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year={2014},
title={Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association},
journal={KIDNEY INTERNATIONAL},
volume={85},
number={6},
pages={1310-1317},
document_type={Article},
} 

@ARTICLE{
author={Bogdanovic Radovan M,Kuburovic Vladimir,Stajic Natasa,Mughal S,Hilger A,Ninic Sanja S,Prijic Sergej M,Ludwig Michael},
year={2012},
title={Liddle syndrome in a Serbian family and literature review of underlying mutations},
journal={EUROPEAN JOURNAL OF PEDIATRICS},
volume={171},
number={3},
pages={471-478},
document_type={Review},
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@ARTICLE{
author={Bogdanovic Radovan M,Kuburovic Vladimir,Stajic Natasa,Mughal S,Hilger A,Kosutic Jovan Lj,Ninic Sanja S,Prijic Sergej M,Vukomanovic Vladislav A,Ludwig Michael},
year={2011},
title={Liddle syndrome: the first family with proven mutation (PRO618SER) in the southeastern Europe},
journal={PEDIATRIC NEPHROLOGY},
volume={26},
number={9},
pages={1717-1717},
document_type={Meeting Abstract},
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@ARTICLE{
author={Bogdanovic Radovan M,Draaken Markus,Toromanovic Alma,Djordjevic Maja S,Stajic Natasa,Ludwig Michael},
year={2010},
title={A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency},
journal={PEDIATRIC NEPHROLOGY},
volume={25},
number={11},
pages={2363-2368},
document_type={Article},
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@ARTICLE{
author={Pavicevic Snezana,Bogdanovic Radovan M,Ludwig Michael,Samardzic Mira P},
year={2008},
title={Dent Disease},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={136},
number={},
pages={312-315},
document_type={Article},
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@ARTICLE{
author={Pavicevic Snezana,Bogdanovic Radovan M,Ludwig Michael},
year={2007},
title={Dent disease - from clinical features to gene analysis},
journal={PEDIATRIC NEPHROLOGY},
volume={22},
number={9},
pages={1498-1498},
document_type={Meeting Abstract},
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