Successful long-term use of pioglitazone in Berardinelli–Seip lipodystrophy-associated diabetes

por Chaves, Carolina, Chaves, Mariana, Anselmo, João, César, Rui
Publicado 2021

SUN-447 Screening of Genetic Alterations in Patients with Giant Prolactinomas

por Chaves, Carolina, Chaves, Mariana, Serpa, Sara, Saramago, Ana, Leite, Valeriano, Cavaco, Branca, Anselmo, Joao D T S, Cesar, Rui
Publicado 2019

OR15-3 Extreme Phenotypic Variability of a Novel Mutation of MEN1 Gene in a Family with 14 Carriers across 3 Generations

por Chaves, Carolina, Chaves, Mariana, Pereira, Bernardo, Silva, David, Saramago, Ana, Leite, Valeriano, Cavaco, Branca, Anselmo, Joao D T S, Cesar, Rui
Publicado 2019

A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?

por Dias Pereira, Bernardo, Nunes da Silva, Tiago, Bernardo, Ana Teresa, César, Rui, Vara Luiz, Henrique, Pacak, Karel, Mota-Vieira, Luísa
Publicado 2018

Transient neonatal diabetes due to a missense mutation (E227K) in the gene encoding the ATP-sensitive potassium channel (KCNJ11)

por Martins, Luísa, Lourenço, Rita, Maia, Ana Lúcia, Maciel, Paula, Monteiro, Maria Isabel, Pacheco, Lucinda, Anselmo, João, César, Rui, Gomes, Maria Fernanda
Publicado 2015