s-adenosylmethionine has been researched along with Recrudescence in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (12.50) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 4 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Phowthongkum, P; Shotelersuk, V; Suphapeetiporn, K | 1 |
| Christensen, E; Duno, M; Olesen, JH; Rafiq, J; Risom, L; Vissing, CR; Vissing, J; Wibrand, F | 1 |
| Hiramatsu, Y; Izumi, Y; Kaji, R; Matsui, N; Miyazaki, Y; Nodera, H; Takashima, H; Yamamoto, Y | 1 |
| Jumma, O; Ogundare, O; Turnbull, DM; Woywodt, A | 1 |
| Arrowsmith, CH; Brown, PJ; Dong, A; Duan, S; He, H; Li, F; Schapira, M; Seitova, A; Senisterra, G; Vedadi, M; Wu, H; Zeng, H | 1 |
| Brown, AT; Cruz, C; Drouilhet, J; Eidt, J; Moursi, MM; Mukunyadzi, P; Poirier, LA; Southern, F; Wang, YF; Williams, DK | 1 |
| Ghent, CN | 1 |
| Ahnen, D; Everson, GT; Harper, PC; Krawitt, EL | 1 |
8 other study(ies) available for s-adenosylmethionine and Recrudescence
| Article | Year |
|---|---|
Carnitine palmitoyl transferase 1A deficiency in an adult with recurrent severe steato hepatitis aggravated by high pathologic or physiologic demands: A roller-coaster for internists.
Topics: Adult; Anti-Bacterial Agents; Carnitine; Carnitine O-Palmitoyltransferase; Escherichia coli Infections; Humans; Hypoglycemia; Lipid Metabolism, Inborn Errors; Liver; Male; Mutation, Missense; Non-alcoholic Fatty Liver Disease; Recurrence; Severity of Illness Index | 2019 |
Recurrent myoglobinuria and deranged acylcarnitines due to a mutation in the mtDNA MT-CO2 gene.
Topics: Adult; Carnitine; DNA, Mitochondrial; Electron Transport Complex IV; Humans; Male; Mutation; Myoglobinuria; Recurrence | 2013 |
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 |
Searching for the needle in the Haystacks.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Age of Onset; Biopsy; Carnitine; Creatine Kinase; Creatinine; Histocytochemistry; Humans; Male; Middle Aged; Mitochondrial Myopathies; Prognosis; Rare Diseases; Recurrence; Rhabdomyolysis; Walking | 2009 |
Structure of the catalytic domain of EZH2 reveals conformational plasticity in cofactor and substrate binding sites and explains oncogenic mutations.
Topics: Amino Acid Sequence; Animals; Carcinogenesis; Catalytic Domain; Coenzymes; Crystallography, X-Ray; Enhancer of Zeste Homolog 2 Protein; Enzyme Activation; Humans; Lymphoma; Mice; Models, Molecular; Molecular Sequence Data; Mutation; Polycomb Repressive Complex 2; Protein Binding; Recurrence; S-Adenosylmethionine | 2013 |
Increasing levels of dietary homocystine with carotid endarterectomy produced proportionate increases in plasma homocysteine and intimal hyperplasia.
Topics: Animals; Carotid Arteries; Cystathionine beta-Synthase; Endarterectomy, Carotid; Homocysteine; Homocystine; Hyperplasia; Liver; Male; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Rats; Rats, Sprague-Dawley; Recurrence; S-Adenosylhomocysteine; S-Adenosylmethionine; Tunica Intima | 2001 |
Benign recurrent intrahepatic cholestasis: failure of S-adenosylmethionine therapy.
Topics: Cholestasis, Intrahepatic; Drug Evaluation; Female; Humans; Male; Recurrence; S-Adenosylmethionine | 1990 |
Benign recurrent intrahepatic cholestasis: treatment with S-adenosylmethionine.
Topics: Bile Acids and Salts; Bilirubin; Cholestasis, Intrahepatic; Female; Humans; Liver; Liver Function Tests; Male; Recurrence; S-Adenosylmethionine | 1989 |