Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil

por Toledo, Rodrigo A., Sekiya, Tomoko, Longuini, Viviane C., L. Coutinho, Flavia, Lourenço, Delmar M., Toledo, Sergio P. A.
Publicado 2012

RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family

por Quedas, Elisangela P. S., Longuini, Viviane C., Sekiya, Tomoko, Coutinho, Flavia L., Toledo, Sergio P. A., Tannuri, Uenis, Toledo, Rodrigo A.
Publicado 2012

Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility

por Toledo, Rodrigo A, Hatakana, Roxanne, Lourenço, Delmar M, Lindsey, Susan C, Camacho, Cleber P, Almeida, Marcio, Lima, José V, Sekiya, Tomoko, Garralda, Elena, Naslavsky, Michel S, Yamamoto, Guilherme L, Lazar, Monize, Meirelles, Osorio, Sobreira, Tiago J P, Lebrao, Maria Lucia, Duarte, Yeda A O, Blangero, John, Zatz, Mayana, Cerutti, Janete M, Maciel, Rui M B, Toledo, Sergio P A
Publicado 2015