4-hydroxyphenylpyruvic acid has been researched along with Phenylketonurias in 2 studies
4-hydroxyphenylpyruvic acid: RN given refers to parent cpd
4-hydroxyphenylpyruvic acid : A 2-oxo monocarboxylic acid that is pyruvic acid in which one of the methyl hydrogens is substituted by a 4-hydroxyphenyl group.
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 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Mönch, E | 1 |
| Kneer, J | 1 |
| Jakobs, C | 1 |
| Arnold, M | 1 |
| Diehl, H | 1 |
| Batzler, U | 1 |
| Antoshechkin, AG | 1 |
| Zuyeva, LA | 1 |
| Maximova, LA | 1 |
2 other studies available for 4-hydroxyphenylpyruvic acid and Phenylketonurias
| Article | Year |
|---|---|
Examination of urine metabolites in the newborn period and during protein loading tests at 6 months of age--Part 1.
Topics: Creatinine; Dietary Proteins; Humans; Infant, Newborn; Phenylacetates; Phenylketonurias; Phenylpyruv | 1990 |
Excretion of phenylpyruvic, 4-hydroxyphenylpyruvic and indolyl-3-acetic acids by the skin fibroblasts from a phenylketonuric child.
Topics: Adult; Child, Preschool; Epidermis; Female; Fibroblasts; Humans; Indoleacetic Acids; Phenylketonuria | 1988 |