Zobrazeno 1 - 3
of 3
pro vyhledávání: '"von Hippel-Lindau Disease/complications"'
Autor:
M. A. M. Feldberg, F. J. Hes
Publikováno v:
European Radiology. 9:598-610
Von Hippel-Lindau disease (VHL) is a hereditary syndrome characterized by a predisposition for bilateral and multicentric retinal angiomas, hemangioblastomas in the central nervous system (CNS), renal cell carcinomas, pheochromocytomas, islet cell tu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7230abf0f0d2dcdc37bb4ffe1b5aceb9
https://doi.org/10.1007/s003300050717
https://doi.org/10.1007/s003300050717
Autor:
Hes, F J, Slootweg, P J, van Vroonhoven, T J, Hené, R J, Feldberg, M A, Zewald, R A, Ploos van Amstel, J K, Höppener, J W, Pearson, P L, Lips, C J
BACKGROUND: An evaluation of nephron-sparing surgery (NSS) or radical nephrectomy (RN) for treating renal cell carcinoma (RCC) in patients with von Hippel-Lindau disease (VHL) was carried out. METHODS: Between 1976 and 1997, 10 patients with RCC from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::43ca75661123cf7b1161eceb25016001
https://biblio.vub.ac.be/vubir/management-of-renal-cell-carcinoma-in-von-hippellindau-disease(67bb19a1-8c16-421d-80fd-071f577fc32f).html
https://biblio.vub.ac.be/vubir/management-of-renal-cell-carcinoma-in-von-hippellindau-disease(67bb19a1-8c16-421d-80fd-071f577fc32f).html
