Skip to main navigation
Skip to search
Skip to main content
UTMB Health Research Expert Profiles Home
Help & FAQ
Home
Experts
Departments
Equipment
Projects/Grants
Publications
Activities
Press/Media
Honors
Search by expertise, name or affiliation
Phenylketonuria: screening, treatment and maternal PKU
Reuben Matalon, Kimberlee Michals
Research output
:
Contribution to journal
›
Article
›
peer-review
22
Scopus citations
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Phenylketonuria: screening, treatment and maternal PKU'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
Phenylketonuria
100%
Maternal Phenylketonuria
100%
Phenylalanine Hydroxylase
27%
Blood Phenylalanine Level
27%
Hyperphenylalaninemia
27%
Blood Phenylalanine
18%
Baby Born
9%
During Pregnancy
9%
Molecular Biology
9%
Long-term Treatment
9%
Tyrosine
9%
Phenylalanine
9%
Poor School Performance
9%
Tetrahydrobiopterin
9%
Congenital Heart Defects
9%
Clinical Presentation
9%
Intellectual Disability
9%
Behavior Problems
9%
Tryptophan
9%
Classical Phenylketonuria
9%
Small-for-gestational Age
9%
Collaborative Study
9%
Appropriate Treatment
9%
Serious Complications
9%
Prenatal Diagnosis
9%
Normal Diet
9%
Microcephaly
9%
Newborn Period
9%
School Behavior
9%
Performance Problems
9%
Enzymatic Hydroxylation
9%
Subclassification
9%
Medicine and Dentistry
Phenylketonuria
100%
Phenylalanine
40%
Phenylalanine 4 Monooxygenase
20%
Hyperphenylalaninemia
20%
Disease
6%
Problem Behavior
6%
Small for Gestational Age
6%
Newborn Period
6%
Prenatal Diagnosis
6%
Microcephaly
6%
Congenital Heart Defect
6%
Tryptophan
6%
Tetrahydrobiopterin
6%
Hydroxylation
6%
Biochemistry, Genetics and Molecular Biology
Phenylketonuria
100%
Phenylalanine
40%
Phenylalanine Hydroxylase
20%
Molecular Biology
6%
Tyrosine
6%
Hydroxylation
6%
Tetrahydrobiopterin
6%
Problem Behavior
6%
Tryptophan
6%
Small for Date Infant
6%
Newborn Period
6%