n-acetylphenylalanine has been researched along with Phenylketonurias in 2 studies
N-acetylphenylalanine: RN given refers to (DL)-isomer
N-acetylphenylalanine : The N-acetyl derivative of phenylalanine.
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).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Urinary organic acid profiles of patients with Maple Syrup Urine Disease (MSUD), hereditary tyrosinemia and phenylketonuria (PKU) have been studied by means of capillary GC-MS-computer technique." | 3.67 | Urinary excretion of N-acetyl amino acids in patients with some inborn errors of amino acid metabolism. ( Horn, L; Jellum, E; Kvittingen, EA; Stokke, O; Thoresen, O, 1986) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (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 |
|---|---|
| Jellum, E | 1 |
| Horn, L | 1 |
| Thoresen, O | 1 |
| Kvittingen, EA | 1 |
| Stokke, O | 1 |
| Okajima, K | 1 |
| Inoue, M | 1 |
| Morino, Y | 1 |
2 other studies available for n-acetylphenylalanine and Phenylketonurias
| Article | Year |
|---|---|
Urinary excretion of N-acetyl amino acids in patients with some inborn errors of amino acid metabolism.
Topics: Acetylation; Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Gas Chromatography-M | 1986 |
Studies on the mechanism for renal elimination of N-acetylphenylalanine: its pathophysiologic significance in phenylketonuria.
Topics: Animals; Humans; Kidney; Ligation; Male; Nephrectomy; Phenylalanine; Phenylketonurias; Probenecid; P | 1985 |