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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 
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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