Kristin E. Lindstrom
Medical Genetics | Pediatrics
1920 E Cambridge Ave Ste 304
Phoenix, AZ 85006
Phoenix, AZ 85006
Last Updated: 09/26/2026
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Found 44 publications
Management of pegvaliase-related skin concerns: best practice recommendations using a modified Delphi approach.
Journal: Molecular genetics and metabolism
Published: August 26, 2025
Long-term management strategies for pegvaliase use in phenylketonuria: Lessons learned from the phase-3 PRISM open-label extension study.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 20, 2024
Corrigendum to "Evaluating change in diet with pegvaliase treatment in adults with phenylketonuria: Analysis of phase 3 clinical trial data" [Molecular Genetics and Metabolism 141, Issue 3 (2024) 108122].
Journal: Molecular genetics and metabolism
Published: November 26, 2024
Pegvaliase for the treatment of phenylketonuria: Final results of a long-term phase 3 clinical trial program.
Journal: Molecular genetics and metabolism reports
Published: January 16, 2024
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Journal: American journal of human genetics
Published: December 08, 2023
Evaluating change in diet with pegvaliase treatment in adults with phenylketonuria: Analysis of phase 3 clinical trial data.
Journal: Molecular genetics and metabolism
Published: November 02, 2023
Best practice recommendations for the management of anxiety during the pegvaliase journey.
Journal: Molecular genetics and metabolism
Published: October 13, 2023
Efficacy and safety of sapropterin before and during pregnancy: Final analysis of the Kuvan® Adult Maternal Paediatric European Registry (KAMPER) maternal and Phenylketonuria Developmental Outcomes and Safety (PKUDOS) PKU-MOMs sub-registries.
Journal: Journal of inherited metabolic disease
Published: August 24, 2023
Long-term comparative effectiveness of pegvaliase versus medical nutrition therapy with and without sapropterin in adults with phenylketonuria.
Journal: Molecular genetics and metabolism
Published: August 13, 2023
Real-world treatment, dosing, and discontinuation patterns among patients treated with pegvaliase for phenylketonuria: Evidence from dispensing data.
Journal: Molecular genetics and metabolism reports
Published: September 15, 2022
Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features.
Journal: Genes
Published: December 21, 2021
A neonate with ornithine aminotransferase deficiency; insights on the hyperammonemia-associated biochemical phenotype of gyrate atrophy.
Journal: Molecular genetics and metabolism reports
Published: October 25, 2021
Last Updated: 09/26/2026