Novel alternative tools for metastatic pheochromocytomas/paragangliomas prediction
Author:
Funder
CAMS Innovation Fund for Medical Sciences
National High Level Hospital Clinical Research Funding
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s40618-023-02239-5.pdf
Reference41 articles.
1. Beard CM, Sheps SG, Kurland LT, Carney JA, Lie JT (1983) Occurrence of pheochromocytoma in Rochester, Minnesota, 1950 through 1979. Mayo Clin Proc 58(12):802–804
2. Lenders JW, Duh QY, Eisenhofer G et al (2014) Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 99(6):1915–1942. https://doi.org/10.1210/jc.2014-1498
3. Lam AK (2017) Update on adrenal tumours in 2017 world health organization (WHO) of endocrine tumours. Endocr Pathol 28(3):213–227. https://doi.org/10.1007/s12022-017-9484-5
4. Eisenhofer G, Bornstein SR, Brouwers FM et al (2004) Malignant pheochromocytoma: current status and initiatives for future progress. Endocr Relat Cancer 11(3):423–436. https://doi.org/10.1677/erc.1.00829
5. Hescot S, Leboulleux S, Amar L et al (2013) One-year progression-free survival of therapy-naive patients with malignant pheochromocytoma and paraganglioma. J Clin Endocrinol Metab 98(10):4006–4012. https://doi.org/10.1210/jc.2013-1907
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