Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kacper Wasielewski"'
Autor:
Maria Szczepańska, Joanna Ksiazek, Mieczysław Litwin, Beata S. Lipska, Marcin Tkaczyk, Elzbieta Kuzma-Mroczkowska, Aleksandra Zurowska, Janusz Limon, Magdalena Silska, Anna Medyńska, Anna Wasilewska, Franz Schaefer, L Morzuch, Tomasz Jarmoliński, Kacper Wasielewski, Irena Bałasz-Chmielewska, Halina Borzecka, Agnieszka Firszt-Adamczyk, Ewa Gacka, Dorota Drozdz, Dominika Vetter
Publikováno v:
Journal of Applied Genetics; Vol 54
Journal of Applied Genetics
Journal of Applied Genetics
Hereditary nephrotic syndrome is caused by mutations in a number of different genes, the most common being NPHS2. The aim of the study was to identify the spectrum of NPHS2 mutations in Polish patients with the disease. A total of 141 children with s
Autor:
Elżbieta Bylina, Iwona Ługowska, Kacper Wasielewski, Urszula Grzesiakowska, Zbigniew Nowecki, Czesław Osuch, Piotr Rutkowski, Anna Klimczak, Janusz Limon, Ewa Mierzejewska, Janusz A. Siedlecki, Tomasz Świtaj, Agnieszka Woźniak, Sławomir Falkowski, Magdalena Brzeskwiniewicz, Wojciech Melerowicz, J. Kroc
Publikováno v:
BMC Cancer
BMC Cancer, Vol 12, Iss 1, p 107 (2012)
BMC Cancer, Vol 12, Iss 1, p 107 (2012)
Background Gastrointestinal stromal tumors (GIST) mutational status is recognized factor related to the results of tyrosine kinase inhibitors therapy such as imatinib (IM) or sunitinib (SU). Arterial hypertension (AH) is common adverse event related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90c408b1f8119f696eff7f664e15dcb
https://ruj.uj.edu.pl/xmlui/handle/item/154877
https://ruj.uj.edu.pl/xmlui/handle/item/154877