Medicine & Life Sciences
Phenylketonurias
100%
Inborn Urea Cycle Disorder
53%
Phenylalanine
43%
pegvaliase
40%
Phenylalanine Hydroxylase
31%
glycerol phenylbutyrate
30%
Trifunctional Protein Deficiency With Myopathy And Neuropathy
29%
3-Hydroxyacyl-CoA Dehydrogenase
19%
Genetic Therapy
19%
Liver
17%
sapropterin
15%
Fatty Acids
15%
Ammonia
14%
Inborn Errors Metabolism
12%
fumarylacetoacetase
12%
Hepatocytes
12%
Therapeutics
12%
Mutation
10%
Diet
10%
Neonatal Screening
10%
Phenylalanine Ammonia-Lyase
10%
Child
9%
Phase III Clinical Trials
8%
4-phenylbutyric acid
8%
phenylacetylglutamine
8%
Methylmalonic acidemia
8%
Genes
8%
phenylacetic acid
8%
Sarcosinemia
7%
Acyl-CoA Dehydrogenase
7%
acylcarnitine
7%
triheptanoin
7%
Glutamine
7%
Phenotype
6%
Safety
6%
Exons
6%
VLCAD deficiency
6%
Argininosuccinate Lyase
6%
Dietary Proteins
6%
Triglycerides
6%
Carnitine
6%
Gene Editing
5%
Swine
5%
Biomarkers
5%
Tyrosine
5%
Brain
5%
Argininosuccinic Aciduria
5%
Vitamin B 12
5%
Oxidoreductases
5%
Chemical Compounds
Phenylalanine
35%
Disorder
22%
3-Hydroxyacyl-CoA
15%
Urea
14%
Acyl-CoA
11%
Sapropterin
10%
Sapropterin Dihydrochloride
9%
Protein
8%
Sodium Phenylbutyrate
8%
Plasma
7%
Mutation
6%
Ammonia
6%
Pharmacological Metabolism
6%
Safety
6%
Phenylacetic Acid
6%
Long-Chain Fatty Acid
6%
Metabolic
5%