Alicia De La Parra
Santiago, RM, Chile
Last Updated: 09/26/2026
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Found 8 publications
Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway.
Journal: Journal of inherited metabolic disease
Published: March 04, 2022
Maple syrup urine disease: Characteristics of diagnosis and treatment in 45 patients in Chile.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: November 22, 2020
Case report: Maternal tyrosinemia type 1a under NTBC treatment with tyrosine- and phenylalanine restricted diet in Chile.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: October 10, 2020
First-year metabolic control guidelines and their impact on future metabolic control and neurocognitive functioning in children with PKU.
Journal: Molecular genetics and metabolism reports
Published: July 28, 2017
Treatment adherence during childhood in individuals with phenylketonuria: Early signs of treatment discontinuation.
Journal: Molecular genetics and metabolism reports
Published: November 25, 2016
Long-term cognitive functioning in individuals with tyrosinemia type 1 treated with nitisinone and protein-restricted diet.
Journal: Molecular genetics and metabolism reports
Published: November 04, 2016
Cognitive functioning in mild hyperphenylalaninemia.
Journal: Molecular genetics and metabolism reports
Published: October 15, 2015
Propionic acidemia and optic neuropathy: a report of two cases.
Journal: JIMD reports
Published: February 26, 2013
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Last Updated: 09/26/2026