3-phenyllactic acid has been researched along with Phenylketonurias in 5 studies
3-phenyllactic acid: alpha-hydroxy analog of phenylalanine; RN given refers to cpd without isomeric designation
3-phenyllactic acid : A 2-hydroxy monocarboxylic acid that is lactic acid in which one of the methyl hydrogens is substituted by a phenyl 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 | 4 (80.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| WILLIAMS, CM | 1 |
| DORIN, GE | 1 |
| GREER, M | 1 |
| Sarkissian, CN | 1 |
| Scriver, CR | 1 |
| Mamer, OA | 1 |
| Spaapen, LJ | 1 |
| Ketting, D | 1 |
| Wadman, SK | 1 |
| Bruinvis, L | 1 |
| Duran, M | 1 |
| Hsiao, KJ | 1 |
| Hung, SH | 1 |
| Wu, SJ | 1 |
| Yeh, SF | 1 |
| Michals, K | 1 |
| Matalon, R | 1 |
5 other studies available for 3-phenyllactic acid and Phenylketonurias
| Article | Year |
|---|---|
DETERMINATION OF BETA-PHENYLLACTIC ACID BY GAS CHROMATOGRAPHY.
Topics: Chromatography; Chromatography, Gas; Lactates; Phenylketonurias; Research; Urine | 1963 |
Measurement of phenyllactate, phenylacetate, and phenylpyruvate by negative ion chemical ionization-gas chromatography/mass spectrometry in brain of mouse genetic models of phenylketonuria and non-phenylketonuria hyperphenylalaninemia.
Topics: Animals; Brain; Disease Models, Animal; Gas Chromatography-Mass Spectrometry; Humans; Lactates; Mice | 2000 |
Urinary D-4-hydroxyphenyllactate, D-phenyllactate and D-2-hydroxyisocaproate, abnormalities of bacterial origin.
Topics: Amino Acid Metabolism, Inborn Errors; Bacteria; Caproates; Child; Child, Preschool; Chromatography, | 1987 |
Gas chromatographic analysis of abnormal urinary organic acids in phenylketonuria.
Topics: Adolescent; Adult; Child; Child, Preschool; Chromatography, Gas; Female; Humans; Lactates; Male; Phe | 1985 |
Phenylalanine metabolites, attention span and hyperactivity.
Topics: Adolescent; Attention; Child; Child, Preschool; Female; Humans; Hyperkinesis; Infant; Infant, Newbor | 1985 |