glycolic acid has been researched along with Glycosuria, Renal in 1 studies
glycolic acid: RN given refers to parent cpd
glycolic acid : A 2-hydroxy monocarboxylic acid that is acetic acid where the methyl group has been hydroxylated.
Glycosuria, Renal: An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The hyperoxaluria was unresponsive to pyridoxine." | 1.29 | Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria. ( Dekker, C; Espeel, MF; Eyskens, FJ; Kerckaert, IO; Roels, F; Van Acker, KJ; Wanders, RJ, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 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 |
|---|---|
| Van Acker, KJ | 1 |
| Eyskens, FJ | 1 |
| Espeel, MF | 1 |
| Wanders, RJ | 1 |
| Dekker, C | 1 |
| Kerckaert, IO | 1 |
| Roels, F | 1 |
1 other study available for glycolic acid and Glycosuria, Renal
| Article | Year |
|---|---|
Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria.
Topics: Alanine Transaminase; Female; Gas Chromatography-Mass Spectrometry; Glycolates; Glycosuria, Renal; H | 1996 |