carnitine 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cystinuria is a rare inherited renal stone disease caused by mutations in the SLC3A1 and SLC7A9 genes." | 1.48 | Clinical, Biochemical, and Genetic Findings of Cystinuria in Chinese Children. ( Li, D; Li, XY; Liu, YP; Ma, YY; Song, JQ; Yang, YL, 2018) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ma, YY | 1 |
| Liu, YP | 1 |
| Li, D | 1 |
| Li, XY | 1 |
| Song, JQ | 1 |
| Yang, YL | 1 |
1 other study available for carnitine and Cystinuria
| Article | Year |
|---|---|
Clinical, Biochemical, and Genetic Findings of Cystinuria in Chinese Children.
Topics: Adolescent; Amino Acid Transport Systems, Basic; Amino Acid Transport Systems, Neutral; Amino Acids; | 2018 |