Przemyslaw Sikora

7PUBLICATIONS
45CO-AUTHORS
NeurogeneticsSolid tumoursInfant and child healthMedical bacteriologyNeonatology
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Publications (7)

|Mar 30, 2023
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.

Dina F Ahram, Tze Y Lim, Juntao Ke

|Oct 06, 2022
Chronic liver disease and hepatic calcium-oxalate deposition in patients with primary hyperoxaluria type I.

Pia Recker, Bodo Bernhard Beck, Przemyslaw Sikora

|Oct 13, 2021
The Role of Complement Component C3 Activation in the Clinical Presentation and Prognosis of IgA Nephropathy-A National Study in Children.

Małgorzata Mizerska-Wasiak, Agnieszka Such-Gruchot, Karolina Cichoń-Kawa

|Sep 28, 2021
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO).

Luca M Schierbaum, Sophia Schneider, Stefan Herms

|Aug 07, 2021
Hyperuricemia Is an Early and Relatively Common Feature in Children with HNF1B Nephropathy but Its Utility as a Predictor of the Disease Is Limited.

Marcin Kołbuc, Beata Bieniaś, Sandra Habbig

|Feb 18, 2021
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina

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Frequent Collaborators

3 joint publications

Monika Miklaszewska

3 joint publications

Marcin Tkaczyk

2 joint publications

Maddalena Marasà

2 joint publications

Maria Szczepanska