s-adenosylmethionine has been researched along with Acquired Metabolic Diseases, Brain 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 | 2 (33.33) | 29.6817 |
| 2010's | 4 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| da Silva, JM; de Moura Coelho, D; Deon, M; Ribas, GS; Sitta, A; Vargas, CR; Wajner, M | 1 |
| Acquaviva-Bourdain, C; Brivet, M; Eymard, B; Jardel, C; Laforêt, P; Lombès, A; Maillart, E; Rigal, O; Vianey-Saban, C | 1 |
| Espinoza, L; Holden, KR; Pollard, LM; Schroer, RJ; Spector, EB; Williams, NR; Wood, TC | 1 |
| Cowan, TM; Le, A; Moore, T | 1 |
| Champion, MP; Dalton, RN; Turner, C; Wraige, E | 1 |
| Andersen, O; Andresen, BS; Beresford, MW; Cornelius, N; Dean, JC; Frerman, FE; Gregersen, N; Holme, E; Merinero, B; Miedzybrodzka, ZH; Morris, AA; Oldfors, A; Olpin, SE; Olsen, RK; Pourfarzam, M; Turnbull, DM | 1 |
6 other study(ies) available for s-adenosylmethionine and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
Selective Screening of Fatty Acids Oxidation Defects and Organic Acidemias by Liquid Chromatography/tandem Mass Spectrometry Acylcarnitine Analysis in Brazilian Patients.
Topics: Acyl-CoA Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Brazil; Carnitine; Child, Preschool; Chromatography, Liquid; Fatty Acids; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mass Screening; Oxidation-Reduction; Prevalence; Tandem Mass Spectrometry; Young Adult | 2018 |
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis].
Topics: Acyl-CoA Dehydrogenases; Adult; Biopsy; Brain Diseases, Metabolic; Carnitine; Coloring Agents; DNA Mutational Analysis; Electron Transport; Electron-Transferring Flavoproteins; Female; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Middle Aged; Muscle Weakness; Muscle, Skeletal; Riboflavin; Tandem Mass Spectrometry; Young Adult | 2010 |
Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency.
Topics: Brain Diseases, Metabolic; Carnitine; Child; Child, Preschool; Developmental Disabilities; Female; Humans; Male; Mass Screening; Metabolic Diseases; Multiple Acyl Coenzyme A Dehydrogenase Deficiency | 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 |
Fat oxidation defect presenting with overwhelming ketonuria.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Brain Diseases, Metabolic; Carnitine; Female; Humans; Hypoglycemia; Infant; Ketone Bodies; Oxidation-Reduction | 2002 |
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Brain Diseases, Metabolic; Carnitine; Child; Child, Preschool; Electron Transport; Electron-Transferring Flavoproteins; Fatty Acids; Female; Humans; Iron-Sulfur Proteins; Male; Metabolism, Inborn Errors; Mitochondria, Muscle; Mitochondrial Myopathies; Muscle, Skeletal; Mutation; Oxidation-Reduction; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin | 2007 |