gamma-glutamylphenylalanine 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 |
|---|---|
| Aarsen, GJ; de Bree, PK; Duran, M; Kamerling, JP; van Sprang, FJ; Wadman, SK | 1 |
1 other study(ies) available for gamma-glutamylphenylalanine and Phenylketonurias
| Article | Year |
|---|---|
Chromatographic determination and mass spectrometric identification of gamma-glutamylphenylalanine, a urinary constituent in phenylketonuria.
Topics: Adolescent; Child; Child, Preschool; Chromatography, Gas; Chromatography, Thin Layer; Dipeptides; Female; Humans; Infant; Infant, Newborn; Mass Spectrometry; Phenylalanine; Phenylketonurias | 1980 |