MODY screening: a new center for molecular genetic diagnosis in Brazil

por de Santana, Lucas Santos, Caetano, Lílian Araújo, Nery, Márcia, de Lima Jorge, Alexander Augusto, Bezerra, Milena Gurgel Teles
Publicado 2015

Next-generation sequencing in Brazilian MODY patients: a pilot study

por Caetano, Lílian Araújo, de Santana, Lucas Santos, Lerário, Antônio Marcondes, Nery, Márcia, de Lima Jorge, Alexander Augusto, Teles, Milena Gurgel
Publicado 2015

Detection of congenital generalized lipodystrophy mutations by next-generation sequencing: time for a new approach

por Riquetto, Aline Dantas Costa, de Santana, Lucas Santos, Caetano, Lílian Araújo, Lerário, Antônio Marcondes, Correia-Deur, Joya Emilie Menezes, Nery, Márcia, de Lima Jorge, Alexander Augusto, Teles, Milena Gurgel
Publicado 2015

Clinical and molecular update of a large cohort followed by the Brazilian MODY multicenter study group (BRASMODY)

por de Mello Almada Giuffrida, Fernando, Weinert, Leticia Schwerz, Moises, Regina C S, Calliari, Luis Eduardo, Manna, Thais Della, Caetano, Lilian Araujo, Teles, Milena G, Dotto, Renata Pires, Kunii, Ilda S, Silveiro, Sandra Pinho, da Silva, Magnus Regios Dias, Reis, André Fernandes
Publicado 2015

Searching for mutations in the HNF1B gene in a Brazilian cohort with renal cysts and hyperglycemia

por Dotto, Renata P., de Santana, Lucas Santos, Lindsey, Susan C., Caetano, Lilian Araújo, Franco, Luciana F., Moisés, Regina Célia M. S., Sa, João R., Nishiura, José Luiz, Teles, Milena Gurgel, Heilberg, Ita P., Dias-da-Silva, Magnus R., Giuffrida, Fernando M. A., Reis, André F.
Publicado 2019