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Germline Mutation in KIF1Bβ Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma.
De Filpo G, Contini E, Serio V, Valeri A, Chetta M, Guasti D, Bani D, Mannelli M, Rapizzi E, Luconi M, Maggi M, Ercolino T, Canu L. De Filpo G, et al. Among authors: canu l. Int J Endocrinol. 2020 May 30;2020:3671396. doi: 10.1155/2020/3671396. eCollection 2020. Int J Endocrinol. 2020. PMID: 32565791 Free PMC article.
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: canu l. 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
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. 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
Novel somatic mutations in the catalytic subunit of the protein kinase A as a cause of adrenal Cushing's syndrome: a European multicentric study.
Di Dalmazi G, Kisker C, Calebiro D, Mannelli M, Canu L, Arnaldi G, Quinkler M, Rayes N, Tabarin A, Laure Jullié M, Mantero F, Rubin B, Waldmann J, Bartsch DK, Pasquali R, Lohse M, Allolio B, Fassnacht M, Beuschlein F, Reincke M. Di Dalmazi G, et al. Among authors: canu l. J Clin Endocrinol Metab. 2014 Oct;99(10):E2093-100. doi: 10.1210/jc.2014-2152. Epub 2014 Jul 24. J Clin Endocrinol Metab. 2014. PMID: 25057884
117 results