beta-methylcrotonylglycine has been researched along with 3-hydroxyisovalerylcarnitine in 2 studies
| Studies (beta-methylcrotonylglycine) | Trials (beta-methylcrotonylglycine) | Recent Studies (post-2010) (beta-methylcrotonylglycine) | Studies (3-hydroxyisovalerylcarnitine) | Trials (3-hydroxyisovalerylcarnitine) | Recent Studies (post-2010) (3-hydroxyisovalerylcarnitine) |
|---|---|---|---|---|---|
| 27 | 0 | 4 | 26 | 2 | 18 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Berry, SA; Gage, DA; Huang, ZH; Iwamoto, T; Johnston, K; Millington, DS; Packman, S; Röschinger, W; Sweetman, L; Yano, S | 1 |
| Baumgartner, MR; Burda, P; Bürer, C; Fowler, B; Grünert, SC; Morscher, RJ; Suormala, T | 1 |
2 other study(ies) available for beta-methylcrotonylglycine and 3-hydroxyisovalerylcarnitine
| Article | Year |
|---|---|
3-Hydroxyisovalerylcarnitine in patients with deficiency of 3-methylcrotonyl CoA carboxylase.
Topics: Carbon-Carbon Ligases; Carnitine; Child, Preschool; Female; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Ligases; Male; Valerates | 1995 |
A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency.
Topics: Acyl Coenzyme A; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child; Child, Preschool; DNA Mutational Analysis; Female; Fibroblasts; Glycine; Heterozygote; Humans; Infant; Infant, Newborn; Male; Mutation; Neonatal Screening; Real-Time Polymerase Chain Reaction; Skin; Urea Cycle Disorders, Inborn | 2012 |