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Page 1
The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, Mitrotti A, Fasel DA, Batourina E, Sampson MG, Bodria M, Werth M, Kao C, Martino J, Capone VP, Vivante A, Shril S, Kil BH, Marasà M, Zhang JY, Na YJ, Lim TY, Ahram D, Weng PL, Heinzen EL, Carrea A, Piaggio G, Gesualdo L, Manca V, Masnata G, Gigante M, Cusi D, Izzi C, Scolari F, van Wijk JAE, Saraga M, Santoro D, Conti G, Zamboli P, White H, Drozdz D, Zachwieja K, Miklaszewska M, Tkaczyk M, Tomczyk D, Krakowska A, Sikora P, Jarmoliński T, Borszewska-Kornacka MK, Pawluch R, Szczepanska M, Adamczyk P, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Dobson MG, Darlow JM, Puri P, Barton DE, Furth SL, Warady BA, Gucev Z, Lozanovski VJ, Tasic V, Pisani I, Allegri L, Rodas LM, Campistol JM, Jeanpierre C, Alam S, Casale P, Wong CS, Lin F, Miranda DM, Oliveira EA, Simões-E-Silva AC, Barasch JM, Levy B, Wu N, Hildebrandt F, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Zhang F, Hakonarson H, Papaioannou VE, Mendelsohn CL, Gharavi AG, Sanna-Cherchi S. Verbitsky M, et al. Among authors: tkaczyk m. Nat Genet. 2019 Jan;51(1):117-127. doi: 10.1038/s41588-018-0281-y. Epub 2018 Dec 21. Nat Genet. 2019. PMID: 30578417 Free PMC article.
Markers of bone metabolism are affected by renal function and growth hormone therapy in children with chronic kidney disease.
Doyon A, Fischer DC, Bayazit AK, Canpolat N, Duzova A, Sözeri B, Bacchetta J, Balat A, Büscher A, Candan C, Cakar N, Donmez O, Dusek J, Heckel M, Klaus G, Mir S, Özcelik G, Sever L, Shroff R, Vidal E, Wühl E, Gondan M, Melk A, Querfeld U, Haffner D, Schaefer F; 4C Study Consortium. Doyon A, et al. PLoS One. 2015 Feb 6;10(2):e0113482. doi: 10.1371/journal.pone.0113482. eCollection 2015. PLoS One. 2015. PMID: 25659076 Free PMC article. Clinical Trial.
Hypertension in dialysed children: the prevalence and therapeutic approach in Poland--a nationwide survey.
Tkaczyk M, Nowicki M, Bałasz-Chmielewska I, Boguszewska-Baçzkowska H, Drozdz D, Kołłataj B, Jarmoliński T, Jobs K, Kiliś-Pstrusińska K, Leszczyńska B, Makulska I, Runowski D, Stankiewicz R, Szczepańska M, Wierciński R, Grenda R, Kanik A, Pietrzyk JA, Roszkowska-Blaim M, Szprynger K, Zachwieja J, Zajaczkowska MM, Zoch-Zwierz W, Zwolińska D, Zurowska A. Tkaczyk M, et al. Nephrol Dial Transplant. 2006 Mar;21(3):736-42. doi: 10.1093/ndt/gfi280. Epub 2005 Nov 22. Nephrol Dial Transplant. 2006. PMID: 16303782
Anaemia treatment in chronically dialysed children: a multicentre nationwide observational study.
Jander A, Wierciński R, Bałasz-Chmielewska I, Miklaszewska M, Zachwieja K, Borzecka H, Zachwieja J, Olszak-Szot I, Kubicki D, Ziółkowska H, Rubik J, Szczepańska M, Runowski D, Fendler W, Tkaczyk M. Jander A, et al. Among authors: tkaczyk m. Scand J Urol Nephrol. 2012 Oct;46(5):375-80. doi: 10.3109/00365599.2012.685492. Epub 2012 May 16. Scand J Urol Nephrol. 2012. PMID: 22587334
Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population.
Lipska BS, Balasz-Chmielewska I, Morzuch L, Wasielewski K, Vetter D, Borzecka H, Drozdz D, Firszt-Adamczyk A, Gacka E, Jarmolinski T, Ksiazek J, Kuzma-Mroczkowska E, Litwin M, Medynska A, Silska M, Szczepanska M, Tkaczyk M, Wasilewska A, Schaefer F, Zurowska A, Limon J. Lipska BS, et al. Among authors: tkaczyk m. J Appl Genet. 2013 Aug;54(3):327-33. doi: 10.1007/s13353-013-0147-z. Epub 2013 May 5. J Appl Genet. 2013. PMID: 23645318 Free PMC article.
Anxiety in children and adolescents with chronic kidney disease--multicenter national study results.
Kiliś-Pstrusińska K, Medyńska A, Adamczak P, Bałasz-Chmielewska I, Grenda R, Kluska-Jóźwiak A, Leszczyńska B, Olszak-Szot I, Miklaszewska M, Szczepańska M, Tkaczyk M, Wasilewska A, Zachwieja K, Zajączkowska M, Ziółkowska H, Zagożdżon I, Zwolińska D. Kiliś-Pstrusińska K, et al. Among authors: tkaczyk m. Kidney Blood Press Res. 2013;37(6):579-87. doi: 10.1159/000355738. Epub 2013 Dec 3. Kidney Blood Press Res. 2013. PMID: 24356548 Free article.
Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations.
Sikora P, Zaniew M, Haisch L, Pulcer B, Szczepańska M, Moczulska A, Rogowska-Kalisz A, Bieniaś B, Tkaczyk M, Ostalska-Nowicka D, Zachwieja K, Hyla-Klekot L, Schlingmann KP, Konrad M. Sikora P, et al. Among authors: tkaczyk m. Nephrol Dial Transplant. 2015 Apr;30(4):636-44. doi: 10.1093/ndt/gfu374. Epub 2014 Dec 3. Nephrol Dial Transplant. 2015. PMID: 25477417
145 results