urea has been researched along with phenylacetylglutamine in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 4 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brusilow, SW | 1 |
| Bergström, J; Jörnvall, H; Zimmerman, L | 1 |
| Brusilow, SW; Rajantie, J; Simell, O; Sipilä, I; Valle, DL | 1 |
| Batshaw, ML; Brusilow, SW; Thomas, GH | 1 |
| Chandramouli, V; Ekberg, K; Kalhan, SC; Kumaran, K; Landau, BR; Schumann, WC; Wahren, J | 1 |
| Brusilow, SW; Finkelstien, J | 1 |
| Alexeeva, O; Baranovsky, A; Bass, NM; Brown, RS; Coakley, D; Dickinson, K; Dudar, L; Fadieienko, G; Ghabril, M; Grewal, P; Grinevich, V; Kharchenko, N; Klaryts'ka, I; Mantry, P; McCashland, T; Mokhtarani, M; Morozov, V; Norris, C; Reddy, KG; Reddy, KR; Rockey, DC; Scharschmidt, BF; Syplyviy, V; Vierling, JM; Zupanets, IA | 1 |
| Almannai, M; Elsea, SH; Jiang, Y; Sun, Q; Sutton, VR | 1 |
1 trial(s) available for urea and phenylacetylglutamine
| Article | Year |
|---|---|
Randomized, double-blind, controlled study of glycerol phenylbutyrate in hepatic encephalopathy.
Topics: Adult; Aged; Ammonia; Double-Blind Method; Female; Glutamine; Glycerol; Hepatic Encephalopathy; Humans; Hyperammonemia; Male; Middle Aged; Phenylbutyrates; Treatment Outcome; Urea; Young Adult | 2014 |
7 other study(ies) available for urea and phenylacetylglutamine
| Article | Year |
|---|---|
Phenylacetylglutamine may replace urea as a vehicle for waste nitrogen excretion.
Topics: Adolescent; Child; Child, Preschool; Female; Glutamine; Humans; Infant; Male; Metabolism, Inborn Errors; Nitrogen; Phenylacetates; Phenylbutyrates; Urea | 1991 |
Phenylacetylglutamine and hippuric acid in uremic and healthy subjects.
Topics: Blood Proteins; Creatinine; Glutamine; Hippurates; Humans; Kidney; Metabolic Clearance Rate; Protein Binding; Urea; Uremia | 1990 |
Waste nitrogen excretion via amino acid acylation: benzoate and phenylacetate in lysinuric protein intolerance.
Topics: Acylation; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Benzoates; Benzoic Acid; Child; Child, Preschool; Creatinine; Glutamine; Hippurates; Humans; Lysine; Nitrogen; Orotic Acid; Phenylacetates; Urea | 1986 |
New approaches to the diagnosis and treatment of inborn errors or urea synthesis.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinic Acid; Citrulline; Glutamine; Hippurates; Humans; Infant; Infant, Newborn; Phenylacetates; Urea | 1981 |
Estimates of Krebs cycle activity and contributions of gluconeogenesis to hepatic glucose production in fasting healthy subjects and IDDM patients.
Topics: Adult; Bicarbonates; Blood Glucose; Carbon Radioisotopes; Case-Control Studies; Citric Acid Cycle; Diabetes Mellitus, Type 1; Fasting; Female; Gluconeogenesis; Glutamic Acid; Glutamine; Humans; Kinetics; Lactates; Liver; Male; Models, Biological; Radioisotope Dilution Technique; Reference Values; Urea | 1995 |
Restoration of nitrogen homeostasis in a man with ornithine transcarbamylase deficiency.
Topics: Adult; Arginine; Glutamine; Homeostasis; Humans; Male; Nitrogen; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phenylbutyrates; Quaternary Ammonium Compounds; Urea | 1993 |
Quantitation of phenylbutyrate metabolites by UPLC-MS/MS demonstrates inverse correlation of phenylacetate:phenylacetylglutamine ratio with plasma glutamine levels.
Topics: Ammonia; Argininosuccinic Aciduria; Chromatography, Liquid; Female; Glutamine; Glycerol; Humans; Limit of Detection; Male; Middle Aged; Ornithine Carbamoyltransferase Deficiency Disease; Phenylacetates; Phenylbutyrates; Tandem Mass Spectrometry; Urea; Urea Cycle Disorders, Inborn | 2017 |