Outcomes in 14 live births resulting from Pegvaliase-treated pregnancies in PKU-affected females-Reference-Cited by-同舟云学术

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Outcomes in 14 live births resulting from Pegvaliase-treated pregnancies in PKU-affected females

Published:2024-03 Issue:3 Volume:141 Page:108152
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Bier Caide,Dickey Kaelin,Bibb Brittan,Crutcher Angela,Sponberg Rebecca,Chang Richard,Boyer Monica,Davis-Keppen Laura,Matthes Cindy,Tharp Michelle,Vice Danielle,Cooney Erin,Morand Megan,Ray Joseph,Lah Melissa,McNutt Markey,Andersson Hans C.

Publisher

Elsevier BV

Reference15 articles.

1. Phenylalanine hydroxylase deficiency: diagnosis and management guideline;Vockley;Genet. Med.,2014

2. Maternal phenylketonuria: a metabolic teratogen;Levy;Teratology.,1996

3. Effect of high maternal blood phenylalanine on offspring congenital anomalies and developmental outcome at ages 4 and 6 years: the importance of strict dietary control preconception and throughout pregnancy;Rouse;J. Pediatr.,2004

4. Efficacy of Sapropterin Dihydrochloride in increasing phenylalanine tolerance in children with phenylketonuria: a phase III Randomized, Double-Blind, Placebo-Controlled Study;Trefz;J. Pediatr.,2009

5. Long-term preservation of intellectual functioning in sapropterin-treated infants and young children with phenylketonuria: A seven-year analysis;Waisbren;Mol. Genet. Metab.,2021

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Phenylketonuria—Past, Present, and Future Directions;OBM Genetics;2024-08-16

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