Aspectos clínicos e demográficos da fenilcetonúria no Estado da Bahia

by Amorim,Tatiana, Boa-Sorte,Ney, Leite,Maria Efigênia Q, Acosta,Angelina Xavier
Published 2011

Hemoglobin A2 values in sickle cell disease patients quantified by high performance liquid chromatography and the influence of alpha thalassemia

by Fonseca,Silvana Fahel da, Amorim,Tatiana, Purificação,Antônio, Gonçalves,Marilda, Boa-Sorte,Ney
Published 2015

Dried blood spot testing for the antenatal screening of HTLV, HIV, syphilis, toxoplasmosis and hepatitis B and C: prevalence, accuracy and operational aspects

by Boa-Sorte,Ney, Purificação,Antônio, Amorim,Tatiana, Assunção,Lorena, Reis,Alan, Galvão-Castro,Bernardo
Published 2014

METABOLIC CONTROL AND BODY COMPOSITION OF CHILDREN AND ADOLESCENTS WITH PHENYLKETONURIA

by Nogueira,Zeni Drubi, Boa-Sorte,Ney, Leite,Maria Efigênia de Queiroz, Toralles,Maria Betânia Pereira, Amorim,Tatiana
Published 2021

Breastfeeding and the anthropometric profile of children with sickle cell anemia receiving follow-up in a newborn screening reference service

by Nogueira,Zeni Drubi, Boa-Sorte,Ney, Leite,Maria Efigênia de Queiroz, Kiya,Márcia Miyuki, Amorim,Tatiana, Fonseca,Silvana Fahel da
Published 2015

Five-year performance analysis of a cystic fibrosis newborn screening program in northeastern Brazil

by Godoy,Carolina, Paixão,Danielle C., Boa-Sorte,Ney C.A., Amorim,Tatiana, da Silva Filho,Luiz Vicente R.F., Souza Filho,Edna Lúcia
Published 2023

Aspectos clínicos da fenilcetonúria em serviço de referência em triagem neonatal da Bahia

by Amorim,Tatiana, Gatto,Sara P.P., Boa-Sorte,Ney, Leite,Maria Efigênia Q., Fontes,Maria Inês M. M., Barretto,Junaura, Acosta,Angelina X.
Published 2005

The c.63A>G polymorphism in the NKX2.5 gene is associated with thyroid hypoplasia in children with thyroid dysgenesis

by Cerqueira,Taise Lima de Oliveira, Ramos,Yanne, Strappa,Giorgia, Martin,Daniel San, Jesus,Mariana, Gonzaga,Jailciele, Ferreira,Paulo, Costa,Anabel, Fernandes,Vladimir, Amorim,Tatiana, Ladeia,Ana Marice, Ramos,Helton
Published 2015

Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis

by Cerqueira,Taíse Lima de Oliveira, Ramos,Yanne Rocha, Strappa,Giorgia Bruna, Jesus,Mariana Souza de, Santos,Jailciele Gonzaga, Sousa,Camila, Carvalho,Gildásio, Fernandes,Vladimir, Boa-Sorte,Ney, Amorim,Tatiana, Silva,Thiago Magalhães, Ladeia,Ana Marice Teixeira, Acosta,Angelina Xavier, Ramos,Helton Estrela
Published 2018

Population medical genetics: translating science to the community

by Giugliani,Roberto, Bender,Fernanda, Couto,Rowena, Bochernitsan,Aline, Brusius-Facchin,Ana Carolina, Burin,Maira, Amorim,Tatiana, Acosta,Angelina Xavier, Purificação,Antônio, Leistner-Segal,Sandra, Saraiva-Pereira,Maria Luiza, Jardim,Laura Bannach, Matte,Ursula, Riegel,Mariluce, Cardoso-dos-Santos,Augusto César, Rodrigues,Graziella, Oliveira,Marcelo Zagonel de, Tagliani-Ribeiro,Alice, Heck,Selia, Dresch,Vanusa, Schuler-Faccini,Lavínia, Kubaski,Francyne
Published 2019