glycolic acid has been researched along with Inborn Errors of Metabolism in 3 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The primary hyperoxalurias are a group of recessive kidney diseases, characterised by extensive accumulation of calcium oxalate that progressively coalesces into kidney stones." | 1.40 | Mutations in HAO1 encoding glycolate oxidase cause isolated glycolic aciduria. ( Bargal, R; Belostotsky, R; Frishberg, Y; Lyakhovetsky, R; Zeharia, A, 2014) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Frishberg, Y | 1 |
| Zeharia, A | 1 |
| Lyakhovetsky, R | 1 |
| Bargal, R | 1 |
| Belostotsky, R | 1 |
| Fraser, AD | 1 |
| Yendt, ER | 1 |
| Cohanim, M | 1 |
3 other studies available for glycolic acid and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Mutations in HAO1 encoding glycolate oxidase cause isolated glycolic aciduria.
Topics: Adrenal Insufficiency; Alcohol Oxidoreductases; Child; Esophageal Achalasia; Glycolates; Glyoxylates | 2014 |
Ethylene glycol, glycolic acid, and metabolic acidosis of unknown origin.
Topics: Acidosis; Diagnosis, Differential; Ethylene Glycol; Ethylene Glycols; Glycolates; Humans; Infant; Me | 1993 |
Response to a physiologic dose of pyridoxine in type I primary hyperoxaluria.
Topics: Child; Female; Glycolates; Humans; Kidney Calculi; Metabolism, Inborn Errors; Oxalates; Oxalic Acid; | 1985 |