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Transient hyperphenylalaninemia

A condition of not having consistently high levels of phenylalanine in the blood but of experiencing temporary hyperphenylalaninemia following… 
National Institutes of Health

Related topics

Related topics

1 relation
congenital deficiency

Papers overview

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2019
2019
Transient phenylketonuria in premature infants.
1996
1996
Newborn screening for certain treatable inborn errors of metabolism in Alexandria.
The study was conducted on two groups of newborn infants: Group A; a random sample of 3000 infants attending different Health… 
1993
1993
Progress in the study of biosynthesis and role of 7-substituted pterins: function of pterin-4a-carbinolamine dehydratase.
A new form of atypical phenylketonuria (PKU) was discovered in 1988. Characteristic for this transient hyperphenylalaninemia is… 
1992
1992
Phenylketonuria screening in Moscow using a microplate fluorometric method
Review
1969
Review
1969
Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.
The WIDESPREAD use of mass screening for blood phenylalanine among newborns has led to the recognition that in addition to… 
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