Grazyna J. Krzemien

Warsaw, MZ, Poland

Last Updated: 09/26/2026

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Found 46 publications

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

Atypical Liver Ultrasound Image in a Boy with Autosomal Recessive Polycystic Kidney Disease (ARPKD) and New PKD1 Variant-A Case Report.

Atypical Liver Ultrasound Image in a Boy with Autosomal Recessive Polycystic Kidney Disease (ARPKD) and New PKD1 Variant-A Case Report.

Journal: Genes
Published: October 02, 2025

Total Kidney Volume, Hypertension, and Deterioration of Kidney Function in Children with Early-Stage ADPKD.

Total Kidney Volume, Hypertension, and Deterioration of Kidney Function in Children with Early-Stage ADPKD.

Journal: Journal of clinical medicine
Published: May 21, 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

Antibiotic Prophylaxis in Infants with Grade III, IV, or V Vesicoureteral Reflux.

Antibiotic Prophylaxis in Infants with Grade III, IV, or V Vesicoureteral Reflux.

Journal: The New England journal of medicine
Published: September 13, 2023

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.

Journal: Journal of the American Society of Nephrology : JASN
Published: September 24, 2022

Genome-wide association study in patients with posterior urethral valves.

Genome-wide association study in patients with posterior urethral valves.

Journal: Frontiers in pediatrics
Published: July 07, 2022

Serum and urine periostin and cytokeratin-18 in children with congenital obstructive nephropathy.

Serum and urine periostin and cytokeratin-18 in children with congenital obstructive nephropathy.

Journal: Central-European journal of immunology
Published: February 12, 2022

Serum neutrophil gelatinase-associated lipocalin for predicting anemia of inflammation in children with urinary tract infection.

Serum neutrophil gelatinase-associated lipocalin for predicting anemia of inflammation in children with urinary tract infection.

Journal: Central-European journal of immunology
Published: November 15, 2021

The Usefulness of Urinary Periostin, Cytokeratin-18, and Endoglin for Diagnosing Renal Fibrosis in Children with Congenital Obstructive Nephropathy.

The Usefulness of Urinary Periostin, Cytokeratin-18, and Endoglin for Diagnosing Renal Fibrosis in Children with Congenital Obstructive Nephropathy.

Journal: Journal of clinical medicine
Published: September 19, 2021

Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO).

Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO).

Journal: Genes
Published: August 01, 2021
Showing 1-12 of 46

Last Updated: 09/26/2026