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Pitfalls in genetic analysis of pheochromocytomas/paragangliomas-case report.
Canu L, Rapizzi E, Zampetti B, Fucci R, Nesi G, Richter S, Qin N, Giachè V, Bergamini C, Parenti G, Valeri A, Ercolino T, Eisenhofer G, Mannelli M. Canu L, et al. Among authors: mannelli m. J Clin Endocrinol Metab. 2014 Jul;99(7):2321-6. doi: 10.1210/jc.2013-4453. Epub 2014 Apr 23. J Clin Endocrinol Metab. 2014. PMID: 24758185
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
Piccini V, Rapizzi E, Bacca A, Di Trapani G, Pulli R, Giachè V, Zampetti B, Lucci-Cordisco E, Canu L, Corsini E, Faggiano A, Deiana L, Carrara D, Tantardini V, Mariotti S, Ambrosio MR, Zatelli MC, Parenti G, Colao A, Pratesi C, Bernini G, Ercolino T, Mannelli M. Piccini V, et al. Among authors: mannelli m. Endocr Relat Cancer. 2012 Apr 10;19(2):149-55. doi: 10.1530/ERC-11-0369. Print 2012 Apr. Endocr Relat Cancer. 2012. PMID: 22241717
Pheochromocytomas and Paragangliomas as Causes of Endocrine Hypertension.
Canu L, Parenti G, De Filpo G, Mannelli M. Canu L, et al. Among authors: mannelli m. Front Endocrinol (Lausanne). 2019 Jun 4;10:333. doi: 10.3389/fendo.2019.00333. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31214117 Free PMC article. Review.
Uncommon clinical presentations of pheochromocytoma and paraganglioma in two different patients affected by two distinct novel VHL germline mutations.
Ercolino T, Becherini L, Valeri A, Maiello M, Gaglianò MS, Parenti G, Ramazzotti M, Piscitelli E, Simi L, Pinzani P, Nesi G, Degl'Innocenti D, Console N, Bergamini C, Mannelli M. Ercolino T, et al. Among authors: mannelli m. Clin Endocrinol (Oxf). 2008 May;68(5):762-8. doi: 10.1111/j.1365-2265.2007.03131.x. Epub 2007 Nov 19. Clin Endocrinol (Oxf). 2008. PMID: 18031321
649 results