Marcus R. Benz

Mycophenolate dosing in childhood nephrotic syndrome - Authors' reply.

Journal: The Lancet. Child & adolescent health

Published: May 18, 2026

Mycophenolate mofetil versus prednisone for the initial treatment of idiopathic steroid-sensitive nephrotic syndrome in children in Germany (INTENT): a multicentre, open-label, randomised, controlled, parallel-group, non-inferiority, phase 3 trial.

Journal: The Lancet. Child & adolescent health

Published: July 30, 2025

A novel, dominant disease mechanism of distal renal tubular acidosis with specific variants in ATP6V1B1.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: October 28, 2024

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

Journal: PloS one

Published: April 21, 2023

Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosis.

Journal: Molecular genetics and metabolism

Published: June 26, 2022

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

Journal: The Journal of clinical investigation

Published: June 01, 2022

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

Journal: Kidney international

Published: February 19, 2022

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

Journal: Kidney international

Published: September 09, 2021

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

Journal: Pediatric nephrology (Berlin, Germany)

Published: April 28, 2021

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.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 28, 2021

Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.

Journal: Kidney international

Published: August 14, 2020

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.

Journal: American journal of human genetics

Published: July 27, 2020

Mycophenolate dosing in childhood nephrotic syndrome - Authors' reply.

Mycophenolate dosing in childhood nephrotic syndrome - Authors' reply.

Mycophenolate mofetil versus prednisone for the initial treatment of idiopathic steroid-sensitive nephrotic syndrome in children in Germany (INTENT): a multicentre, open-label, randomised, controlled, parallel-group, non-inferiority, phase 3 trial.

Mycophenolate mofetil versus prednisone for the initial treatment of idiopathic steroid-sensitive nephrotic syndrome in children in Germany (INTENT): a multicentre, open-label, randomised, controlled, parallel-group, non-inferiority, phase 3 trial.

A novel, dominant disease mechanism of distal renal tubular acidosis with specific variants in ATP6V1B1.

A novel, dominant disease mechanism of distal renal tubular acidosis with specific variants in ATP6V1B1.

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

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

Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosis.

Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosis.

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

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

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

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.

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

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

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

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 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.

Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.

Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.

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

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