The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type IIIHOPPE, Bernd.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 8, pp 3024-3026, issn 0931-0509, 3 p.Article

Diagnostic and therapeutic strategies in hyperoxaluria: a plea for early interventionHOPPE, Bernd; LEUMANN, Ernst.Nephrology, dialysis, transplantation (Print). 2004, Vol 19, Num 1, pp 39-42, issn 0931-0509, 4 p.Article

A United States survey on diagnosis, treatment, and outcome of primary hyperoxaluriaHOPPE, Bernd; LANGMAN, Craig B.Pediatric nephrology (Berlin, West). 2003, Vol 18, Num 10, pp 986-991, issn 0931-041X, 6 p.Article

The primary hyperoxaluriasLEUMANN, Ernst; HOPPE, Bernd.Journal of the American Society of Nephrology. 2001, Vol 12, Num 9, pp 1986-1993, issn 1046-6673Article

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

Posttransplant lymphoproliferative disease in a child: clinical and molecular characterizationLICHT, Christoph; HELL, Karen; EIFINGER, Frank et al.Pediatric nephrology (Berlin, West). 2002, Vol 17, Num 2, pp 79-84, issn 0931-041XArticle

Cardiorespiratory capacity in children and adolescents on maintenance haemodialysisSCHAAR, Bettina; FELDKÖTTER, Markus; NONN, Julia M et al.Nephrology, dialysis, transplantation (Print). 2011, Vol 26, Num 11, pp 3701-3708, issn 0931-0509, 8 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

Evolution of PTLD following renal transplantation in a childMARKERT, Eva; SIEBOLTS, Udo; HABBIG, Sandra et al.Pediatric transplantation. 2009, Vol 13, Num 3, pp 379-383, issn 1397-3142, 5 p.Article

A randomized crossover trial comparing sevelamer with calcium acetate in children with CKDPIEPER, Anne-Kathrin; HAFFNER, Dieter; DÜKER, Gesche et al.American journal of kidney diseases. 2006, Vol 47, Num 4, pp 625-635, issn 0272-6386, 11 p.Article

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatmentCOCHAT, Pierre; HULTON, Sally-Anne; JAMIESON, Neville V et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 5, pp 1729-1736, issn 0931-0509, 8 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

Novel OCRL1 mutations in patients with the phenotype of dent diseaseUTSCH, Boris; BÖKENKAMP, Arend; KUWERTZ-BRÖKING, Eberhard et al.American journal of kidney diseases. 2006, Vol 48, Num 6, pp 942-954, issn 0272-6386, 13 p.Article

Absorptive hyperoxaluria leads to an increased risk for urolithiasis or nephrocalcinosis in cystic fibrosisHOPPE, Bernd; VON UNRUH, Gerd E; BLANK, Gesa et al.American journal of kidney diseases. 2005, Vol 46, Num 3, pp 440-445, issn 0272-6386, 6 p.Article

Hypocitraturia is one of the major risk factors for nephrocalcinosis in very low birth weight (VLBW) infantsSIKORA, Przemyslaw; ROTH, Bernhard; KRIBS, Angela et al.Kidney international. 2003, Vol 63, Num 6, pp 2194-2199, issn 0085-2538, 6 p.Article

Lanthanum Carbonate Inhibits Intestinal Oxalate Absorption and Prevents Nephrocalcinosis After Oxalate Loading in RatsROBIJN, Stef; VERVAET, Benjamin A; HOPPE, Bernd et al.The Journal of urology. 2013, Vol 189, Num 5, pp 1960-1966, issn 0022-5347, 7 p.Article

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9. Commentary : WT1 mutations in steroid-resistant nephrotic syndromeBENZING, Thomas; MUCHA, Bettina; BOGDANOVIC, Radovan et al.Pediatric research. 2006, Vol 59, Num 2, pp 165-166, issn 0031-3998, 9 p.Article

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

Two novel ADAMTS13 gene mutations in thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome (TTP/HUS)LICHT, Christoph; STAPENHORST, Ludwig; SIMON, Thorsten et al.Kidney international. 2004, Vol 66, Num 3, pp 955-958, issn 0085-2538, 4 p.Article

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategyOTTO, Edgar A; RAMASWAMI, Gokul; HOPPE, Bernd et al.Journal of medical genetics. 2011, Vol 48, Num 2, pp 105-116, issn 0022-2593, 12 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

Dent-2 Disease: A Mild Variant of Lowe SyndromeBÖKENKAMP, Arend; BÖCKENHAUER, Detlef; CHEONG, Hae Ii et al.The Journal of pediatrics. 2009, Vol 155, Num 1, pp 94-99, issn 0022-3476, 6 p.Article

Efficacy and Safety of Basiliximab in Pediatric Renal Transplant Patients Receiving Cyclosporine, Mycophenolate Mofetil, and SteroidsOFFNER, Gisela; TOENSHOFF, Burkhard; HOYER, Peter F et al.Transplantation. 2008, Vol 86, Num 9, pp 1241-1248, issn 0041-1337, 8 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