urea has been researched along with Acidemia Propionic in 5 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
Excerpt | Relevance | Reference |
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"The objective of this study was to determine whether N-carbamylglutamate (NCG) reduces plasma levels of ammonia and glutamine and increases the rate of ureagenesis in patients with propionic acidemia (PA)." | 9.14 | N-carbamylglutamate augments ureagenesis and reduces ammonia and glutamine in propionic acidemia. ( Ah Mew, N; Daikhin, Y; McCarter, R; Nissim, I; Tuchman, M; Yudkoff, M, 2010) |
"The objective of this study was to determine whether N-carbamylglutamate (NCG) reduces plasma levels of ammonia and glutamine and increases the rate of ureagenesis in patients with propionic acidemia (PA)." | 5.14 | N-carbamylglutamate augments ureagenesis and reduces ammonia and glutamine in propionic acidemia. ( Ah Mew, N; Daikhin, Y; McCarter, R; Nissim, I; Tuchman, M; Yudkoff, M, 2010) |
"Life-threatening hyperammonemia occurs in both inherited and acquired liver diseases affecting ureagenesis, the main pathway for detoxification of neurotoxic ammonia in mammals." | 4.12 | O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis. ( Arena, P; Attanasio, S; Boffa, I; Brunetti-Pierri, N; Cuomo, P; D'Alessio, AM; De Angelis, A; Desviat, LR; Ferenbach, AT; Häberle, J; Lipshutz, GS; Makris, G; Martínez-Pizarro, A; Motta, A; Nitzahn, M; Nusco, E; Paris, D; Pravata, VM; Richard, E; Rüfenacht, V; Soria, LR; van Aalten, DMF, 2022) |
"Propionic acidemia is an inborn error of metabolism caused by a deficiency in the mitochondrial enzyme propionyl-CoA carboxylase that converts the propionyl CoA to methyl malonyl CoA." | 1.72 | Interorgan amino acid interchange in propionic acidemia: the missing key to understanding its physiopathology. ( Arrieta, F; Belanger-Quintana, A; Del Valle, M; Fernandez-Felix, BM; Garcia, F; Martinez-Pardo, M; Ruiz-Sala, P; Stanescu, S, 2022) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (60.00) | 24.3611 |
2020's | 2 (40.00) | 2.80 |
Authors | Studies |
---|---|
Stanescu, S | 1 |
Belanger-Quintana, A | 1 |
Fernandez-Felix, BM | 1 |
Ruiz-Sala, P | 1 |
Del Valle, M | 1 |
Garcia, F | 1 |
Arrieta, F | 1 |
Martinez-Pardo, M | 1 |
Soria, LR | 1 |
Makris, G | 1 |
D'Alessio, AM | 1 |
De Angelis, A | 1 |
Boffa, I | 1 |
Pravata, VM | 1 |
Rüfenacht, V | 1 |
Attanasio, S | 1 |
Nusco, E | 1 |
Arena, P | 1 |
Ferenbach, AT | 1 |
Paris, D | 1 |
Cuomo, P | 1 |
Motta, A | 1 |
Nitzahn, M | 1 |
Lipshutz, GS | 1 |
Martínez-Pizarro, A | 1 |
Richard, E | 1 |
Desviat, LR | 1 |
Häberle, J | 1 |
van Aalten, DMF | 1 |
Brunetti-Pierri, N | 1 |
Chapman, KA | 1 |
Collado, MS | 1 |
Figler, RA | 1 |
Hoang, SA | 1 |
Armstrong, AJ | 1 |
Cui, W | 1 |
Purdy, M | 1 |
Simmers, MB | 1 |
Yazigi, NA | 1 |
Summar, ML | 1 |
Wamhoff, BR | 1 |
Dash, A | 1 |
Ah Mew, N | 1 |
McCarter, R | 1 |
Daikhin, Y | 1 |
Nissim, I | 1 |
Yudkoff, M | 1 |
Tuchman, M | 1 |
Scholl-Bürgi, S | 1 |
Sass, JO | 1 |
Zschocke, J | 1 |
Karall, D | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Increasing Ureagenesis in Inborn Errors of Metabolism With N-Carbamylglutamate[NCT01341379] | Phase 2 | 0 participants (Actual) | Interventional | 2010-12-31 | Withdrawn (stopped due to Lack of funding) | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
1 review available for urea and Acidemia Propionic
Article | Year |
---|---|
Amino acid metabolism in patients with propionic acidaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Ammonia; Citric Acid Cycle; Diet; | 2012 |
1 trial available for urea and Acidemia Propionic
Article | Year |
---|---|
N-carbamylglutamate augments ureagenesis and reduces ammonia and glutamine in propionic acidemia.
Topics: Administration, Oral; Adolescent; Ammonia; Blood Chemical Analysis; Child; Child, Preschool; Confide | 2010 |
3 other studies available for urea and Acidemia Propionic
Article | Year |
---|---|
Interorgan amino acid interchange in propionic acidemia: the missing key to understanding its physiopathology.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Glutamine; Humans; Hyperammonem | 2022 |
O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis.
Topics: Acetylglucosamine; Ammonia; Animals; Biocatalysis; Carbamoyl-Phosphate Synthase (Ammonia); Disease M | 2022 |
Recapitulation of metabolic defects in a model of propionic acidemia using patient-derived primary hepatocytes.
Topics: Actins; Amino Acids, Branched-Chain; Ammonia; Carbon-Carbon Ligases; Cells, Cultured; Child; Fibrobl | 2016 |