carnitine has been researched along with 3-methylglutaconic acid in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gibson, KM; Lee, CF; Wappner, RS | 1 |
| de Wet, WJ; Erasmus, E; Gibson, KM; Jooste, S; Mienie, LJ | 1 |
| Armstrong, DL; Scaglia, F; Scheuerle, AE; Sweetman, L; Towbin, JA; Wong, LJ | 1 |
| Buckel, W; Carpenter, K; Ensenauer, R; Gibson, KM; Hoffmann, GF; Liesert, M; Ly, TB; Mack, M; Peters, V; Wilcken, B; Zschocke, J | 1 |
4 other study(ies) available for carnitine and 3-methylglutaconic acid
| Article | Year |
|---|---|
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.
Topics: Carnitine; Diseases in Twins; Fibroblasts; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Lymphocytes; Male; Meglutol | 1992 |
The detection of 3-methylglutarylcarnitine and a new dicarboxylic conjugate, 3-methylglutaconylcarnitine, in 3-methylglutaconic aciduria.
Topics: Acidosis; Carnitine; Chromatography, Gas; Female; Fibroblasts; Glutarates; Glycine; Humans; Hydro-Lyases; Infant; Male; Spectrometry, Mass, Fast Atom Bombardment | 1994 |
Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism.
Topics: Biomarkers; Carnitine; DNA, Mitochondrial; Female; Glutarates; Humans; Infant, Newborn; Mitochondrial Myopathies; Mutation; Orotic Acid; Reye Syndrome; Tachycardia, Ventricular | 2002 |
Mutations in the AUH gene cause 3-methylglutaconic aciduria type I.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Exons; Genes, Recessive; Glutarates; Humans; Hydro-Lyases; Infant, Newborn; Intellectual Disability; Language Development Disorders; Male; Mutation; Neonatal Screening | 2003 |