Marcin Zaniew

Zielona Gora, LB, Poland

Last Updated: 09/26/2026

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Found 51 publications

Transient neonatal diabetes mellitus as an early diagnostic clue to HNF1B-related disease - two case reports and a literature review.

Transient neonatal diabetes mellitus as an early diagnostic clue to HNF1B-related disease - two case reports and a literature review.

Journal: Molecular and cellular pediatrics
Published: December 16, 2025

Cinacalcet therapy in symptomatic 11-year-old girl with familial hypocalciuric hypercalcemia type 3.

Cinacalcet therapy in symptomatic 11-year-old girl with familial hypocalciuric hypercalcemia type 3.

Journal: Pediatric nephrology (Berlin, Germany)
Published: October 10, 2025

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Journal: Nature communications
Published: October 09, 2025

FLNA ROD1 and ROD2 Domains are Implicated in Congenital Lower Urinary Tract Obstruction.

FLNA ROD1 and ROD2 Domains are Implicated in Congenital Lower Urinary Tract Obstruction.

Journal: Kidney international reports
Published: December 13, 2024

Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

Journal: Nature communications
Published: November 16, 2024

Assessment of bone status and bone turnover in pediatric patients with familiar hypomagnesemia with hypercalciuria and nephrocalcinosis.

Assessment of bone status and bone turnover in pediatric patients with familiar hypomagnesemia with hypercalciuria and nephrocalcinosis.

Journal: Scientific reports
Published: November 11, 2024

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.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: October 28, 2024

Genome-wide studies define new genetic mechanisms of IgA vasculitis.

Genome-wide studies define new genetic mechanisms of IgA vasculitis.

Journal: medRxiv : the preprint server for health sciences
Published: October 17, 2024

Dent disease: clinical practice recommendations.

Dent disease: clinical practice recommendations.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: September 22, 2024

Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c.

Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c.

Journal: Kidney international
Published: February 20, 2024

Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions.

Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions.

Journal: Kidney international reports
Published: February 13, 2024

Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.

Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.

Journal: Pediatric nephrology (Berlin, Germany)
Published: September 11, 2023
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Last Updated: 09/26/2026