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Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome

Clinical journal of the American Society of Nephrology, 2013-03, Vol.8 (3), p.407-415

2013

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No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria

BMC nephrology, 2018-10, Vol.19 (1), p.278-278, Article 278

2018

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Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome

Clinical journal of the American Society of Nephrology, 2009-08, Vol.4 (8), p.1312-1316

2009

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Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes

Pediatric nephrology (Berlin, West), 2014-10, Vol.29 (10), p.1915-1925

2014

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Primärer Megaureter beim Neugeborenen – die passagere externe Harnableitung – ein Plädoyer

Aktuelle Urologie, 2020-04, Vol.51 (2), p.132-136

2020

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Etiology of Kidney Diseases With Proteinuria in the Gambia/West Africa

Frontiers in pediatrics, 2022-03, Vol.10, p.854719-854719

2022

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Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo

Scientific reports, 2018-04, Vol.8 (1), p.6003-1, Article 6003

2018

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Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis

Respiratory research, 2006-06, Vol.7 (1), p.87-87, Article 87

2006

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Young Man With Kidney Failure and Hemorrhagic Interstitial Nephritis

American journal of kidney diseases, 2009-12, Vol.54 (6), p.1162-1166

2009

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Eculizumab for Atypical Hemolytic–Uremic Syndrome

The New England journal of medicine, 2009-01, Vol.360 (5), p.542-544

2009

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Nierenzysten und zystische Nierenerkrankungen bei Kindern (AWMF S2k-Leitlinie)

Klinische Pädiatrie, 2020-09, Vol.232 (5), p.228-248

2020

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Primary megaureter in the newborn period: making the case for a temporary splint-free cutaneous ureterostomy

Aktuelle Urologie, 2020-04, Vol.51 (2), p.132

2020

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Cyclophosphamide in steroid-sensitive nephrotic syndrome: outcome and outlook

Pediatric nephrology (Berlin, West), 2003-07, Vol.18 (7), p.661-664

2003

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An Outbreak of Shiga Toxin—Producing Escherichia coli O104:H4 Hemolytic Uremic Syndrome in Germany: Presentation and Short-term Outcome in Children

Clinical infectious diseases, 2012-09, Vol.55 (6), p.753-759

2012

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HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry

Pediatric nephrology (Berlin, West), 2019-06, Vol.34 (6), p.1065-1075

2019

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Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4

Clinical infectious diseases, 2017-06, Vol.64 (12), p.1637-1643

2017

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DEAP-HUS: Deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome

Pediatric nephrology (Berlin, West), 2010-10, Vol.25 (10), p.2009-2019

2010

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Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

Kidney international, 2014-04, Vol.85 (4), p.880-887

2014

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Combined liver and kidney transplantation and kidney after liver transplantation in children: Indication, postoperative outcome, and long-term results

Pediatric transplantation, 2015-12, Vol.19 (8), p.858-865

2015

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The diagnostic value of ultrasound in cystic kidney diseases

Pediatric nephrology (Berlin, West), 2010-02, Vol.25 (2), p.231-240

2010

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Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo

Scientific reports, 2017-11, Vol.7 (1), p.14554-11, Article 14554

2017

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Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

Kidney international, 2005-03, Vol.67 (3), p.829-848

2005

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Everolimus: A Viewpoint by Udo Vester

Drugs (New York, N.Y.), 2004-04, Vol.64 (8), p.873-874

Vester, Udo

2004

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Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathy

Scientific reports, 2016-08, Vol.6 (1), p.31992-31992, Article 31992

2016

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Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease

Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic Syndrome

No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria

Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes

Primärer Megaureter beim Neugeborenen – die passagere externe Harnableitung – ein Plädoyer

Etiology of Kidney Diseases With Proteinuria in the Gambia/West Africa

Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo

Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis

Young Man With Kidney Failure and Hemorrhagic Interstitial Nephritis

Eculizumab for Atypical Hemolytic–Uremic Syndrome

Nierenzysten und zystische Nierenerkrankungen bei Kindern (AWMF S2k-Leitlinie)

Primary megaureter in the newborn period: making the case for a temporary splint-free cutaneous ureterostomy

Cyclophosphamide in steroid-sensitive nephrotic syndrome: outcome and outlook

An Outbreak of Shiga Toxin—Producing Escherichia coli O104:H4 Hemolytic Uremic Syndrome in Germany: Presentation and Short-term Outcome in Children

HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry

Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4

DEAP-HUS: Deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome

Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

Combined liver and kidney transplantation and kidney after liver transplantation in children: Indication, postoperative outcome, and long-term results

The diagnostic value of ultrasound in cystic kidney diseases

Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo

Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD)

Everolimus: A Viewpoint by Udo Vester

Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathy

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