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 no Diabetol Metab Syndr (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 no Diabetol Metab Syndr (2015)

Amplification of the Insulin-Like Growth Factor 1 Receptor Gene Is a Rare Event in Adrenocortical Adenocarcinomas: Searching for Potential Mechanisms of Overexpression

Por Ribeiro, Tamaya Castro, Jorge, Alexander Augusto, Almeida, Madson Q., Mariani, Beatriz Marinho de Paula, Nishi, Mirian Yumi, Mendonca, Berenice Bilharinho, Fragoso, Maria Candida Barisson Villares, Latronico, Ana Claudia
Publicado em 2014

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 no Diabetol Metab Syndr (2015)

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 no Front Endocrinol (Lausanne) (2018)