Centralization of care for rare genetic syndromes associated with cancer: improving outcomes and advancing research on VHL disease
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Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41585-024-00874-y.pdf
Reference29 articles.
1. Orphanet An online rare disease and orphan drug data base. © INSERM 1999. Available on http://www.orpha.net. (2023). Accessed on 27 December 2023.
2. Ferreira, C. R. The burden of rare diseases. Am. J. Med. Genet. A 179, 885–892 (2019).
3. 100,000 Genomes Project Pilot Investigators. et al. 100,000 genomes pilot on rare-disease diagnosis in health care — preliminary report. N. Engl. J. Med. 385, 1868–1880 (2021).
4. Ball, M. W. et al. Growth rates of genetically defined renal tumors: implications for active surveillance and intervention. J. Clin. Oncol. 38, 1146–1153 (2020).
5. Ljungberg, B. et al. European Association of Urology guidelines on renal cell carcinoma: the 2022 update. Eur. Urol. 82, 399–410 (2022).
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