Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mc Kiernan, PJ"'
Autor:
Saland, JM, Ruggenenti, P, Remuzzi, G, Bekassy, Z, Bensman, A, Bresin, E, Colledan, M, Camilla, R, Coppo, R, Cruzado-Garrit, JM, Daina, E, Fremeaux-Bacchi, V, Goodship, TJ, Gridelli, B, Hugo, C, Karpman, D, Jalanko, H, Loirat, C, Hijosa, MM, Mc Kiernan, PJ, Noris, M, De Cordoba, SR, Rota, G, Sanchez-Corral, P, Skerka, C, Tartufari, A, Zipfel, PF
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
10 páginas, 8 tablas -- PAGS nros. 940-949
Atypical hemolytic uremic syndrome is often associated with mutations in genes encoding complement regulatory proteins and secondary disorders of complement regulation. Progression to kidney failure an
Atypical hemolytic uremic syndrome is often associated with mutations in genes encoding complement regulatory proteins and secondary disorders of complement regulation. Progression to kidney failure an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37762c5b94e8b25ad911d5aa78f7cf28
http://hdl.handle.net/10281/365467
http://hdl.handle.net/10281/365467
Autor:
Mc Kiernan PJ; Division of Gastroenterology/Hepatology/Nutrition Children's Hospital of Pittsburgh of UPMC, Pittsburgh Liver Research Centre, University of Pitttsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA. patrick.mckiernan@chp.edu.
Publikováno v:
Journal of inherited metabolic disease [J Inherit Metab Dis] 2017 Jul; Vol. 40 (4), pp. 491-495. Date of Electronic Publication: 2017 Feb 06.
