Last Updated: 09/26/2026
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Found 5 publications
Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 14, 2018
Pegvaliase for the treatment of phenylketonuria: A pivotal, double-blind randomized discontinuation Phase 3 clinical trial.
Journal: Molecular genetics and metabolism
Published: January 14, 2018
Refeeding syndrome in a young woman with argininosuccinate lyase deficiency.
Journal: Molecular genetics and metabolism reports
Published: March 04, 2016
Intermediate MCAD Deficiency Associated with a Novel Mutation of the ACADM Gene: c.1052C>T.
Journal: Case reports in genetics
Published: August 13, 2015
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.
Journal: Orphanet journal of rare diseases
Published: April 08, 2015
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Last Updated: 09/26/2026