s-adenosylmethionine has been researched along with Adrenoleukodystrophy, Autosomal Neonatal Form in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Bhadane, P; Dahal, R; Jangam, S; Lesko, B; McPheron, M; Miller, MJ; Wangler, MF; Wilson, TE | 1 |
| Ferdinandusse, S; Herzog, K; van Lenthe, H; Vaz, FM; Wanders, RJA; Waterham, HR | 1 |
| Boenzi, S; Carrozzo, R; Di Ciommo, V; Dionisi-Vici, C; Duranti, G; Johnson, DW; Meschini, MC; Ravà, L; Rizzo, C | 1 |
| Hubbard, WC; Jones, RO; Kratz, LE; Moser, AB; Raymond, GV; Sandlers, Y | 1 |
| Boenzi, S; Caruso, U; Dionisi-Vici, C; Duran, M; Rizzo, C; Wanders, RJ | 1 |
| Jakobs, C; Roe, CR; ten Brink, HJ; Verhoeven, NM; Wanders, RJ | 1 |
| Carpenter, KH; Wiley, V | 1 |
1 review(s) available for s-adenosylmethionine and Adrenoleukodystrophy, Autosomal Neonatal Form
| Article | Year |
|---|---|
Application of tandem mass spectrometry to biochemical genetics and newborn screening.
Topics: Amino Acids; Carnitine; Genetic Testing; Humans; Infant, Newborn; Molecular Biology; Neonatal Screening; Peroxisomal Disorders; Spectrometry, Mass, Electrospray Ionization | 2002 |
6 other study(ies) available for s-adenosylmethionine and Adrenoleukodystrophy, Autosomal Neonatal Form
| Article | Year |
|---|---|
Dicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders.
Topics: Adrenoleukodystrophy; ATPases Associated with Diverse Cellular Activities; Biomarkers; Chromatography, Liquid; Humans; Infant, Newborn; Membrane Proteins; Peroxisomal Disorders; Tandem Mass Spectrometry | 2023 |
Identification and diagnostic value of phytanoyl- and pristanoyl-carnitine in plasma from patients with peroxisomal disorders.
Topics: Carnitine; Cells, Cultured; Diterpenes; Fatty Acids; Humans; Oxidation-Reduction; Peroxisomal Disorders; Phytanic Acid; Refsum Disease | 2017 |
Urine acylcarnitine analysis by ESI-MS/MS: a new tool for the diagnosis of peroxisomal biogenesis disorders.
Topics: Carnitine; Female; Humans; Infant; Infant, Newborn; Male; Peroxisomal Disorders; Refsum Disease; Reproducibility of Results; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry; Zellweger Syndrome | 2008 |
Combined extraction of acyl carnitines and 26:0 lysophosphatidylcholine from dried blood spots: prospective newborn screening for X-linked adrenoleukodystrophy.
Topics: Adrenoleukodystrophy; Carnitine; Chromatography, Liquid; Dried Blood Spot Testing; Humans; Infant, Newborn; Lysophosphatidylcholines; Mass Spectrometry; Molecular Diagnostic Techniques; Neonatal Screening; Peroxisomal Disorders; Peroxisomes | 2012 |
Characteristic acylcarnitine profiles in inherited defects of peroxisome biogenesis: a novel tool for screening diagnosis using tandem mass spectrometry.
Topics: Carnitine; Gas Chromatography-Mass Spectrometry; Humans; Mass Spectrometry; Peroxisomal Disorders; Peroxisomes | 2003 |
Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysis.
Topics: Carnitine; Cells, Cultured; Fatty Acids; Fibroblasts; Humans; Oxidation-Reduction; Peroxisomal Disorders; Phytanic Acid | 1998 |