Nephrocalcinosis and urolithiasis in childrenHABBIG, Sandra; BERNHARD BECK, Bodo; HOPPE, Bernd et al.Kidney international. 2011, Vol 80, Num 12, pp 1278-1291, issn 0085-2538, 14 p.Article

The primary hyperoxaluriasHOPPE, Bernd; BECK, Bodo B; MILLINER, Dawn S et al.Kidney international. 2009, Vol 75, Num 12, pp 1264-1271, issn 0085-2538, 8 p.Article

Muscle analysis by measurement of maximal isometric grip force: New reference data and clinical applications in pediatricsRAUCH, Frank; NEU, Christina M; WASSMER, Gernot et al.Pediatric research. 2002, Vol 51, Num 4, pp 505-510, issn 0031-3998Article

Bone mineral content per muscle cross-sectional area as an index of the functional muscle-bone unitSCHOENAU, Eckhard; NEU, Christina Maria; BECK, Bodo et al.Journal of bone and mineral research (Print). 2002, Vol 17, Num 6, pp 1095-1101, issn 0884-0431Article

Detection of polyomavirus BK and JC in children with kidney diseases and renal transplant recipientsMÜLLER, Andreas; BECK, Bodo; THEILEMANN, Kai et al.The Pediatric infectious disease journal. 2005, Vol 24, Num 9, pp 778-781, issn 0891-3668, 4 p.Article

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancyGROSS, Oliver; LICHT, Christoph; KONRAD, Martin et al.Kidney international. 2012, Vol 81, Num 5, pp 494-501, issn 0085-2538, 8 p.Article

C3 deposition glomerulopathy due to a functional Factor H defectHABBIG, Sandra; MIHATSCH, Michael J; HEINEN, Stefan et al.Kidney international. 2009, Vol 75, Num 11, pp 1230-1234, issn 0085-2538, 5 p.Article

Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15LICHT, Christoph; WEYERSBERG, Annic; HEINEN, Stefan et al.American journal of kidney diseases. 2005, Vol 45, Num 2, pp 415-421, issn 0272-6386, 7 p.Article

Reduction of Plasma Oxalate Levels by Oral Application of Oxalobacter formigenes in 2 Patients With Infantile OxalosisHOPPE, Bernd; DITTLICH, Katalin; FEHRENBACH, Henry et al.American journal of kidney diseases. 2011, Vol 58, Num 3, pp 453-455, issn 0272-6386, 3 p.Article

Respiratory and general outcome in neonates with renal oligohydramnios—a single-centre experienceMEHLER, Katrin; BECK, Bodo B; KAUL, Ingrid et al.Nephrology, dialysis, transplantation (Print). 2011, Vol 26, Num 11, pp 3514-3522, issn 0931-0509, 9 p.Article

The Case | A boy with recurrent stonesBECK, Bodo B; LAUBE, Norbert; HABBIG, Sandra et al.Kidney international. 2008, Vol 74, Num 1, pp 133-134, issn 0085-2538, 2 p.Article

Urinary NAG in children with urolithiasis, nephrocalcinosis, or risk of urolithiasisSIKORA, Przemyslaw; GLATZ, Sara; BECK, Bodo B et al.Pediatric nephrology (Berlin, West). 2003, Vol 18, Num 10, pp 996-999, issn 0931-041X, 4 p.Article

Liver cell transplantation in severe infantile oxalosis—a potential bridging procedure to orthotopic liver transplantation?BECK, Bodo B; HABBIG, Sandra; HOPPE, Bernd et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 7, pp 2984-2989, issn 0931-0509, 6 p.Article

Autosomal Dominant Mutation in the Signal Peptide of Renin in a Kindred With Anemia, Hyperuricemia, and CKDBECK, Bodo B; TRACHTMAN, Howard; GITMAN, Michael et al.American journal of kidney diseases. 2011, Vol 58, Num 5, pp 821-825, issn 0272-6386, 5 p.Article

Uromodulin is expressed in renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expressionZAUCKE, Frank; BOEHNLEIN, Joana M; HOPPE, Bernd et al.Human molecular genetics (Print). 2010, Vol 19, Num 10, pp 1985-1997, issn 0964-6906, 13 p.Article