@ARTICLE{
author={Dawod Phepy GA,Jancic Jasna B,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Samardzic Janko M,Dawod Ayman Gamil Anwar,Novakovic Ivana V,Abdel Motaleb Fayda I,Radlovic Vladimir N,Kostic Vladimir S,Nikolic Dejan P},
year={2021},
title={Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review},
journal={DIAGNOSTICS},
volume={11},
number={11},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Jankovic Milena Z,Novakovic Ivana V,Dawod Phepy GA,Dawod Ayman Gamil Anwar,Drinic Aleksandra,Motaleb Abdel F,Ducic Sinisa,Nikolic Dejan P},
year={2021},
title={Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis},
journal={INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES},
volume={22},
number={18},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Dawod Phepy GA,Jancic Jasna B,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Samardzic Janko M,Potkonjak Dario,Djuric Vesna,Mesaros Sarlota T,Novakovic Ivana V,Abdel Motaleb Fayda I,Kostic Vladimir S,Nikolic Dejan P},
year={2020},
title={Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy},
journal={GENES},
volume={11},
number={9},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Dawod Phepy GA,Rovcanin Branislav R,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Motaleb Abdel F,Jancic Jasna B,Kostic Vladimir S},
year={2019},
title={Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={1836-1837},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dawod Phepy GA,Rovcanin Branislav R,Marjanovic Ana,Marjanovic Ana,Jankovic Milena Z,Novakovic Ivana V,Dujmovic Irena,Jancic Jasna B,Kostic Vladimir S},
year={2019},
title={Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={181-181},
document_type={Meeting Abstract},
} 

