Low bone mineralization in phenylketonuria may be due to undiagnosed metabolic acidosis
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference69 articles.
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3. Long-term dietary intervention with low Phe and/or a specific nutrient combination improve certain aspects of brain functioning in phenylketonuria (PKU);Bruinenberg;PLoS One,2019
4. White and gray matter brain development in children and young adults with phenylketonuria;Hawks;NeuroImage Clin.,2019
5. Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria;Longo;Genet. Med.,2019
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