Medicine and Dentistry
Phenylketonuria
100%
Phenylalanine
71%
Supplementation
38%
Amino Acid
38%
Diet Restriction
25%
Diet Therapy
11%
Systematic Review
8%
Gut Microbiome
8%
Disks Large Homolog 4
8%
Cell Body
8%
Type I Tyrosinemia
8%
Oxidative Stress
8%
Tetrahydrobiopterin
8%
Brain Monoamine
6%
Keyphrases
Phenylketonuria
66%
Phenylalanine
40%
Large Neutral Amino Acids
26%
Phenylalanine Restriction
18%
Amino Acid Supplementation
16%
Monoamines
10%
Repurposing Approaches
9%
Tyrosinemia Type 1
8%
Patient Evidence
8%
Synergistic Mechanism
8%
Dopamine Deficiency
8%
Brain Function
8%
Aminoacidopathies
8%
Specific nutrients
8%
Dietary Intervention
8%
Intellectual Disability
8%
Tetrahydrobiopterin
8%
Neurocognitive Deficits
8%
Pahenu2 Mice
8%
Blood Biochemistry
8%
Brain Biochemistry
8%
Blood Phenylalanine
7%
Brain Monoamines
6%
Biochemistry, Genetics and Molecular Biology
Phenylketonuria
50%
Mouse
34%
Amino Acids
25%
Phenylalanine
20%
Biochemistry
17%
Neurotransmitter
12%
Mouse Model
10%
Genetic Background
8%
Tetrahydrobiopterin
8%
Phenylalanine
8%
Intellectual Disability
8%
Fibroblast
5%
Fumarylacetoacetate Hydrolase
5%
