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

OR15-04 Central Precocious Puberty without Central Nervous System Lesions: Is It Really Idiopathic?

por Canton, Ana Pinheiro-Machado, Brito, Vinicius Nahime, Montenegro, Luciana Ribeiro, Macedo, Delanie Bulcão, Bessa, Danielle de Souza, Silva, Marina Cunha, Seraphim, Carlos Eduardo, Piovesan, Maiara Ribeiro, Teles, Milena Gurgel, Silveira, Leticia Gontijo, Krepischi, Ana, Netchine, Irene, Mendonca, Berenice Bilharinho, Latronico, Ana Claudia
Publicado 2020

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

Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred

por Montenegro, Renan Magalhães, Costa-Riquetto, Aline Dantas, Fernandes, Virgínia Oliveira, Montenegro, Ana Paula Dias Rangel, de Santana, Lucas Santos, Jorge, Alexander Augusto de Lima, Karbage, Lia Beatriz de Azevedo Souza, Aguiar, Lindenberg Barbosa, Carvalho, Francisco Herlânio Costa, Teles, Milena Gurgel, d'Alva, Catarina Brasil
Publicado 2018