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Journal Article
Tkaczyk, Marcin ORCID: 0000-0003-1753-7560, Gadomska-Prokop, Katarzyna, Zaluska-Lesniewska, Iga, Musial, Kinga
ORCID: 0000-0002-9000-7585, Zawadzki, Jan, Jobs, Katarzyna
ORCID: 0000-0002-8616-2347, Porowski, Tadeusz, Rogowska-Kalisz, Anna, Jander, Anna
ORCID: 0000-0003-1363-091X, Kirolos, Meritrafat, Halinski, Adam
ORCID: 0000-0002-0579-8723, Krzemien, Aleksandra, Sobieszczanska-Drozdziel, Agnieszka, Zachwieja, Katarzyna, Beck, Bodo B., Sikora, Przemyslaw
ORCID: 0000-0002-5698-6863 and Zaniew, Marcin
(2021).
Clinical profile of a Polish cohort of children and young adults with cystinuria.
Ren. Fail., 43 (1).
S. 62 - 71.
ABINGDON:
TAYLOR & FRANCIS LTD.
ISSN 1525-6049
Kolbuc, Marcin, Bienias, Beata, Habbig, Sandra, Kolek, Mateusz F., Szczepanska, Maria ORCID: 0000-0002-6772-1983, Kilis-Pstrusinska, Katarzyna
ORCID: 0000-0001-7352-6992, Wasilewska, Anna, Adamczyk, Piotr, Motyka, Rafal, Tkaczyk, Marcin
ORCID: 0000-0003-1753-7560, Sikora, Przemyslaw
ORCID: 0000-0002-5698-6863, Beck, Bodo B. and Zaniew, Marcin
(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.
J. Clin. Med., 10 (15).
BASEL:
MDPI.
ISSN 2077-0383
Burgmaier, Kathrin, Brinker, Leonie, Erger, Florian, Beck, Bodo B., Benz, Marcus R., Bergmann, Carsten, Boyer, Olivia, Collard, Laure, Dafinger, Claudia, Fila, Marc, Kowalewska, Claudia, Lange-Sperandio, Baerbel, Massella, Laura, Mastrangelo, Antonio, Mekahli, Djalila, Miklaszewska, Monika, Ortiz-Bruechle, Nadina, Patzer, Ludwig, Prikhodina, Larisa, Ranchin, Bruno, Ranguelov, Nadejda, Schild, Raphael, Seeman, Tomas, Sever, Lale, Sikora, Przemyslaw ORCID: 0000-0002-5698-6863, Szczepanska, Maria
ORCID: 0000-0002-6772-1983, Teixeira, Ana, Thumfart, Julia, Uetz, Barbara, Weber, Lutz Thorsten, Wuehl, Elke, Zerres, Klaus, Doetsch, Joerg, Schaefer, Franz and Liebau, Max Christoph
ORCID: 0000-0003-0494-9080
(2021).
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Kidney Int., 100 (3).
S. 650 - 660.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1523-1755