A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases

por Vaz, Sara O., Pires, Renato, Pires, Luís M., Carreira, Isabel M., Anjos, Rui, Maciel, Paula, Mota-Vieira, Luisa
Publicado 2015

Quality of life and self-esteem in patients submitted to surgical treatment of skin carcinomas: long-term results()

por Maciel, Paula Curitiba, Veiga-Filho, Joel, de Carvalho, Marcelo Prado, Fonseca, Fernando Elias Martins, Ferreira, Lydia Masako, Veiga, Daniela Francescato
Publicado 2014

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

Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication

por Pires, Renato, Pires, Luís M, Vaz, Sara O, Maciel, Paula, Anjos, Rui, Moniz, Raquel, Branco, Claudia C, Cabral, Rita, Carreira, Isabel M, Mota-Vieira, Luisa
Publicado 2014

Early use of nitazoxanide in mild COVID-19 disease: randomised, placebo-controlled trial

por Rocco, Patricia R.M., Silva, Pedro L., Cruz, Fernanda F., Melo-Junior, Marco Antonio C., Tierno, Paulo F.G.M.M., Moura, Marcos A., De Oliveira, Luís Frederico G., Lima, Cristiano C., Dos Santos, Ezequiel A., Junior, Walter F., Fernandes, Ana Paula S.M., Franchini, Kleber G., Magri, Erick, de Moraes, Nara F., Gonçalves, José Mário J., Carbonieri, Melanie N., Dos Santos, Ivonise S., Paes, Natália F., Maciel, Paula V.M., Rocha, Raissa P., de Carvalho, Alex F., Alves, Pedro Augusto, Proença-Módena, José Luiz, Cordeiro, Artur T., Trivella, Daniela B.B., Marques, Rafael E., Luiz, Ronir R., Pelosi, Paolo, Lapa e Silva, Jose Roberto
Publicado 2021