oxalic acid has been researched along with Inborn Errors of Metabolism in 9 studies
Oxalic Acid: A strong dicarboxylic acid occurring in many plants and vegetables. It is produced in the body by metabolism of glyoxylic acid or ascorbic acid. It is not metabolized but excreted in the urine. It is used as an analytical reagent and general reducing agent.
oxalic acid : An alpha,omega-dicarboxylic acid that is ethane substituted by carboxyl groups at positions 1 and 2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Primary hyperoxaluria is a rare hereditary disease." | 2.39 | [Primary hyperoxaluria]. ( De Pauw, L; Toussaint, C, 1996) |
| "However, the clinical significance of recurrence is often minor." | 2.37 | [Recurrence of the original disease in the transplanted kidney]. ( Briner, J; Leumann, EP, 1984) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (77.78) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Jungers, P | 1 |
| Joly, D | 1 |
| Blanchard, A | 1 |
| Courbebaisse, M | 1 |
| Knebelmann, B | 1 |
| Daudon, M | 1 |
| Leumann, EP | 1 |
| Briner, J | 1 |
| Groth, CG | 1 |
| Ringdén, O | 1 |
| Chesney, RW | 1 |
| Friedman, AL | 1 |
| Breed, AL | 1 |
| Langer, LO | 1 |
| Gilbert, EF | 1 |
| Opitz, JM | 1 |
| De Pauw, L | 1 |
| Toussaint, C | 1 |
| Greter, J | 1 |
| Jacobson, CE | 1 |
| Baĭgil'dina, LM | 1 |
| Mitwalli, A | 1 |
| Oreopoulos, DG | 1 |
| Yendt, ER | 1 |
| Cohanim, M | 1 |
5 reviews available for oxalic acid and Inborn Errors of Metabolism
| Article | Year |
|---|---|
[Inherited monogenic kidney stone diseases: recent diagnostic and therapeutic advances].
Topics: Humans; Hyperoxaluria; Incidence; Kidney Calculi; Kidney Tubules; Metabolism, Inborn Errors; Oxalic | 2008 |
[Recurrence of the original disease in the transplanted kidney].
Topics: Anti-Glomerular Basement Membrane Disease; Glomerulonephritis; Glomerulosclerosis, Focal Segmental; | 1984 |
Transplantation in relation to the treatment of inherited disease.
Topics: alpha 1-Antitrypsin Deficiency; Amyloidosis; Bone Marrow Transplantation; Fabry Disease; Gaucher Dis | 1984 |
[Primary hyperoxaluria].
Topics: Biopsy; Diet; Glycolates; Glyoxylates; Humans; Hyperoxaluria, Primary; Ilium; Metabolism, Inborn Err | 1996 |
Hyperoxaluria and hyperoxalemia: one more concern for the nephrologist.
Topics: Ascorbic Acid; Humans; Kidney; Kidney Failure, Chronic; Kidney Transplantation; Metabolism, Inborn E | 1985 |
4 other studies available for oxalic acid and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Renal failure with hypercalcemia, renal stones, multiple pathologic fractures, and growth failure.
Topics: Child, Preschool; Female; Fractures, Spontaneous; Growth Disorders; Humans; Hypercalcemia; Kidney Ca | 1983 |
Urinary organic acids: isolation and quantification for routine metabolic screening.
Topics: Acetates; Carboxylic Acids; Cinnamates; Citrates; Citric Acid; Gas Chromatography-Mass Spectrometry; | 1987 |
[Metabolic nephropathy with oxalate-calcium crystalluria in children].
Topics: Calcium; Child; Crystallization; Humans; Kidney Diseases; Kidney Function Tests; Metabolism, Inborn | 1985 |
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 |