Showing results (71-80 of 108) with videos related to
Sort By:
Pageof 11
Frontiers in Bioscience : a Journal and Virtual Library|September 6, 2003
Diagnostic and therapeutic approaches in patients with secondary hyperoxaluriaBernd Hoppe, Ernst Leumann, Gerd von Unruh, et al.Plos One|June 2, 2016
Quality Assessment of Urinary Stone Analysis: Results of a Multicenter Study of Laboratories in EuropeRoswitha Siener, Noor Buchholz, Michel Daudon, et al.Pediatric Nephrology (Berlin, Germany)|November 23, 2006
Xanthinuria type I: a rare cause of urolithiasisNina Arikyants, Ashot Sarkissian, Albrecht Hesse, et al.Pediatric Nephrology (Berlin, Germany)|March 23, 2005
Hypocitraturia as a risk factor for nephrocalcinosis after kidney transplantationLudwig Stapenhorst, Robert Sassen, Bodo Beck, et al.The Journal of Urology|April 8, 2006
Intestinal oxalate absorption is higher in idiopathic calcium oxalate stone formers than in healthy controls: measurements with the [(13)C2]oxalate absorption testSusanne Voss, Albrecht Hesse, Diana J Zimmermann, et al.Kidney International|May 20, 2003
Hypocitraturia is one of the major risk factors for nephrocalcinosis in very low birth weight (VLBW) infantsPrzemyslaw Sikora, Bernhard Roth, Angela Kribs, et al.World Journal of Urology|November 12, 2005
Oxalate and its handling in a low stone risk vs a stone-prone population groupSonja Lewandowski, Allen L Rodgers, Norbert Laube, et al.Urological Research|March 3, 2004
The population-specific distribution and frequencies of genomic variants in the SLC3A1 and SLC7A9 genes and their application in molecular genetic testing of cystinuriaChrista Schmidt, Udo Vester, Albrecht Hesse, et al.Pediatric Nephrology (Berlin, Germany)|August 16, 2003
Urinary NAG in children with urolithiasis, nephrocalcinosis, or risk of urolithiasisPrzemyslaw Sikora, Sara Glatz, Bodo B Beck, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 1, 2005
Absorptive hyperoxaluria leads to an increased risk for urolithiasis or nephrocalcinosis in cystic fibrosisBernd Hoppe, Gerd E von Unruh, Gesa Blank, et al.Pageof 11