cystamine has been researched along with Cystinuria in 2 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 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fermo, I | 1 |
| Arcelloni, C | 1 |
| Paroni, R | 1 |
| Bremer, HJ | 1 |
| Kohne, E | 1 |
2 other studies available for cystamine and Cystinuria
| Article | Year |
|---|---|
High-performance liquid chromatographic method to quantify total cysteine excretion in urine.
Topics: Adolescent; Adult; Aged; Amino Acids, Diamino; Borohydrides; Calibration; Case-Control Studies; Chro | 2002 |
The excretion of diamines in human urine. II. Cadaverine, putrescine, 1,3-diaminopropane, 2,2'-dithiobis(ethylamine) and spermidine in urine of patients with cystinuria and cystinlysinuria.
Topics: Adult; Amines; Autoanalysis; Butylamines; Chemistry, Clinical; Child; Chromatography, Ion Exchange; | 1971 |