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Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

Kidney international, 2006-09, Vol.70 (6), p.1008-1012

2006

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Unilateral multicystic dysplastic kidney: experience in children

BJU international, 2004-02, Vol.93 (3), p.388-392

2004

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Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD)

Nephrology, dialysis, transplantation, 2009-06, Vol.24 (6), p.1819-1827

2009

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Recurrence of severe steroid dependency in cyclosporin A-treated childhood idiopathic nephrotic syndrome

Nephrology, dialysis, transplantation, 2004-05, Vol.19 (5), p.1136-1141

2004

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Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

Journal of the American Society of Nephrology, 2001-09, Vol.12 (9), p.1872-1881

2001

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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

Journal of the American Society of Nephrology, 2015-06, Vol.26 (6), p.1279-1289

2015

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Central nervous system involvement in hemolytic uremic syndrome (HUS)--a retrospective analysis of cerebral CT and MRI studies

Clinical nephrology, 2001-12, Vol.56 (6), p.S3

2001

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Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiency

Pediatric nephrology (Berlin, West), 2000-06, Vol.14 (6), p.495-498

2000

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Extracorporeal shock wave lithotripsy in children : Efficacy, complications and long-term follow-up

European urology, 2001-05, Vol.39 (5), p.591-597

2001

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Familial hypomagnesemia-hypercalciuria in 2 siblings

Clinical nephrology, 2001-08, Vol.56 (2), p.155

2001

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Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

Kidney international, 1998-06, Vol.53 (6), p.1594-1600

1998

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Neurogenic bladder function disorders in patients with meningomyelocele: S2k guidelines on diagnostics and therapy

Urologe. Ausgabe A, 2015-02, Vol.54 (2), p.239

2015

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Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

Journal of the American Society of Nephrology, 2008-02, Vol.19 (2), p.365-371

2008

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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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High prevalence of febrile urinary tract infections after paediatric renal transplantation

Nephrology, dialysis, transplantation, 2006-11, Vol.21 (11), p.3269-3274

2006

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Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Nephrology, dialysis, transplantation, 2008-11, Vol.23 (11), p.3527-3533

2008

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Intraperitoneal application of low-molecular-weight heparin in continuous ambulatory peritoneal dialysis in a child

Nephron (2015), 2000-12, Vol.86 (4), p.545-545

2000

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Complex malformation: cake kidney with concomitant sacral agenesis

Aktuelle Urologie, 2002-01, Vol.33 (1), p.64-67

2002

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The addition of aminoacids and phosphate to hemodiafiltration solutions in newborns with hyperammonemic coma

Clinical nephrology, 1996-07, Vol.46 (1), p.64

1996

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Urinary tract infections in infants and children -- a consensus on diagnostic, therapy and prophylaxis

Urologe. Ausgabe A, 2007-02, Vol.46 (2), p.112, 114

2007

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Short dialyzed children respond less to growth hormone than patients prior to dialysis

Pediatric nephrology (Berlin, West), 1996-06, Vol.10 (3), p.294-298

1996

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Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease

American journal of kidney diseases, 2006-12, Vol.48 (6), p.942.e1-942.e14

2006

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Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

Unilateral multicystic dysplastic kidney: experience in children

Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD)

Recurrence of severe steroid dependency in cyclosporin A-treated childhood idiopathic nephrotic syndrome

Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

Central nervous system involvement in hemolytic uremic syndrome (HUS)--a retrospective analysis of cerebral CT and MRI studies

Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiency

Extracorporeal shock wave lithotripsy in children : Efficacy, complications and long-term follow-up

Familial hypomagnesemia-hypercalciuria in 2 siblings

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

Neurogenic bladder function disorders in patients with meningomyelocele: S2k guidelines on diagnostics and therapy

Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

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

High prevalence of febrile urinary tract infections after paediatric renal transplantation

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Intraperitoneal application of low-molecular-weight heparin in continuous ambulatory peritoneal dialysis in a child

Complex malformation: cake kidney with concomitant sacral agenesis

The addition of aminoacids and phosphate to hemodiafiltration solutions in newborns with hyperammonemic coma

Urinary tract infections in infants and children -- a consensus on diagnostic, therapy and prophylaxis

Short dialyzed children respond less to growth hormone than patients prior to dialysis

Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease

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