atrolactic acid has been researched along with Phenylketonurias in 2 studies
atrolactic acid: see also 3-isomer; RN given refers to parent cpd without isomeric designation; structure
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 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 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 |
|---|---|
| Langenbeck, U | 1 |
| Behbehani, A | 1 |
| Mench-Hoinowski, A | 1 |
| Clemens, PC | 1 |
| Schünemann, MH | 1 |
| Hoffmann, GF | 1 |
| Kohlschütter, A | 1 |
2 other studies available for atrolactic acid and Phenylketonurias
| Article | Year |
|---|---|
A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria.
Topics: Adolescent; Child; Child, Preschool; Female; Humans; Kidney; Lactates; Male; Phenylacetates; Phenyla | 1992 |
Plasma concentrations of phenyllactic acid in phenylketonuria.
Topics: Adolescent; Adult; Child; Child, Preschool; Food, Formulated; Humans; Infant; Lactates; Phenylalanin | 1990 |