Consensus Linee Guida feocromocitoma/paraganglioma in pazienti portatori di varianti germinali a carico del gene SDHD
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s40619-024-01468-x.pdf
Reference10 articles.
1. Mannelli M, Canu L, Ercolino T et al. (2018) Diagnosis of endocrine disease: SDHx mutations: beyond pheochromocytomas and paragangliomas. Eur J Endocrinol 178:R11–R17
2. Burnichon N, Mazzella J-M, Drui D et al. (2017) Risk assessment of maternally inherited SDHD paraganglioma and phaeochromocytoma. J Med Genet 54:125–133
3. Taïeb D, Wanna GB, Ahmad M et al. (2023) Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants. Lancet Diabetes Endocrinol 11(5):345–361
4. Heesterman B, de Pont LM, Verbist BM et al. (2017) Age and tumor volume predict growth of carotid and vagal body paragangliomas. J Neurol Surg Part B Skull Base 78:497–505
5. Guss ZD, Batra S, Limb CJ et al. (2011) Radiosurgery of glomus jugulare tumors: a meta-analysis. Int J Radiat Oncol Biol Phys 81:e497–502
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