3,7,12-trihydroxycholestan-26-oic acid has been researched along with Adrenoleukodystrophy, Autosomal Neonatal Form in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Denis, S; Seedorf, U; van Berkel, E; Wanders, RJ; Wirtz, KW; Wouters, F | 1 |
| Jakobs, C; Johnson, DW; Schuit, RC; ten Brink, HJ | 1 |
| Denis, S; Ferdinandusse, S; Overmars, H; Vreken, P; Wanders, RJ; Waterham, HR | 1 |
3 other study(ies) available for 3,7,12-trihydroxycholestan-26-oic acid and Adrenoleukodystrophy, Autosomal Neonatal Form
| Article | Year |
|---|---|
Identification of the newly discovered 58 kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: implications for peroxisomal beta-oxidation disorders.
Topics: Acetyl-CoA C-Acetyltransferase; Carrier Proteins; Cholestanols; Fatty Acids; Humans; Microbodies; Oxidation-Reduction; Peroxisomal Disorders | 1998 |
Rapid and quantitative analysis of unconjugated C(27) bile acids in plasma and blood samples by tandem mass spectrometry.
Topics: Age Factors; Bile Acids and Salts; Child; Child, Preschool; Cholestanols; Deuterium; Fatty Acids; Humans; Infant; Infant, Newborn; Matched-Pair Analysis; Peroxisomal Disorders; Spectrometry, Mass, Electrospray Ionization | 2001 |
Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency.
Topics: Bile Acids and Salts; Child, Preschool; Cholestanols; Cholestasis, Intrahepatic; Diagnosis, Differential; Female; Humans; Infant; Male; Oxidation-Reduction; Peroxisomal Disorders; Peroxisomes; Racemases and Epimerases; Spectrometry, Mass, Electrospray Ionization; Stereoisomerism; Zellweger Syndrome | 2001 |