s-adenosylmethionine has been researched along with Fatty Liver with Encephalopathy in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bekhof, J; de Koning, TJ; Derks, TG; Heiner Fokkema, MR; Koolhaas, GD; Schielen, PC; van Rijt, WJ; van Spronsen, FJ; Visser, G | 1 |
| Hoffmann, GF; Koelker, S; Morath, MA; Okun, JG; Sauer, SW | 1 |
| Fukao, T; Hasegawa, Y; Hori, T; Kobayashi, H; Kondo, N; Takayanagi, M; Teramoto, T; Yamaguchi, S; Yasuno, T | 1 |
| Armstrong, DL; Scaglia, F; Scheuerle, AE; Sweetman, L; Towbin, JA; Wong, LJ | 1 |
| Hillman, SL; Matern, D; Mayatepek, E; Millington, DS; Strauss, AW; Trefz, FK | 1 |
1 review(s) available for s-adenosylmethionine and Fatty Liver with Encephalopathy
| Article | Year |
|---|---|
Inborn Errors of Metabolism That Cause Sudden Infant Death: A Systematic Review with Implications for Population Neonatal Screening Programmes.
Topics: Amino Acids; Autopsy; Carnitine; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Neonatal Screening; Reye Syndrome; Sudden Infant Death | 2016 |
4 other study(ies) available for s-adenosylmethionine and Fatty Liver with Encephalopathy
| Article | Year |
|---|---|
Impact of short- and medium-chain organic acids, acylcarnitines, and acyl-CoAs on mitochondrial energy metabolism.
Topics: Acids; Acyl Coenzyme A; Animals; Carnitine; Cattle; Electron Transport Complex III; Energy Metabolism; Humans; Mitochondria; Reye Syndrome | 2008 |
Carnitine palmitoyltransferase 2 deficiency: the time-course of blood and urinary acylcarnitine levels during initial L-carnitine supplementation.
Topics: Acetylcarnitine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Carnitine; Carnitine O-Palmitoyltransferase; Child, Preschool; Female; Follow-Up Studies; Humans; Infant; Lipid Metabolism, Inborn Errors; Reye Syndrome; Time Factors; Treatment Outcome; Vitamin B Complex | 2010 |
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 |
Diagnosis of mitochondrial trifunctional protein deficiency in a blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Base Sequence; Cardiomyopathies; Carnitine; DNA; Female; Genetic Testing; Heterozygote; Humans; Infant, Newborn; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Male; Mass Spectrometry; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Mutation, Missense; Neonatal Screening; Nuclear Family; Reye Syndrome; Sequence Deletion | 1999 |