hippuric acid has been researched along with Phenylketonurias in 2 studies
hippuric acid: RN given refers to parent cpd; structure in Merck Index, 9th ed, #4591
N-benzoylglycine : An N-acylglycine in which the acyl group is specified as benzoyl.
Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hoskins, JA | 2 |
| Holliday, SB | 1 |
| Greenway, AM | 1 |
| Gray, J | 1 |
2 other studies available for hippuric acid and Phenylketonurias
| Article | Year |
|---|---|
The metabolism of cinnamic acid by healthy and phenylketonuric adults: a kinetic study.
Topics: Adult; Cinnamates; Female; Gas Chromatography-Mass Spectrometry; Hippurates; Humans; Kinetics; Male; | 1984 |
Phenylalanine ammonia lyase in the management of phenylketonuria: the relationship between ingested cinnamate and urinary hippurate in humans.
Topics: Adolescent; Adult; Ammonia-Lyases; Cinnamates; Diet; Dietary Proteins; Hippurates; Humans; Middle Ag | 1982 |