The Clinical and Molecular Features in the VHL Renal Cancers; Close or Distant Relatives with Sporadic Clear Cell Renal Cell Carcinoma?

SIMPLE SUMMARY: VHL syndrome is an autosomal dominant hereditary cancer syndrome and one of the leading causes of death is ccRCC. Current target therapies may lead to stable disease or partial remission, as best response and scant evidence supports the therapeutic decision-making in metastatic ccRCC...

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Detalles Bibliográficos
Autores principales: Cinque, Alessandra, Minnei, Roberto, Floris, Matteo, Trevisani, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657498/
https://www.ncbi.nlm.nih.gov/pubmed/36358771
http://dx.doi.org/10.3390/cancers14215352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657498/
https://www.ncbi.nlm.nih.gov/pubmed/36358771
http://dx.doi.org/10.3390/cancers14215352

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