreas,Maddison P,Akay E,Bastian A,Lusakowska A,Lek M,Xu L,MacArthur D,Straub V},
year={2016},
title={Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations},
journal={NEUROMUSCULAR DISORDERS},
volume={26},
number={},
pages={S108-S109},
document_type={Meeting Abstract},
}