Maria Szczepanska

Prof.

Medical University of Silesia Faculty of Medical Sciences in Zabrze

Poland

Research Interests

Explore related searches

Professors in Poland Professors in Immunology Immunology professors in Poland

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Professor Maria Szczepanska is a faculty member at the Medical University of Silesia Faculty of Medical Sciences in Zabrze, Poland. Her research focuses on pediatric nephrology, including the assessment of kidney diseases, therapies in childhood cancer, and the genetic basis of renal disorders. Recent publications explore topics such as the clinical challenges of WT1 gene variants, the role of nesfatin-1 in kidney diseases, and the implications of chronic kidney disease in children.

Articles (26)

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Collaborators (25)

Pietro Canetta

Associate Professor of Medicine

Columbia University

UNITED STATES

Maria Szczepanska

Research Interests

Explore related searches

Contact this professor

About

Articles (26)

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

Assessment of eotaxin concentration in children with chronic kidney disease.

Clinical outcomes of pediatric kidney replacement therapy after childhood cancer—An ESPN/ERA Registry study

Early-Start vs. Late-Start Icodextrin for Children Receiving Chronic Peritoneal Dialysis: Findings from the International Pediatric Peritoneal Dialysis Network

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

WT1 Gene Pathogenic Variants: Clinical Challenges and Treatment Strategies in Pediatric Nephrology—One Center Practice

The role of nesfatin-1 in kidney diseases

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

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).

Real-world safety and efficacy of rADAMTS13 in the treatment of congenital thrombotic thrombocytopenic purpura in pediatric patients in Poland.

A Rare De Novo Mutation in the <i>TRIM8</i> Gene in a 17-Year-Old Boy with Steroid-Resistant Nephrotic Syndrome: Case Report

Physical Activity and Its Potential Determinants in Obese Children and Adolescents under Specialist Outpatient Care—A Pilot Cross-Sectional Study

Depressive disorders in children with chronic kidney disease treated conservatively.

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

Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.

Assessment of Interleukin-15 (IL-15) Concentration in Children with Idiopathic Nephrotic Syndrome

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

SARS-CoV-2 Infection as a Possible Trigger for IgA-Associated Vasculitis: A Case Report

The Role of Brain-Derived Neurotrophic Factor (BDNF) in Diagnosis and Treatment of Epilepsy, Depression, Schizophrenia, Anorexia Nervosa and Alzheimer’s Disease as Highly Drug-Resistant Diseases: A Narrative Review

Acquired thrombotic thrombocytopaenic purpura of an atypical, oligosymptomatic course in an adolescent girl

Clinical Characteristics and Courses of Patients With Autosomal Recessive Polycystic Kidney Disease-Mimicking Phenocopies

Pediatric peritoneal dialysis training program and its relationship to peritonitis: a study of the International Pediatric Peritoneal Dialysis Network

Rituximab-associated hypogammaglobulinemia in children with idiopathic nephrotic syndrome: results of an ESPN survey

The Outcome of Childhood Immunoglobulin A Nephropathy with Acute Kidney Injury at the Onset of the Disease-National Study.

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

Collaborators (25)

Pietro Canetta

Marcin Tkaczyk

Yo Han Ahn

Elżbieta Świętochowska

Ruth Loos

Manish Sinha

GIUSEPPE MASNATA

Albert C. M. Ong

Dorota Kamińska

Jordan Nestor

Danuta Zwolinska

Joaquim Calado

ciro esposito

Elisabet Ars

Karolina Rutkowska

Gniewko Więckiewicz

Laureline Berthelot

Hila Milo Rasouly

Zbigniew Heleniak

Agnieszka Książek

Olivia Boyer

Bruno Vogt

Malgorzata Pac

Juan David Gonzalez Rodriguez

Ploski R

Make your next move.