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glyceric acid and Hyperoxaluria

glyceric acid has been researched along with Hyperoxaluria in 5 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: Excretion of an excessive amount of OXALATES in the urine.

Research Excerpts

ExcerptRelevanceReference
"Primary hyperoxaluria (PH) type 1 and type 2 are autosomal recessive defects of oxalate metabolism resulting from glyoxylate accumulation which occurs by two distinct pathways."5.29Detection of primary hyperoxaluria type 2 (L-glyceric aciduria) in patients with maintained renal function or end-stage renal failure. ( Barbos, MP; Cadario, A; Cosseddu, D; Gurioli, L; Linari, F; Marangella, M; Petrarulo, M; Vitale, C, 1995)
"Primary hyperoxaluria (PH) type 1 and type 2 are autosomal recessive defects of oxalate metabolism resulting from glyoxylate accumulation which occurs by two distinct pathways."1.29Detection of primary hyperoxaluria type 2 (L-glyceric aciduria) in patients with maintained renal function or end-stage renal failure. ( Barbos, MP; Cadario, A; Cosseddu, D; Gurioli, L; Linari, F; Marangella, M; Petrarulo, M; Vitale, C, 1995)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's3 (60.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Marangella, M1
Petrarulo, M1
Cosseddu, D1
Vitale, C1
Cadario, A1
Barbos, MP1
Gurioli, L1
Linari, F1
Sönmez, F1
Mir, S1
Cura, A1
Raghavan, KG1
Lathika, KM1
Gandhi, NM1
D'Souza, SJ1
Tarachand, U1
Ramakrishnan, V1
Singh, BB1
Rumsby, G1
Sharma, A1
Cregeen, DP1
Solomon, LR1
Blakemore, WF1
Heath, MF1
Bennett, MJ1
Cromby, CH1
Pollitt, RJ1

Other Studies

5 other studies available for glyceric acid and Hyperoxaluria

ArticleYear
Detection of primary hyperoxaluria type 2 (L-glyceric aciduria) in patients with maintained renal function or end-stage renal failure.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 1995, Volume: 10, Issue:8

    Topics: Child, Preschool; Female; Glyceric Acids; Glycolates; Humans; Hyperoxaluria; Kidney Failure, Chronic

1995
Nephrocalcinosis in a patient with primary hyperoxaluria type 2.
    Pediatric nephrology (Berlin, Germany), 1997, Volume: 11, Issue:2

    Topics: Child; Child, Preschool; Glyceric Acids; Humans; Hyperoxaluria; Infant; Nephrocalcinosis

1997
Biogenesis of L-glyceric aciduria, oxalosis and renal injury in rats simulating type II primary hyperoxaluria.
    Biochimica et biophysica acta, 1997, Dec-31, Volume: 1362, Issue:2-3

    Topics: Animals; Glyceric Acids; Glyoxylates; Hyperoxaluria; Kidney Diseases; L-Lactate Dehydrogenase; Lipid

1997
Primary hyperoxaluria type 2 without L-glycericaciduria: is the disease under-diagnosed?
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2001, Volume: 16, Issue:8

    Topics: Alcohol Oxidoreductases; Glyceric Acids; Humans; Hydroxypyruvate Reductase; Hyperoxaluria; Kidney Ca

2001
Primary hyperoxaluria and L-glyceric aciduria in the cat.
    Journal of inherited metabolic disease, 1988, Volume: 11 Suppl 2

    Topics: Acute Kidney Injury; Animals; Cat Diseases; Cats; Disease Models, Animal; Female; Glyceric Acids; Hy

1988