A. Rogowska-Kalisz

Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndrome

F. Anglani, V. Tasic, M. Litwin, 2015, Pediatric Nephrology.

Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort

Se Jin Park, F. Anglani, J. Moczko, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations.

M. Zaniew, M. Szczepańska, M. Konrad, 2015, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Multicenter analysis of the efficacy and safety of a non‐standard immunosuppressive therapy with rituximab in children with steroid‐resistant nephrotic syndrome

M. Tkaczyk, A. Żurowska, D. Drożdż, 2018, Clinical and experimental pharmacology & physiology.

[The results of conservative treatment of oxalate urolithiasis in children].

M. Tkaczyk, M. Nowicki, A. Rogowska-Kalisz, 2003, Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego.

Clinical profile of a Polish cohort of children and young adults with cystinuria

M. Zaniew, M. Tkaczyk, Katarzyna Gadomska-Prokop, 2020, Renal failure.

[Resistance to therapy in primary nephrotic syndrome: effect of MDR1 gene activity].

M. Zaniew, C. Zanker, J. Maciejewski, 2000, Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego.

[Activation of coagulation cascade in children during an idiopathic nephrotic syndrome relapse].

M. Tkaczyk, D. Owczarek, A. Rogowska-Kalisz, 2000, Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego.