Beata Leszczynska
Warsaw, MZ, Poland
Last Updated: 09/26/2026
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Found 25 publications
Suppressor of cytokine signaling 2 is associated with growth impairment in pediatric chronic kidney disease.
Journal: Pediatric nephrology (Berlin, Germany)
Published: July 06, 2025
Changing Epidemiology and Outcomes of Hemolytic Uremic Syndrome in Children: A Prospective National Cohort Study from the Polish Pediatric HUS Registry and the Polish Registry of Renal Replacement Therapy in Children.
Journal: Journal of clinical medicine
Published: September 23, 2024
Haemolytic uremic syndrome as a cause of chronic kidney disease stage 5 in children is in retreat: results from the Polish Registry of Kidney Replacement Therapy in children (2000-2023).
Journal: Pediatric nephrology (Berlin, Germany)
Published: August 05, 2024
Epidemiological Characteristics of Shiga Toxin-Producing Escherichia coli Responsible for Infections in the Polish Pediatric Population.
Journal: Polish journal of microbiology
Published: May 10, 2024
The usefulness of urinary netrin-1 determination as an early marker of acute kidney injury in children after cardiac surgery.
Journal: Archives of medical science : AMS
Published: March 03, 2024
Depressive disorders in children with chronic kidney disease treated conservatively.
Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University
Published: September 04, 2023
Associations of longitudinal height and weight with clinical outcomes in pediatric kidney replacement therapy: results from the ESPN/ERA Registry.
Journal: Pediatric nephrology (Berlin, Germany)
Published: January 23, 2023
Compound Haplotype Variants in CFH and CD46 Genes Determine Clinical Outcome of Atypical Hemolytic Uremic Syndrome (aHUS)-A Series of Cases from a Single Family.
Journal: Journal of personalized medicine
Published: March 26, 2021
Treatment of idiopathic nephrotic syndrome with two steroid dosing regimens - one-year observational study.
Journal: Central-European journal of immunology
Published: February 11, 2021
Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35.
Journal: American journal of medical genetics. Part A
Published: March 30, 2020
Life activity, disease acceptance and quality of life in patients treated with renal replacement therapy since childhood.
Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University
Published: April 11, 2019
Last Updated: 09/26/2026