s-adenosylmethionine has been researched along with glutarylcarnitine in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bain, MD; Baric, I; Chalmers, RA; Feyh, P; Hoffmann, GF; Jakobs, C; Jeffrey, I; Kölker, S; Okun, JG; Pourfarzam, M; Schor, DS; Wagner, L; Zschocke, J | 1 |
| Napolitano, N; Pitt, JJ; Wiley, V | 1 |
| Lai, CC; Lee, CC; Lin, WD; Tsai, FJ; Wang, CH | 1 |
| Chace, DH; De Jesús, VR; Hannon, WH; Lim, TH; Mei, JV | 1 |
| Cowan, TM; Le, A; Moore, T | 1 |
| Brose, SA; Hobert, JA; Pasquali, M | 1 |
6 other study(ies) available for s-adenosylmethionine and glutarylcarnitine
| Article | Year |
|---|---|
Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.
Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Analysis; Fatal Outcome; Gas Chromatography-Mass Spectrometry; Gene Expression; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Male; Muscle Hypotonia; N-Methylaspartate; Oxidoreductases Acting on CH-CH Group Donors; Point Mutation; Putamen; Spasm; Vigabatrin | 2003 |
Pseudo-glutarylcarnitinaemia in medium-chain acyl-CoA dehydrogenase deficiency detected by tandem mass spectrometry newborn screening.
Topics: Acetylation; Acyl-CoA Dehydrogenase; Carnitine; False Positive Reactions; Fatty Acids; Gas Chromatography-Mass Spectrometry; Humans; Infant, Newborn; Mass Spectrometry; Neonatal Screening; Oxidation-Reduction; Sensitivity and Specificity | 2004 |
Genetic and biochemical study in a patient with glutaric acidemia type I.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Male; Mutation; Oxidoreductases Acting on CH-CH Group Donors | 2004 |
Comparison of amino acids and acylcarnitines assay methods used in newborn screening assays by tandem mass spectrometry.
Topics: Amino Acids; Butanols; Carnitine; Humans; Infant, Newborn; Leucine; Metabolic Diseases; Methionine; Neonatal Screening; Palmitoylcarnitine; Phenylalanine; Quality Control; Tandem Mass Spectrometry | 2010 |
An improved LC-MS/MS method for the detection of classic and low excretor glutaric acidemia type 1.
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Carnitine; Case-Control Studies; Chromatography, Liquid; Follow-Up Studies; Glutaryl-CoA Dehydrogenase; Humans; Ions; Predictive Value of Tests; Reproducibility of Results; Tandem Mass Spectrometry | 2012 |
Quantitation of Butyrylcarnitine, Isobutyrylcarnitine, and Glutarylcarnitine in Urine Using Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS).
Topics: Carnitine; Chromatography, High Pressure Liquid; Chromatography, Liquid; Coenzyme A; Fatty Acids; Tandem Mass Spectrometry | 2022 |