acetone has been researched along with Cystinuria in 3 studies
methyl ketone : A ketone of formula RC(=O)CH3 (R =/= H).
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 | 3 (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 |
|---|---|
| Georges, RJ | 1 |
| Politzer, WM | 1 |
| Kutter, D | 1 |
| Hyánek, J | 1 |
| Hyánková, E | 1 |
| Cafourková, Z | 1 |
| Vanĕcková, V | 1 |
3 other studies available for acetone and Cystinuria
| Article | Year |
|---|---|
pH dependency of the cyanide-nitroprusside colour reaction of cystine.
Topics: Acetone; Cyanides; Cysteine; Cystine; Cystinuria; Ferricyanides; Humans; Hydrogen-Ion Concentration | 1970 |
[Diagnostic results of complete urine analysis].
Topics: Acetone; Clinical Laboratory Techniques; Cystinuria; Glycosuria; Hematuria; Humans; Hydrogen-Ion Con | 1968 |
[Our experiences with a screening test for cystinuria and aminoaciduria].
Topics: Acetone; Cystinuria; Humans; Metabolic Diseases; Urine | 1965 |