3-hydroxymandelic acid has been researched along with Phenylketonurias in 1 studies
*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). [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (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 |
|---|---|
| Greenway, AM; Hoskins, JA | 1 |
1 other study(ies) available for 3-hydroxymandelic acid and Phenylketonurias
| Article | Year |
|---|---|
The metabolism of L-m-tyrosine: the use of a putative precursor to investigate the increased production of m-hydroxymandelic acid in phenylketonuria.
Topics: 2-Hydroxyphenethylamine; 3,4-Dihydroxyphenylacetic Acid; Adult; Female; Humans; Hydroxylation; Kinetics; Male; Mandelic Acids; Octopamine; Phenylacetates; Phenylketonurias; Tyrosine | 1983 |