Autori: Konrad Martin
| Naslov | Hypercalciuria caused by CYP24A1 mutation - fourteen years of the patient's follow-up (Article) |
| Autori | Peco-Antic Amira E Ivelja Biljana Milosevski-Lomic Gordana Paripovic Dusan  Konrad Martin
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| Info | SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2018), vol. 146 br. 1-2, str. 77-80 |
| Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [175079] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Familial Hypomagnesaemia with Hypercalciuria an Nephrocalcinosis: The First Four Patients in Serbia (Article) |
| Autori | Peco-Antic Amira E Konrad Martin Milosevski-Lomic Gordana Dimitrijevic Nikola |
| Info | SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2010), vol. 138 br. 5-6, str. 351-355 |
| Projekat | Ministry of Science and Environmental Protection, Government of Serbia [145028] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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| Naslov | CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (Article) |
| Autori | 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 |
| Info | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2008), vol. 19 br. 1 , Suppl. , str. 171 -181 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans (Article) |
| Autori | Schonfelder EM Knuppel T Tasic Velibor Miljkovic Predrag Konrad Martin Wuhl E Antignac C Bakkaloglu A Schaefer F Weber Stefanie |
| Info | AMERICAN JOURNAL OF KIDNEY DISEASES, (2006), vol. 47 br. 6, str. 1004-1012 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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