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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)

Pediatrics (Evanston), 2007-04, Vol.119 (4), p.e907-e919

2007

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A novel TRPC6 mutation that causes childhood FSGS

PloS one, 2009-11, Vol.4 (11), p.e7771-e7771

2009

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Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

Nephrology, dialysis, transplantation, 2008-04, Vol.23 (4), p.1291-1297

2008

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NPHS3: new clues for understanding idiopathic nephrotic syndrome

Pediatric nephrology (Berlin, West), 2008-06, Vol.23 (6), p.847-850

Hinkes, Bernward G.

2008

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Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome

Pediatric nephrology (Berlin, West), 2008-09, Vol.23 (9), p.1455-1460

2008

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Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome

Pediatric nephrology (Berlin, West), 2007-04, Vol.22 (4), p.509-513

2007

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A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy

BMC nephrology, 2012-05, Vol.13 (1), p.27-27, Article 27

2012

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Childhood pineoblastoma: experiences from the prospective multicenter trials HIT-SKK87, HIT-SKK92 and HIT91

Journal of neuro-oncology, 2007-01, Vol.81 (2), p.217-223

2007

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COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

The Journal of clinical investigation, 2011-05, Vol.121 (5), p.2013-2024

2011

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Long-term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomised multicentre trial HIT'91

European Journal of Cancer, 2009-05, Vol.45 (7), p.1209-1217

2009

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Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome—a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatrische Nephrologie

Pediatric nephrology (Berlin, West), 2008-09, Vol.23 (9), p.1483-1493

2008

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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Nature genetics, 2006-12, Vol.38 (12), p.1397-1405

2006

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Frequency, Risk-Factors and Survival of Children With Atypical Teratoid Rhabdoid Tumors (AT/RT) of the CNS Diagnosed between 1988 and 2004, and Registered to the German HIT Database

Pediatric blood & cancer, 2011-12, Vol.57 (6), p.978-985

2011

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User-Centered Development of an Online Platform for Drug Dosing Recommendations in Pediatrics

Applied clinical informatics, 2019-08, Vol.10 (4), p.570-579

2019

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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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Ependymoma gene expression profiles associated with histological subtype, proliferation, and patient survival

Acta neuropathologica, 2007-03, Vol.113 (3), p.325-337

2007

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“Strawberry wees forever?”: questions

Pediatric nephrology (Berlin, West), 2012-11, Vol.27 (11), p.2049-2050

2012

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“Strawberry wees forever?”: Answers

Pediatric nephrology (Berlin, West), 2012-11, Vol.27 (11), p.2051-2052

2012

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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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Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9

Pediatric research, 2006-02, Vol.59 (2), p.325-331

2006

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Long-term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomised multicentre trial HIT‘91

European journal of cancer (1990), 2009-05, Vol.45 (7), p.1209-1217

2009

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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)

A novel TRPC6 mutation that causes childhood FSGS

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

NPHS3: new clues for understanding idiopathic nephrotic syndrome

Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome

A systematic approach to mapping recessive disease genes in individuals from outbred populations

Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome

A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy

Childhood pineoblastoma: experiences from the prospective multicenter trials HIT-SKK87, HIT-SKK92 and HIT91

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectruma

Long-term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomised multicentre trial HIT'91

Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome—a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatrische Nephrologie

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum

Frequency, Risk-Factors and Survival of Children With Atypical Teratoid Rhabdoid Tumors (AT/RT) of the CNS Diagnosed between 1988 and 2004, and Registered to the German HIT Database

User-Centered Development of an Online Platform for Drug Dosing Recommendations in Pediatrics

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

Ependymoma gene expression profiles associated with histological subtype, proliferation, and patient survival

“Strawberry wees forever?”: questions

“Strawberry wees forever?”: Answers

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

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9

Long-term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomised multicentre trial HIT‘91

Mutations in the human laminin [beta]2 (LAMB2) gene and the associated phenotypic spectruma

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