Medicine & Life Sciences
3-Hydroxyacyl-CoA Dehydrogenase
18%
4-phenylbutyric acid
8%
Acyl-CoA Dehydrogenase
7%
acylcarnitine
7%
Ammonia
13%
Argininosuccinate Lyase
6%
Argininosuccinic Aciduria
5%
Biomarkers
5%
Brain
5%
Carnitine
5%
Child
9%
Diet
10%
Dietary Proteins
6%
Enzymes
5%
Exons
6%
Fatty Acids
14%
fumarylacetoacetase
12%
Gene Editing
5%
Genes
8%
Genetic Therapy
18%
Glutamine
6%
glycerol phenylbutyrate
29%
Hepatocytes
12%
Inborn Errors Metabolism
12%
Inborn Urea Cycle Disorder
55%
Liver
16%
Methylmalonic acidemia
8%
Mutation
10%
Neonatal Screening
10%
Nutrition Therapy
5%
pegvaliase
43%
Phase III Clinical Trials
8%
Phenotype
6%
phenylacetic acid
8%
phenylacetylglutamine
8%
Phenylalanine
44%
Phenylalanine Ammonia-Lyase
9%
Phenylalanine Hydroxylase
30%
Phenylketonurias
100%
Safety
6%
sapropterin
18%
Sarcosinemia
7%
Swine
5%
Therapeutics
12%
Trifunctional Protein Deficiency With Myopathy And Neuropathy
28%
Triglycerides
6%
triheptanoin
7%
Tyrosine
5%
VLCAD deficiency
6%
Chemical Compounds
3-Hydroxyacyl-CoA
15%
Acyl-CoA
11%
Ammonia
6%
Disorder
22%
Long-Chain Fatty Acid
5%
Metabolic
5%
Mutation
6%
Pharmacological Metabolism
6%
Phenylacetic Acid
6%
Phenylalanine
36%
Plasma
6%
Protein
7%
Safety
6%
Sapropterin
14%
Sapropterin Dihydrochloride
9%
Sodium Phenylbutyrate
7%
Urea
14%