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TLR2 mediates renal apoptosis in neonatal mice subjected experimentally to obstructive nephropathy

PloS one, 2023-11, Vol.18 (11), p.e0294142-e0294142

2023

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Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease

Journal of the American Society of Nephrology, 2011-11, Vol.22 (11), p.2047-2056

2011

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2 Monate/m mit Trinkschwäche und Fieber: Vorbereitung auf die Facharztprüfung: Fall 8

Monatsschrift Kinderheilkunde, 2021-09, Vol.169 (Suppl 4), p.243-247

Benz, Marcus

2021

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Not all farming environments protect against the development of asthma and wheeze in children

Journal of allergy and clinical immunology, 2007-05, Vol.119 (5), p.1140-1147

2007

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Idiopathisches nephrotisches Syndrom im Kindesalter

Monatsschrift Kinderheilkunde, 2024, Vol.172 (6), p.543-555

Benz, Marcus R.

2024

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Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency

Kidney international, 2022-09, Vol.102 (3), p.604-612

2022

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Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy

Kidney international, 2022-09, Vol.102 (3), p.592-603

2022

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Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy —short version of the updated German best practice guideline (S2e) — AWMF register no. 166-001, 6/2020

Pediatric nephrology (Berlin, West), 2021-10, Vol.36 (10), p.2971-2985

2021

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Prenatal farm exposure is related to the expression of receptors of the innate immunity and to atopic sensitization in school-age children

Journal of Allergy and Clinical Immunology, 2006-04, Vol.117 (4), p.817-823

2006

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Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1

Clinical journal of the American Society of Nephrology, 2015-05, Vol.10 (5), p.825-831

2015

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Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

The Journal of clinical investigation, 2022-06, Vol.132 (11)

2022

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Commentary on “Pediatric Idiopathic Steroid-sensitive Nephrotic Syndrome Diagnosis and Therapy - Short version of the updated German Best Practice Guideline (S2e)”

Pediatric nephrology (Berlin, West), 2021-10, Vol.36 (10), p.2961-2966

2021

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Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy

Pediatric nephrology (Berlin, West), 2016-06, Vol.31 (6), p.941-955

2016

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Initial treatment of steroid-sensitive idiopathic nephrotic syndrome in children with mycophenolate mofetil versus prednisone: protocol for a randomised, controlled, multicentre trial (INTENT study)

BMJ open, 2018-10, Vol.8 (10), p.e024882-e024882

2018

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Reply to correspondence letter by A. Costa et al.: pediatric mercury poisoning, brain MRI, and white matter hyperintensities

European journal of pediatrics, 2011-05, Vol.170 (5), p.679-679

Benz, Marcus R.

2011

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Hyperintense lesions in brain MRI after exposure to a mercuric chloride-containing skin whitening cream

European journal of pediatrics, 2011-06, Vol.170 (6), p.747-750

2011

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Humic Acid Reduction by Propionibacterium freudenreichii and Other Fermenting Bacteria

Applied and Environmental Microbiology, 1998-11, Vol.64 (11), p.4507-4512

1998

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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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No Impact of the Analytical Method Used for Determining Cystatin C on Estimating Glomerular Filtration Rate in Children

Frontiers in pediatrics, 2017-04, Vol.5, p.66-66

2017

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Novel heterozygous COL4A3 mutation in a family with late-onset ESRD

Pediatric nephrology (Berlin, West), 2010-08, Vol.25 (8), p.1539-1542

2010

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Different factor H-related protein patterns in siblings with typical hemolytic uremic syndrome

Pediatric nephrology (Berlin, West), 2011-08, Vol.26 (8), p.1345-1347

2011

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Electron shuttling via humic acids in microbial iron(III) reduction in a freshwater sediment

FEMS microbiology ecology, 2004-01, Vol.47 (1), p.85-92

2004

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Klinikleitfaden Padiatrie

2017

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Reduced methotrexate clearance and renal impairment in a boy with osteosarcoma and earlier undetected autosomal dominant polycystic kidney disease (ADPKD)

Journal of pediatric hematology/oncology, 2010-11, Vol.32 (8), p.e314-e316

2010

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Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy -short version of the updated German best practice guideline

Pediatric nephrology (Berlin, West), 2021-10, Vol.36 (10), p.2971

2021

Volltextzugriff (PDF)

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TLR2 mediates renal apoptosis in neonatal mice subjected experimentally to obstructive nephropathy

Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease

2 Monate/m mit Trinkschwäche und Fieber: Vorbereitung auf die Facharztprüfung: Fall 8

Not all farming environments protect against the development of asthma and wheeze in children

Idiopathisches nephrotisches Syndrom im Kindesalter

Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency

Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy

Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy —short version of the updated German best practice guideline (S2e) — AWMF register no. 166-001, 6/2020

Prenatal farm exposure is related to the expression of receptors of the innate immunity and to atopic sensitization in school-age children

Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

Commentary on “Pediatric Idiopathic Steroid-sensitive Nephrotic Syndrome Diagnosis and Therapy - Short version of the updated German Best Practice Guideline (S2e)”

Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy

Initial treatment of steroid-sensitive idiopathic nephrotic syndrome in children with mycophenolate mofetil versus prednisone: protocol for a randomised, controlled, multicentre trial (INTENT study)

Reply to correspondence letter by A. Costa et al.: pediatric mercury poisoning, brain MRI, and white matter hyperintensities

Hyperintense lesions in brain MRI after exposure to a mercuric chloride-containing skin whitening cream

Humic Acid Reduction by Propionibacterium freudenreichii and Other Fermenting Bacteria

Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease

No Impact of the Analytical Method Used for Determining Cystatin C on Estimating Glomerular Filtration Rate in Children

Novel heterozygous COL4A3 mutation in a family with late-onset ESRD

Different factor H-related protein patterns in siblings with typical hemolytic uremic syndrome

Electron shuttling via humic acids in microbial iron(III) reduction in a freshwater sediment

Klinikleitfaden Padiatrie

Reduced methotrexate clearance and renal impairment in a boy with osteosarcoma and earlier undetected autosomal dominant polycystic kidney disease (ADPKD)

Pediatric idiopathic steroid-sensitive nephrotic syndrome: diagnosis and therapy -short version of the updated German best practice guideline

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