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Ear and Hearing|October 6, 2012
Children with phenylketonuria treated early: basic audiological and electrophysiological evaluationPatrícia Cotta Mancini, John D Durrant, Ana Lúcia Pimenta Starling, et al.Jornal De Pediatria|March 30, 2012
Relationships between phenylalanine levels, intelligence and socioeconomic status of patients with phenylketonuriaIsabel Pimenta Spínola Castro, Juliana Martins Borges, Heloísa Alves Chagas, et al.Molecular Genetics and Metabolism Reports|May 20, 2020
Body fat percentage in adolescents with phenylketonuria and associated factorsGiovanna Caliman Camatta, Viviane de Cássia Kanufre, Michelle Rosa Andrade Alves, et al.Genetics and Molecular Research : GMR|June 7, 2006
Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, BrazilLuciana Lara dos Santos, Myrian de Castro Magalhães, Adriana de Oliveira Reis, et al.Journal of Medical Screening|December 5, 2019
Frequency of biotinidase gene variants and incidence of biotinidase deficiency in the Newborn Screening Program in Minas Gerais, BrazilNara de Oliveira Carvalho, José Nélio Januário, Gilsimary Lessa Pereira Felix, et al.Jornal De Pediatria|August 13, 2017
BH4 deficiency identified in a neonatal screening program for hyperphenylalaninemiaCezar Antonio Abreu de Souza, Michelle Rosa Andrade Alves, Rosangelis Del Lama Soares, et al.Jornal De Pediatria|October 15, 2022
Nonalcoholic fatty liver disease in adolescents with phenylketonuriaAdriana Márcia Silveira, Poliane Lopes Lima, Michelle Rosa Andrade Alves, et al.Jornal De Pediatria|June 18, 2021
Overweight/obesity in adolescents with phenylketonuria: protective and predisposing factorsAdriana Márcia Silveira, Poliane Lopes Lima, Michelle Rosa Andrade Alves, et al.Pageof 1