Medicine & Life Sciences
Phenylketonurias
100%
Inborn Urea Cycle Disorder
54%
Phenylalanine
43%
pegvaliase
42%
Trifunctional Protein Deficiency With Myopathy And Neuropathy
31%
Phenylalanine Hydroxylase
29%
glycerol phenylbutyrate
28%
3-Hydroxyacyl-CoA Dehydrogenase
18%
Genetic Therapy
18%
sapropterin
17%
Liver
16%
Fatty Acids
14%
Ammonia
13%
Hepatocytes
13%
Inborn Errors Metabolism
12%
Therapeutics
12%
Neonatal Screening
11%
fumarylacetoacetase
11%
Mutation
10%
Diet
10%
Phenylalanine Ammonia-Lyase
9%
Child
9%
Phase III Clinical Trials
8%
4-phenylbutyric acid
8%
phenylacetylglutamine
8%
Methylmalonic acidemia
8%
Genes
7%
phenylacetic acid
7%
Phenotype
7%
Sarcosinemia
7%
Acyl-CoA Dehydrogenase
7%
acylcarnitine
7%
triheptanoin
6%
Glutamine
6%
Oxidoreductases
6%
Safety
6%
Exons
6%
Carnitine
6%
VLCAD deficiency
6%
Argininosuccinate Lyase
5%
Dietary Proteins
5%
Triglycerides
5%
Gene Editing
5%
Swine
5%
Biomarkers
5%
Tyrosine
5%
Brain
5%
Enzymes
5%
Nutrition Therapy
5%
Chemical Compounds
Phenylalanine
35%
Disorder
21%
3-Hydroxyacyl-CoA
15%
Sapropterin
14%
Urea
13%
Acyl-CoA
10%
Sapropterin Dihydrochloride
8%
Protein
7%
Sodium Phenylbutyrate
7%
Plasma
6%
Mutation
6%
Ammonia
6%
Safety
6%
Pharmacological Metabolism
6%
Phenylacetic Acid
5%
Long-Chain Fatty Acid
5%
Metabolic
5%