beta-methylcrotonylglycine has been researched along with Metabolism, Inborn Errors in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kluijtmans, LAJ; Koene, S; Mock, D; Morava, E; Pasch, M; Wevers, R | 1 |
| Baumgartner, MR; Baykal, T; Can, G; Dantas, MF; Demir, F; Demirkol, M; Fowler, B; Gokcay, GH; Ince, Z | 1 |
| Barshop, BA; Baumgartner, MR; Chambaz, C; Cropcho, LJ; Finegold, DN; Gibson, KM; Koch, HG; Matern, D; Suormala, T; Vockley, J; Walters, N; Wolfe, LA | 1 |
| Berry, SA; Nyhan, WL; Thuy, LP; Tuchman, M | 1 |
| Hähnel, R; Wysocki, SJ | 1 |
5 other study(ies) available for beta-methylcrotonylglycine and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delay.
Topics: Abnormalities, Multiple; Aging, Premature; Biotin; Child, Preschool; Developmental Disabilities; Ectoderm; Female; Glycine; Growth Disorders; Humans; Metabolism, Inborn Errors | 2008 |
Consanguineous 3-methylcrotonyl-CoA carboxylase deficiency: early-onset necrotizing encephalopathy with lethal outcome.
Topics: Carbon-Carbon Ligases; Consanguinity; Diagnosis, Differential; Fatal Outcome; Glycine; Humans; Infant; Infant, Newborn; Leukoencephalitis, Acute Hemorrhagic; Male; Metabolism, Inborn Errors; Mutation; RNA Splice Sites; Valerates | 2005 |
Potential misdiagnosis of 3-methylcrotonyl-coenzyme A carboxylase deficiency associated with absent or trace urinary 3-methylcrotonylglycine.
Topics: Carbon-Carbon Ligases; Child; Diagnostic Errors; Female; Glycine; Humans; Infant; Metabolism, Inborn Errors; Mutation, Missense | 2007 |
Partial methylcrotonyl-coenzyme A carboxylase deficiency in an infant with failure to thrive, gastrointestinal dysfunction, and hypertonia.
Topics: Biotin; Carbon-Carbon Ligases; Failure to Thrive; Gastrointestinal Diseases; Glycine; Humans; Infant; Ligases; Male; Metabolism, Inborn Errors; Muscle Hypertonia; Valerates | 1993 |
3-Methylcrotonylglycine excretion in 3-hydroxy-3-methylglutaric aciduria.
Topics: Crotonates; Glutarates; Glycine; Humans; Hydroxy Acids; Infant; Male; Metabolism, Inborn Errors | 1978 |