s-adenosylmethionine has been researched along with Nervous System Diseases in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (17.65) | 18.7374 |
| 1990's | 3 (17.65) | 18.2507 |
| 2000's | 4 (23.53) | 29.6817 |
| 2010's | 6 (35.29) | 24.3611 |
| 2020's | 1 (5.88) | 2.80 |
| Authors | Studies |
|---|---|
| Adam, T; Chrastina, P; Farolfi, M; Foltenová, H; Friedecký, D; Hanák, P; Honzík, T; Hrubá, E; Ješina, P; Kousal, B; Kožich, V; Pavlíková, M; Rücklová, K; Smolka, V; Vlášková, H; Zeman, J | 1 |
| Ask, S; Gustafsson, J; Haglind, CB; Nordenström, A; Stenlid, MH; von Döbeln, U | 1 |
| Hiramatsu, Y; Izumi, Y; Kaji, R; Matsui, N; Miyazaki, Y; Nodera, H; Takashima, H; Yamamoto, Y | 1 |
| Borum, PR; Jones, LL; McDonald, DA | 1 |
| Chang, YS; Jin, DK; Ki, CS; Kim, SR; Lee, SY; Park, HD; Park, WS | 1 |
| Bottiglieri, T; Brown, RP; Carpenter, LL; Gerbarg, P; Lavretsky, H; Massoumi, L; Mischoulon, D; Muskin, PR; Sharma, A | 1 |
| Kido, J; Kitajima, M; Matsumoto, S; Mitsubuchi, H; Momosaki, K; Nakamura, K; Sawada, T; Suzuki, Y; Uetani, H | 1 |
| Blümcke, I; Kobow, K | 1 |
| Bottiglieri, T | 1 |
| Carmel, R; James, SJ; Melnyk, S | 1 |
| Bottiglieri, T; Hyland, K | 1 |
| Metz, J | 1 |
| Scott, JM; Weir, DG | 1 |
| Capdevila, A; Jenden, DJ; Levy, HL; Mudd, SH; Roch, M; Wagner, C | 1 |
| Carney, MW | 1 |
| Blanchflower, J; Keating, S; Kennedy, DG; Kennedy, S; McPartlin, J; Molloy, A; Rice, D; Scott, JM; Weir, DG | 1 |
8 review(s) available for s-adenosylmethionine and Nervous System Diseases
| Article | Year |
|---|---|
Acylcarnitines: role in brain.
Topics: Acetylcarnitine; Animals; Antioxidants; Brain; Carnitine; Energy Metabolism; Fatty Acids; Nerve Growth Factor; Nervous System Diseases; Neuroprotective Agents | 2010 |
S-Adenosylmethionine (SAMe) for Neuropsychiatric Disorders: A Clinician-Oriented Review of Research.
Topics: Humans; Mental Disorders; Nervous System Diseases; S-Adenosylmethionine | 2017 |
The emerging role of DNA methylation in epileptogenesis.
Topics: Animals; DNA Methylation; Epigenesis, Genetic; Epigenomics; Epilepsy; Humans; Nervous System Diseases; S-Adenosylmethionine | 2012 |
S-Adenosyl-L-methionine (SAMe): from the bench to the bedside--molecular basis of a pleiotrophic molecule.
Topics: Animals; Depression; Diffusion of Innovation; Humans; Liver Diseases; Methylation; Nervous System Diseases; Osteoarthritis; S-Adenosylmethionine; Tissue Distribution | 2002 |
Nitrous oxide, vitamin B12 deficiency and the methyl folate trap.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Megaloblastic; Animals; Humans; Liver; Macaca fascicularis; Methionine; Methylmalonyl-CoA Mutase; Nervous System Diseases; Nitrous Oxide; Rats; S-Adenosylhomocysteine; S-Adenosylmethionine; Tetrahydrofolates; Vitamin B 12 Deficiency | 1982 |
S-adenosylmethionine levels in psychiatric and neurological disorders: a review.
Topics: Administration, Oral; Adolescent; Adult; Age Factors; Aged; AIDS Dementia Complex; Alzheimer Disease; Brain; Catecholamines; Child; Child, Preschool; Depressive Disorder; DNA; Female; Humans; Injections, Intravenous; Liver; Male; Metabolic Diseases; Methylation; Middle Aged; Nervous System Diseases; Phospholipids; RNA; S-Adenosylmethionine; Spinal Cord Diseases | 1994 |
Brain function in the elderly: role of vitamin B12 and folate.
Topics: Aged; DNA; Folic Acid; Folic Acid Deficiency; Humans; Methylation; Nervous System Diseases; S-Adenosylmethionine; Vitamin B 12; Vitamin B 12 Deficiency | 1999 |
Neuropharmacology of S-adenosyl methionine.
Topics: Animals; Antidepressive Agents; Biogenic Amines; Brain; Dementia; Depressive Disorder; Epilepsy; Folic Acid; Humans; Hydroxyindoleacetic Acid; Mental Disorders; Methionine Adenosyltransferase; Methylation; Nervous System Diseases; Phospholipids; Proteins; Rats; S-Adenosylmethionine; Schizophrenia; Synapses; Synaptic Transmission | 1986 |
9 other study(ies) available for s-adenosylmethionine and Nervous System Diseases
| Article | Year |
|---|---|
Impact of Newborn Screening and Early Dietary Management on Clinical Outcome of Patients with Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency and Medium Chain Acyl-CoA Dehydrogenase Deficiency-A Retrospective Nationwide Study.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase; Cardiomyopathies; Carnitine; Child; Child, Preschool; Czech Republic; Female; Humans; Incidence; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Metabolism, Inborn Errors; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Neonatal Screening; Nervous System Diseases; Outcome Assessment, Health Care; Retrospective Studies; Rhabdomyolysis; Severity of Illness Index | 2021 |
Increased and early lipolysis in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency during fast.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Age Factors; Biomarkers; Blood Glucose; Calorimetry, Indirect; Cardiomyopathies; Carnitine; Child; Child, Preschool; Energy Metabolism; Fasting; Female; Glycerol; Humans; Hyperglycemia; Isotope Labeling; Lipid Metabolism, Inborn Errors; Lipolysis; Male; Microdialysis; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Postprandial Period; Rhabdomyolysis; Time Factors | 2015 |
Mitochondrial trifunctional protein deficiency: an adult patient with similar progress to Charcot-Marie-Tooth disease.
Topics: Biomarkers; Cardiomyopathies; Carnitine; Charcot-Marie-Tooth Disease; Diagnosis, Differential; Disease Progression; Genetic Testing; Humans; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Recurrence; Rhabdomyolysis | 2017 |
Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Carnitine; DNA Mutational Analysis; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondria; Mitochondrial Myopathies; Mitochondrial Proteins; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Multienzyme Complexes; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Republic of Korea; Retinitis Pigmentosa; Rhabdomyolysis | 2009 |
Neonatal methionine adenosyltransferase I/III deficiency with abnormal signal intensity in the central tegmental tract.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Demyelinating Diseases; Glycine N-Methyltransferase; Humans; Infant; Infant, Newborn; Male; Methionine; Methionine Adenosyltransferase; Neonatal Screening; Nervous System Diseases; Pontine Tegmentum; S-Adenosylmethionine | 2019 |
Cobalamin deficiency with and without neurologic abnormalities: differences in homocysteine and methionine metabolism.
Topics: Anemia; Anemia, Pernicious; Cysteine; Dipeptides; Folic Acid; Glutathione; Homocysteine; Humans; Memory Disorders; Methionine; Movement Disorders; Nervous System Diseases; Retrospective Studies; S-Adenosylmethionine; Sensation Disorders; Vitamin B 12; Vitamin B 12 Deficiency | 2003 |
Pathogenesis of cobalamin neuropathy: deficiency of nervous system S-adenosylmethionine?
Topics: Child, Preschool; Folic Acid; Folic Acid Deficiency; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Nervous System Diseases; S-Adenosylmethionine; Vitamin B 12; Vitamin B 12 Deficiency | 1993 |
Isolated hypermethioninemia: measurements of S-adenosylmethionine and choline.
Topics: Choline; Humans; Isoenzymes; Methionine; Methionine Adenosyltransferase; Nervous System Diseases; S-Adenosylmethionine | 2000 |
Methylation deficiency causes vitamin B12-associated neuropathy in the pig.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Animals; Homocysteine; Methylation; Nervous System Diseases; Nitrous Oxide; S-Adenosylhomocysteine; S-Adenosylmethionine; Spinal Cord; Swine; Vitamin B 12 | 1988 |