Schuhmacher P

No ORCID on file · 1 paper in corpus · active 2019
2019
Orphanet journal of rare diseases ·doi:10.1186/s13023-019-1206-2

BackgroundVon Hippel-Lindau (VHL) disease is a multi-systemic hereditary disease associated with several benign and malignant tumor entities, including clear cell renal cell carcinoma (ccRCC). Since ccRCCs grow slowly, nephron sparing surge…