beta-ureidoisobutyric acid has been researched along with beta-alanine in 2 studies
Studies (beta-ureidoisobutyric acid) | Trials (beta-ureidoisobutyric acid) | Recent Studies (post-2010) (beta-ureidoisobutyric acid) | Studies (beta-alanine) | Trials (beta-alanine) | Recent Studies (post-2010) (beta-alanine) |
---|---|---|---|---|---|
11 | 2 | 4 | 3,177 | 207 | 1,807 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ishida, A; Kuhara, T; Matsuo, M; Ohse, M | 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 beta-ureidoisobutyric acid and beta-alanine
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 |
1 other study(ies) available for beta-ureidoisobutyric acid and beta-alanine
Article | Year |
---|---|
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 |