tyramine has been researched along with Cystinuria in 1 studies
Cystinuria: An inherited disorder due to defective reabsorption of CYSTINE and other BASIC AMINO ACIDS by the PROXIMAL RENAL TUBULES. This form of aminoaciduria is characterized by the abnormally high urinary levels of cystine; LYSINE; ARGININE; and ORNITHINE. Mutations involve the amino acid transport protein gene SLC3A1.
| 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 |
|---|---|
| TOMPSETT, SL | 1 |
1 other study available for tyramine and Cystinuria
| Article | Year |
|---|---|
The use of a cation-exchange resin in the determination of some basic substances (tyrosine, tyramine, kynurenine, 3-hydroxykynurenine and cystine) in urine.
Topics: Body Fluids; Cations; Cystinuria; Humans; Ion Exchange Resins; Kynurenine; Tyramine; Tyrosine | 1962 |