glyceric acid has been researched along with Hyperoxaluria, Primary in 9 studies
glyceric acid: found in urine of patient with D-glyceric acidemia & hyperglycinaemia; RN given refers to parent cpd without isomeric designation
glycerol ether : Any ether having glyceryl as at least one of the O-substituents.
glyceric acid : A trionic acid that consists of propionic acid substituted at positions 2 and 3 by hydroxy groups.
Hyperoxaluria, Primary: A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
| Excerpt | Relevance | Reference |
|---|---|---|
| "D-glyceric aciduria (DGA) is an autosomal recessive metabolic disorder caused by mutations in the GLYCTK gene." | 2.61 | Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review. ( Abu Rashid, M; Elpeleg, O; Eran, A; Jansen, EEW; Mandel, H; Ravid, S; Saada, A; Shaag, A; Spiegel, R; Wamelink, MMC; Zehavi, Y, 2019) |
| "This may reveal underdiagnosed primary hyperoxaluria, even in older patients." | 1.46 | Late diagnosis of primary hyperoxaluria type III. ( Acquaviva, C; Blouin, JM; Bouchet, S; de la Faille, R; Harambat, J; Llanas, B; Richard, E, 2017) |
| "D-glyceric aciduria is a rare inborn error of serine and fructose metabolism that was first described in 1974." | 1.36 | D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK). ( Chang, R; Christensen, E; Fischer, K; Kapelari, K; Sass, JO; Scholl-Bürgi, S; Walter, M; Wang, R, 2010) |
| "l-Glyceric acid was also isolated from the urine of healthy controls as one of the main peaks." | 1.33 | Differential chemical diagnosis of primary hyperoxaluria type II. Highly sensitive analysis of optical isomers of glyceric acid by GC/MS as diastereoisomeric derivatives. ( Inoue, Y; Kuhara, T; Ohse, M; Shinka, T, 2005) |
| "Type I primary hyperoxaluria (PH I) results from a deficiency of alanine:glyoxylate aminotransferase, whereas type II disease has been traced to a deficiency of D-glycerate dehydrogenase." | 1.30 | Extraction of glyceric and glycolic acids from urine with tetrahydrofuran: utility in detection of primary hyperoxaluria. ( Dietzen, DJ; Kenagy, DN; Landt, M; Milliner, DS; Smith, CH; Wilhite, TR, 1997) |
| "Most cases of primary hyperoxaluria are due to deficiency of hepatic peroxisomal alanine:glyoxylate aminotransferase [i." | 1.29 | Primary hyperoxaluria type 2. ( Mansell, MA, 1995) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (33.33) | 18.2507 |
| 2000's | 2 (22.22) | 29.6817 |
| 2010's | 4 (44.44) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Swanson, MA | 1 |
| Garcia, SM | 1 |
| Spector, E | 1 |
| Kronquist, K | 1 |
| Creadon-Swindell, G | 1 |
| Walter, M | 2 |
| Christensen, E | 2 |
| Van Hove, JLK | 1 |
| Sass, JO | 2 |
| Zehavi, Y | 1 |
| Mandel, H | 1 |
| Eran, A | 1 |
| Ravid, S | 1 |
| Abu Rashid, M | 1 |
| Jansen, EEW | 1 |
| Wamelink, MMC | 1 |
| Saada, A | 1 |
| Shaag, A | 1 |
| Elpeleg, O | 1 |
| Spiegel, R | 1 |
| Richard, E | 1 |
| Blouin, JM | 1 |
| Harambat, J | 1 |
| Llanas, B | 1 |
| Bouchet, S | 1 |
| Acquaviva, C | 1 |
| de la Faille, R | 1 |
| Fischer, K | 1 |
| Wang, R | 1 |
| Scholl-Bürgi, S | 1 |
| Chang, R | 1 |
| Kapelari, K | 1 |
| Inoue, Y | 1 |
| Shinka, T | 1 |
| Ohse, M | 1 |
| Kuhara, T | 1 |
| Rumsby, G | 1 |
| Mansell, MA | 1 |
| Dietzen, DJ | 1 |
| Wilhite, TR | 1 |
| Kenagy, DN | 1 |
| Milliner, DS | 1 |
| Smith, CH | 1 |
| Landt, M | 1 |
| Petrarulo, M | 1 |
| Marangella, M | 1 |
| Cosseddu, D | 1 |
| Linari, F | 1 |
1 review available for glyceric acid and Hyperoxaluria, Primary
| Article | Year |
|---|---|
Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review.
Topics: Brain Diseases; Child; Epilepsy; Glyceric Acids; Humans; Hyperoxaluria, Primary; Infant; Male; Mutat | 2019 |
8 other studies available for glyceric acid and Hyperoxaluria, Primary
| Article | Year |
|---|---|
d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence.
Topics: Amino Acid Oxidoreductases; Aminomethyltransferase; Carrier Proteins; Diagnosis, Differential; Epile | 2017 |
Late diagnosis of primary hyperoxaluria type III.
Topics: Aged; Carcinoma, Renal Cell; Delayed Diagnosis; Gene Expression; Glyceric Acids; Glycolates; Humans; | 2017 |
D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK).
Topics: Amino Acid Sequence; Base Sequence; Body Fluids; Child; Child, Preschool; DNA Mutational Analysis; F | 2010 |
Differential chemical diagnosis of primary hyperoxaluria type II. Highly sensitive analysis of optical isomers of glyceric acid by GC/MS as diastereoisomeric derivatives.
Topics: Diagnosis, Differential; Gas Chromatography-Mass Spectrometry; Glyceric Acids; Humans; Hyperoxaluria | 2005 |
Is liver analysis still required for the diagnosis of primary hyperoxaluria type 2?
Topics: Alcohol Oxidoreductases; Biomarkers; Biopsy; Clinical Enzyme Tests; Glyceric Acids; Hyperoxaluria, P | 2006 |
Primary hyperoxaluria type 2.
Topics: Adult; Carbohydrate Dehydrogenases; Child, Preschool; Female; Glyceric Acids; Humans; Hyperoxaluria, | 1995 |
Extraction of glyceric and glycolic acids from urine with tetrahydrofuran: utility in detection of primary hyperoxaluria.
Topics: Adolescent; Child; Child, Preschool; Chromatography, Gas; Creatinine; Furans; Glyceric Acids; Glycol | 1997 |
High-performance liquid chromatographic assay for L-glyceric acid in body fluids. Application in primary hyperoxaluria type 2.
Topics: Body Fluids; Chromatography, High Pressure Liquid; Glyceric Acids; Humans; Hydrogen-Ion Concentratio | 1992 |