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Pathogenesis, diagnosis and management of hyperkalemia

Pediatric nephrology (Berlin, West), 2011-03, Vol.26 (3), p.377-384

2011

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Diagnostic examination of the child with urolithiasis or nephrocalcinosis

Pediatric nephrology (Berlin, West), 2010-03, Vol.25 (3), p.403-413

2010

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Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study

Journal of the American Society of Nephrology, 2022-06, Vol.33 (6), p.1193-1207

2022

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Both the rituximab dose and maintenance immunosuppression in steroid-dependent/frequently-relapsing nephrotic syndrome have important effects on outcomes

Kidney international, 2020-02, Vol.97 (2), p.393-401

2020

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Human factor H-related protein 2 (CFHR2) regulates complement activation

PloS one, 2013-11, Vol.8 (11), p.e78617-e78617

2013

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New therapies in steroid-sensitive and steroid-resistant idiopathic nephrotic syndrome

Pediatric nephrology (Berlin, West), 2011-06, Vol.26 (6), p.881-892

2011

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Early-Childhood Membranous Nephropathy Due to Cationic Bovine Serum Albumin

The New England journal of medicine, 2011-06, Vol.364 (22), p.2101-2110

2011

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Eculizumab in STEC-HUS: need for a proper randomized controlled trial

Pediatric nephrology (Berlin, West), 2018-08, Vol.33 (8), p.1277-1281

2018

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Difficult-to-treat idiopathic nephrotic syndrome: established drugs, open questions and future options

Pediatric nephrology (Berlin, West), 2018-10, Vol.33 (10), p.1641-1649

2018

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Severe antenatally diagnosed renal disorders: background, prognosis and practical approach

Pediatric nephrology (Berlin, West), 2016-04, Vol.31 (4), p.563-574

2016

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Causes of renal oligohydramnios: impact on prenatal counseling and postnatal outcome

Pediatric nephrology (Berlin, West), 2018-04, Vol.33 (4), p.541-545

2018

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Epidemic Profile of Shiga-Toxin–Producing Escherichia coli O104:H4 Outbreak in Germany

The New England journal of medicine, 2011-11, Vol.365 (19), p.1771-1780

2011

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Chest configuration in children and adolescents with infantile nephropathic cystinosis compared with other chronic kidney disease entities and its clinical determinants

Pediatric nephrology (Berlin, West), 2023-12, Vol.38 (12), p.3989-3999

2023

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Outbreak of hemolytic uremic syndrome caused by E. coli O104:H4 in Germany: a pediatric perspective

Pediatric nephrology (Berlin, West), 2012-02, Vol.27 (2), p.161-164

Kemper, Markus J.

2012

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Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome

Clinical journal of the American Society of Nephrology, 2016-02, Vol.11 (2), p.245-253

2016

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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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Volume expansion mitigates Shiga toxin-producing E. coli-hemolytic uremic syndrome in children

Pediatric nephrology (Berlin, West), 2024-06, Vol.39 (6), p.1901-1907

2024

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Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

Nature genetics, 2016-04, Vol.48 (4), p.457-465

2016

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Hemoconcentration and predictors in Shiga toxin-producing E. coli-hemolytic uremic syndrome (STEC-HUS)

Pediatric nephrology (Berlin, West), 2021-11, Vol.36 (11), p.3777-3783

2021

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Levamisole in relapsing steroid-sensitive nephrotic syndrome: where do we stand?

Kidney international, 2018-02, Vol.93 (2), p.310-313

2018

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Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Nephrology, dialysis, transplantation, 2012-05, Vol.27 (5), p.1729-1736

2012

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Effects of Burosumab Treatment on Mineral Metabolism in Children and Adolescents With X-linked Hypophosphatemia

The journal of clinical endocrinology and metabolism, 2023-09, Vol.108 (10), p.e998-e1006

2023

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Oxalate retinopathy is irreversible despite early combined liver‐kidney transplantation in primary hyperoxaluria type 1

American journal of transplantation, 2019-12, Vol.19 (12), p.3328-3334

2019

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The influence of gender and sexual hormones on incidence and outcome of chronic kidney disease

Pediatric nephrology (Berlin, West), 2012-08, Vol.27 (8), p.1213-1219

2012

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Pathogenesis, diagnosis and management of hyperkalemia

Diagnostic examination of the child with urolithiasis or nephrocalcinosis

Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study

Both the rituximab dose and maintenance immunosuppression in steroid-dependent/frequently-relapsing nephrotic syndrome have important effects on outcomes

Human factor H-related protein 2 (CFHR2) regulates complement activation

New therapies in steroid-sensitive and steroid-resistant idiopathic nephrotic syndrome

Early-Childhood Membranous Nephropathy Due to Cationic Bovine Serum Albumin

Eculizumab in STEC-HUS: need for a proper randomized controlled trial

Difficult-to-treat idiopathic nephrotic syndrome: established drugs, open questions and future options

Severe antenatally diagnosed renal disorders: background, prognosis and practical approach

Causes of renal oligohydramnios: impact on prenatal counseling and postnatal outcome

Epidemic Profile of Shiga-Toxin–Producing Escherichia coli O104:H4 Outbreak in Germany

Chest configuration in children and adolescents with infantile nephropathic cystinosis compared with other chronic kidney disease entities and its clinical determinants

Outbreak of hemolytic uremic syndrome caused by E. coli O104:H4 in Germany: a pediatric perspective

Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome

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

Volume expansion mitigates Shiga toxin-producing E. coli-hemolytic uremic syndrome in children

Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

Hemoconcentration and predictors in Shiga toxin-producing E. coli-hemolytic uremic syndrome (STEC-HUS)

Levamisole in relapsing steroid-sensitive nephrotic syndrome: where do we stand?

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Effects of Burosumab Treatment on Mineral Metabolism in Children and Adolescents With X-linked Hypophosphatemia

Early Effects of Renal Replacement Therapy on Cardiovascular Comorbidity in Children With End-Stage Kidney Disease: Findings From the 4C-T Study

Oxalate retinopathy is irreversible despite early combined liver‐kidney transplantation in primary hyperoxaluria type 1

The influence of gender and sexual hormones on incidence and outcome of chronic kidney disease

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