aspartyl-phenylalanine 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 | 0 (0.00) | 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 | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abeln, D; de Blaauw, P; Heiner-Fokkema, MR; Maatman, RGHJ; Melis, ES; van Dam, E; van Spronsen, FJ; van Vliet, K | 1 |
1 other study(ies) available for aspartyl-phenylalanine and Phenylketonurias
| Article | Year |
|---|---|
Aspartame and Phe-Containing Degradation Products in Soft Drinks across Europe.
Topics: Aspartame; Carbonated Beverages; Chromatography, Liquid; Diketopiperazines; Dipeptides; Europe; Food Safety; Humans; Limit of Detection; Phenylalanine; Phenylketonurias; Reproducibility of Results; Tandem Mass Spectrometry | 2020 |