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Journal of Pediatric Urology|June 22, 2017
Evaluation of the effect of 3-month bladder basic advice in children with monosymptomatic nocturnal enuresisMarcin Tkaczyk, Michał Maternik, Anna Krakowska, et al.
Developmental Period Medicine|September 4, 2014
Serum fibroblast growth factor 23 and calcium-phosphorus metabolism parameters in children with chronic kidney disease - preliminary reportHelena Ziółkowska, Magdalena Okarska-Napierała, Anna Stelmaszczyk-Emmel, et al.
Nephron|May 24, 2018
A de novo KCNA1 Mutation in a Patient with Tetany and HypomagnesemiaJenny van der Wijst, Martin Konrad, Sjoerd A J Verkaart, et al.
Ginekologia Polska|August 9, 2019
Neonatal survival and kidney function after prenatal interventions for obstructive uropathiesMarcin Tkaczyk, Malgorzata Stanczyk, Waldemar Krzeszowski, et al.
Journal of Clinical Medicine|August 7, 2021
Hyperuricemia Is an Early and Relatively Common Feature in Children with HNF1B Nephropathy but Its Utility as a Predictor of the Disease Is LimitedMarcin Kołbuc, Beata Bieniaś, Sandra Habbig, et al.
Advances in Medical Sciences|October 27, 2015
Growth and nutritional status in children with chronic kidney disease on maintenance dialysis in PolandMałgorzata Stańczyk, Monika Miklaszewska, Katarzyna Zachwieja, et al.
Archives of Medical Science : AMS|February 29, 2012
Successes and pitfalls of chronic peritoneal dialysis in infants - a Polish nationwide outcome studyAnna Jander, Irena Makulska, Joanna Latoszyńska, et al.
European Journal of Pediatrics|October 26, 2010
Polish 2010 growth references for school-aged children and adolescentsZbigniew Kułaga, Mieczysław Litwin, Marcin Tkaczyk, et al.
Renal Failure|November 25, 2016
What has changed in the prevalence of hypertension in dialyzed children during the last decade?Marcin Tkaczyk, Małgorzata Stańczyk, Monika Miklaszewska, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 6, 2014
Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutationsPrzemysław Sikora, Marcin Zaniew, Lea Haisch, et al.
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