n-carbamoyl-beta-alanine has been researched along with urea in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (40.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (40.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ahlemeyer, B; Assmann, B; Exner-Camps, S; Hoffmann, GF; Hörster, F; Kohlmüller, D; Kölker, S; Krieglstein, J; Mayatepek, E; Okun, JG | 1 |
Ishida, A; Kuhara, T; Matsuo, M; Ohse, M | 1 |
FRITZSON, P | 1 |
FRITZSON, P; PIHL, A | 1 |
Chan, B; Chan, KY; Lai, CK; Lam, CW; Law, CY; Leung, KF; Mak, CM; Pak-lam Chen, S; Yan-wo Chan, A; Yuen, YP | 1 |
1 trial(s) available for n-carbamoyl-beta-alanine and urea
Article | Year |
---|---|
Screening and diagnosis of beta-ureidopropionase deficiency by gas chromatographic/mass spectrometric analysis of urine.
Topics: Amidohydrolases; beta-Alanine; Calibration; Gas Chromatography-Mass Spectrometry; Humans; Indicators and Reagents; Infant, Newborn; Magnetic Resonance Spectroscopy; Neonatal Screening; Pilot Projects; Purine-Pyrimidine Metabolism, Inborn Errors; Pyrimidines; Reproducibility of Results; Urea; Urease | 2002 |
4 other study(ies) available for n-carbamoyl-beta-alanine and urea
Article | Year |
---|---|
3-Ureidopropionate contributes to the neuropathology of 3-ureidopropionase deficiency and severe propionic aciduria: a hypothesis.
Topics: Animals; beta-Alanine; Brain Diseases, Metabolic; Calcium; Cell Death; Cells, Cultured; Central Nervous System; Chick Embryo; Citrulline; Electron Transport; Energy Metabolism; Enzyme Inhibitors; Excitatory Amino Acid Antagonists; Formamides; Glutamic Acid; Mitochondria; Neurons; Neurotoxins; Oxidative Stress; Propionates; Reactive Oxygen Species; Receptors, N-Methyl-D-Aspartate; Urea | 2001 |
The catabolism of C14-labeled uracil, dihydrouracil, and beta-ureidopropionic acid in rat liver slices.
Topics: Alanine; Animals; beta-Alanine; Liver; Rats; Uracil; Urea | 1957 |
The catabolism of C14-labeled uracil, dihydrouracil, and beta-ureidopropionic acid in the intact rat.
Topics: Alanine; Animals; beta-Alanine; Rats; Uracil; Urea | 1957 |
NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome.
Topics: Abnormalities, Multiple; Amidohydrolases; beta-Alanine; Brain Diseases; Epilepsies, Myoclonic; Gas Chromatography-Mass Spectrometry; Homozygote; Humans; Infant; Magnetic Resonance Spectroscopy; Male; Movement Disorders; NAV1.1 Voltage-Gated Sodium Channel; Purine-Pyrimidine Metabolism, Inborn Errors; Urea; Urinalysis | 2015 |