phenethylamine has been researched along with Phenylketonurias in 3 studies
phenethylamine: RN given refers to parent cpd; structure in Merck Index, 9th ed, #7016
2-phenylethylamine : A phenylethylamine having the phenyl substituent at the 2-position.
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 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| OATES, JA | 1 |
| NIRENBERG, PZ | 2 |
| JEPSON, JB | 1 |
| SJOERDSMA, A | 2 |
| UDENFRIEND, S | 2 |
| LEVINE, RJ | 1 |
| Ghozlan, A | 1 |
| Varoquaux, O | 1 |
| Abadie, V | 1 |
3 other studies available for phenethylamine and Phenylketonurias
| Article | Year |
|---|---|
Conversion of phenylalanine to phenethylamine in patients with phenylketonuria.
Topics: Ethylamines; Humans; Phenethylamines; Phenylalanine; Phenylketonurias | 1963 |
URINARY EXCRETION OF PHENETHYLAMINE AND TYRAMINE IN NORMAL SUBJECTS AND HETEROZYGOUS CARRIERS OF PHENYLKETONURIA.
Topics: Body Fluids; Carrier State; Child; Clinical Laboratory Techniques; Ethylamines; Genetics, Medical; P | 1964 |
Is monoamine oxydase-B a modifying gene and phenylethylamine a harmful compound in phenylketonuria?
Topics: Adult; Child; Female; Humans; Infant, Newborn; Male; Monoamine Oxidase; Phenethylamines; Phenylalani | 2004 |