tyramine has been researched along with Phenylketonurias in 4 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 | 4 (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 |
|---|---|
| LEVINE, RJ | 1 |
| NIRENBERG, PZ | 1 |
| UDENFRIEND, S | 1 |
| SJOERDSMA, A | 1 |
| Edwards, DJ | 1 |
| Blau, K | 1 |
| Lejeune, J | 1 |
| Nishimura, T | 1 |
| Gjessing, LR | 1 |
4 other studies available for tyramine and Phenylketonurias
| Article | Year |
|---|---|
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 |
Analysis of phenylethylamines in biological tissues by gas-liquid chromatography with electron-capture detection.
Topics: Alcohols; Amines; Animals; Benzyl Compounds; Brain Chemistry; Chemical Phenomena; Chemistry; Chlorin | 1972 |
[A research model in some cases of mental deficiency].
Topics: Binding Sites; Humans; Intellectual Disability; Models, Biological; Phenethylamines; Phenylketonuria | 1970 |
Studies on urinary phenolic compounds in man. 3. excretion of o-tyramine.
Topics: Chromatography, Paper; Humans; In Vitro Techniques; Male; Phenylacetates; Phenylketonurias; Tyramine | 1966 |