Ana P. Starling
Belo Horizonte, MG, Brazil
Last Updated: 09/26/2026
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Found 9 publications
Nonalcoholic fatty liver disease in adolescents with phenylketonuria.
Journal: Jornal de pediatria
Published: March 06, 2022
Overweight/obesity in adolescents with phenylketonuria: protective and predisposing factors.
Journal: Jornal de pediatria
Published: September 30, 2020
Body fat percentage in adolescents with phenylketonuria and associated factors.
Journal: Molecular genetics and metabolism reports
Published: February 18, 2020
Frequency of biotinidase gene variants and incidence of biotinidase deficiency in the Newborn Screening Program in Minas Gerais, Brazil.
Journal: Journal of medical screening
Published: December 05, 2019
Novel mutations causing biotinidase deficiency in individuals identified by the newborn screening program in Minas Gerais, Brazil.
Journal: American journal of medical genetics. Part A
Published: January 02, 2019
BH4 deficiency identified in a neonatal screening program for hyperphenylalaninemia.
Journal: Jornal de pediatria
Published: October 24, 2016
Metabolic syndrome in children and adolescents with phenylketonuria.
Journal: Jornal de pediatria
Published: January 13, 2014
Children with phenylketonuria treated early: basic audiological and electrophysiological evaluation.
Children with phenylketonuria treated early: basic audiological and electrophysiological evaluation.
Journal: Ear and hearing
Published: October 06, 2012
Selenium intake and nutritional status of children with phenylketonuria in Minas Gerais, Brazil.
Journal: Jornal de pediatria
Published: November 22, 2011
Showing 1-9 of 9
Last Updated: 09/26/2026