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Kidney International|September 30, 2011
Nephrocalcinosis and urolithiasis in childrenSandra Habbig, Bodo Bernhard Beck, Bernd HoppeExpert Opinion on Investigational Drugs|November 22, 2012
Hyperoxaluria and systemic oxalosis: an update on current therapy and future directionsBodo B Beck, Heike Hoyer-Kuhn, Heike Göbel, et al.Scientific Reports|October 6, 2022
Chronic liver disease and hepatic calcium-oxalate deposition in patients with primary hyperoxaluria type IPia Recker, Bodo Bernhard Beck, Przemyslaw Sikora, et al.Pediatric Nephrology (Berlin, Germany)|February 28, 2012
Enteric hyperoxaluria, recurrent urolithiasis, and systemic oxalosis in patients with Crohn's diseaseRenate Hueppelshaeuser, Gerd E von Unruh, Sandra Habbig, et al.American Journal of Nephrology|May 2, 2009
Renal allograft calcification -- prevalence and etiology in pediatric patientsSandra Habbig, Bodo B Beck, Markus Feldkötter, et al.Pediatric Transplantation|November 20, 2008
Evolution of PTLD following renal transplantation in a childEva Markert, Udo Siebolts, Sandra Habbig, et al.Pediatric Nephrology (Berlin, Germany)|February 1, 2011
Liver fibrosis in recessive multicystic kidney diseases: transient elastography for early detectionSebastian Kummer, Abdurrahman Sagir, Simone Pandey, et al.Blood|August 26, 2009
Platelet-associated complement factor H in healthy persons and patients with atypical HUSChristoph Licht, Fred G Pluthero, Ling Li, et al.Molecular and Cellular Pediatrics|November 7, 2015
Ciliopathies - from rare inherited cystic kidney diseases to basic cellular functionSandra Habbig, Max Christoph LiebauNephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 31, 2012
Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?Bodo B Beck, Sandra Habbig, Katalin Dittrich, et al.Pageof 22