@ARTICLE{
author={Peco-Antic Amira E,Ivelja Biljana,Milosevski-Lomic Gordana,Paripovic Dusan,Konrad Martin},
year={2018},
title={Hypercalciuria caused by CYP24A1 mutation - fourteen years of the patient's follow-up},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={146},
number={1-2},
pages={77-80},
document_type={Article},
} 

@ARTICLE{
author={Peco-Antic Amira E,Konrad Martin,Milosevski-Lomic Gordana,Dimitrijevic Nikola},
year={2010},
title={Familial Hypomagnesaemia with Hypercalciuria an Nephrocalcinosis: The First Four Patients in Serbia},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={138},
number={5-6},
pages={351-355},
document_type={Article},
} 

@ARTICLE{
author={Konrad Martin,Hou Jianghui,Weber Stefanie,Doetsch Joerg,Kari Jameela A,Seeman Tomas,Kuwertz-Broeking Eberhard,Peco-Antic Amira E,Tasic Velibor,Dittrich Katalin,Alshaya Hammad O,von Vigier Rodo O,Gallati Sabina,Goodenough Daniel A,Schaller Andre},
year={2008},
title={CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis},
journal={JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY},
volume={19},
number={1},
pages={171-181},
document_type={Article},
} 

@ARTICLE{
author={Schonfelder EM,Knuppel T,Tasic Velibor,Miljkovic Predrag,Konrad Martin,Wuhl E,Antignac C,Bakkaloglu A,Schaefer F,Weber Stefanie},
year={2006},
title={Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans},
journal={AMERICAN JOURNAL OF KIDNEY DISEASES},
volume={47},
number={6},
pages={1004-1012},
document_type={Article},
}