taurine has been researched along with Phenylketonurias in 3 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).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (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 |
|---|---|
| Broquist, HP | 1 |
| Acosta, PB | 1 |
| Stepnick-Gropper, S | 1 |
| Heathcote, JG | 1 |
| Davies, DM | 1 |
| Haworth, C | 1 |
| Oliver, RW | 1 |
1 review available for taurine and Phenylketonurias
| Article | Year |
|---|---|
Amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Biological Transport, Active; Carnitine; | 1976 |
2 other studies available for taurine and Phenylketonurias
| Article | Year |
|---|---|
Problems related to diet management of maternal phenylketonuria.
Topics: alpha-Linolenic Acid; Carnitine; Cations, Divalent; Cell Membrane Permeability; Cholesterol; Dietary | 1986 |
An improved technique for the analysis of amino acids and related compounds on thin layers of cellulose. IV. The quantitative determination of amino acids in urine.
Topics: Amino Acid Metabolism, Inborn Errors; Autoanalysis; Cellulose; Child; Chromatography, Ion Exchange; | 1971 |