tyramine has been researched along with Alkaptonuria in 1 studies
Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.
| 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 |
|---|---|
| Gjessing, LR | 1 |
| Borud, O | 1 |
1 other study available for tyramine and Alkaptonuria
| Article | Year |
|---|---|
Studies on urinary phenolic compounds in man. IV. O-Tyrosine and its metabolites.
Topics: Alkaptonuria; Humans; In Vitro Techniques; Lactates; Male; Phenylacetates; Phenylalanine; Tyramine; | 1966 |