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Page 1
Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility.
Toledo RA, Hatakana R, Lourenço DM Jr, Lindsey SC, Camacho CP, Almeida M, Lima JV Jr, Sekiya T, Garralda E, Naslavsky MS, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJ, Lebrao ML, Duarte YA, Blangero J, Zatz M, Cerutti JM, Maciel RM, Toledo SP. Toledo RA, et al. Among authors: toledo sp. Endocr Relat Cancer. 2015 Feb;22(1):65-76. doi: 10.1530/ERC-14-0491. Epub 2014 Nov 25. Endocr Relat Cancer. 2015. PMID: 25425582 Free PMC article.
Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1.
Toledo RA, Lourenço DM Jr, Coutinho FL, Quedas E, Mackowiack I, Machado MC, Montenegro F, Cunha-Neto MB, Liberman B, Pereira MA, Correa PH, Toledo SP. Toledo RA, et al. Among authors: toledo sp. Clin Endocrinol (Oxf). 2007 Sep;67(3):377-84. doi: 10.1111/j.1365-2265.2007.02895.x. Epub 2007 Jun 6. Clin Endocrinol (Oxf). 2007. PMID: 17555499
Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile.
Lourenço DM Jr, Toledo RA, Mackowiak II, Coutinho FL, Cavalcanti MG, Correia-Deur JE, Montenegro F, Siqueira SA, Margarido LC, Machado MC, Toledo SP. Lourenço DM Jr, et al. Among authors: toledo ra, toledo sp. Eur J Endocrinol. 2008 Sep;159(3):259-74. doi: 10.1530/EJE-08-0153. Epub 2008 Jun 4. Eur J Endocrinol. 2008. PMID: 18524795
Sporadic medullary thyroid carcinoma: clinical data from a university hospital.
Correia-Deur JE, Toledo RA, Imazawa AT, Lourenço DM Jr, Ezabella MC, Tavares MR, Toledo SP. Correia-Deur JE, et al. Among authors: toledo ra, toledo sp. Clinics (Sao Paulo). 2009 May;64(5):379-86. doi: 10.1590/s1807-59322009000500002. Clinics (Sao Paulo). 2009. PMID: 19488601 Free PMC article.
Hypercalcitoninemia is not pathognomonic of medullary thyroid carcinoma.
Toledo SP, Lourenço DM Jr, Santos MA, Tavares MR, Toledo RA, Correia-Deur JE. Toledo SP, et al. Among authors: toledo ra. Clinics (Sao Paulo). 2009;64(7):699-706. doi: 10.1590/S1807-59322009000700015. Clinics (Sao Paulo). 2009. PMID: 19606248 Free PMC article. Review.
High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene.
Toledo RA, Wagner SM, Coutinho FL, Lourenço DM Jr, Azevedo JA, Longuini VC, Reis MT, Siqueira SA, Lucon AM, Tavares MR, Fragoso MC, Pereira AA, Dahia PL, Mulligan LM, Toledo SP. Toledo RA, et al. Among authors: toledo sp. J Clin Endocrinol Metab. 2010 Mar;95(3):1318-27. doi: 10.1210/jc.2009-1355. Epub 2010 Jan 15. J Clin Endocrinol Metab. 2010. PMID: 20080836
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.
Qin Y, Yao L, King EE, Buddavarapu K, Lenci RE, Chocron ES, Lechleiter JD, Sass M, Aronin N, Schiavi F, Boaretto F, Opocher G, Toledo RA, Toledo SP, Stiles C, Aguiar RC, Dahia PL. Qin Y, et al. Among authors: toledo ra, toledo sp. Nat Genet. 2010 Mar;42(3):229-33. doi: 10.1038/ng.533. Epub 2010 Feb 14. Nat Genet. 2010. PMID: 20154675 Free PMC article.
116 results