isomethyleugenol has been researched along with Dyskinesia Syndromes in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (71.43) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cheillan, D; Dessein, AF; Dobbelaere, D; Fontaine, M; Joncquel-Chevalier Curt, M; Mention-Mulliez, K; Porchet, N; Soto-Ares, G; Vamecq, J; Voicu, PM | 1 |
| ERNST, AM | 1 |
| Dill, RE; Dorris, RL; Furgeson, MD | 1 |
| Avidano, KM; Driscoll, DJ; Glenn, CC; Nicholls, RD; Waters, MF; Williams, CA; Zori, RT | 1 |
| Chase, TN; Woods, AC | 1 |
| Bohuon, C; Comoy, E; Lhermitte, F; Rosa, A | 1 |
| Radouco-Thomas, S | 1 |
1 review(s) available for isomethyleugenol and Dyskinesia Syndromes
| Article | Year |
|---|---|
Creatine biosynthesis and transport in health and disease.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; AMP-Activated Protein Kinases; Animals; Biological Transport, Active; Brain Diseases, Metabolic, Inborn; Creatine; Developmental Disabilities; Energy Metabolism; Guanidinoacetate N-Methyltransferase; Gyrate Atrophy; Humans; Hyperammonemia; Intellectual Disability; Language Development Disorders; Mental Retardation, X-Linked; Methylation; Mitochondrial Membrane Transport Proteins; Movement Disorders; Mutation; Nerve Tissue Proteins; Ornithine; Plasma Membrane Neurotransmitter Transport Proteins; Prenatal Diagnosis; S-Adenosylmethionine; Speech Disorders; Urea Cycle Disorders, Inborn | 2015 |
6 other study(ies) available for isomethyleugenol and Dyskinesia Syndromes
| Article | Year |
|---|---|
Phenomena of the hypokinetic rigid type caused by o-methylation of dopamine in the para-position.
Topics: Dihydroxyphenylalanine; Dopamine; Humans; Methylation; Movement Disorders | 1962 |
Importance of O-methylation in dopamine-induced motor and behavioral phenomena.
Topics: Animals; Behavior, Animal; Corpus Striatum; Dopamine; Drug Combinations; Humans; Hydrazines; Male; Methylation; Motor Activity; Movement Disorders; Rats; Reaction Time; Stereotyped Behavior; Tremor; Tropolone; Tyramine | 1976 |
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
Topics: Blotting, Southern; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 15; DNA; DNA Probes; Female; Humans; Intellectual Disability; Male; Methylation; Movement Disorders; Parents; Prader-Willi Syndrome; Sex Factors; Syndrome | 1992 |
M.I.F.: effect on levodopa dyskinesias in man.
Topics: Antiparkinson Agents; Carbidopa; Carboxy-Lyases; Decarboxylation; Dihydroxyphenylalanine; Dose-Response Relationship, Drug; Humans; Melanocyte-Stimulating Hormones; Methylation; Movement Disorders; Parkinson Disease | 1973 |
[Abnormal movements induced by L-Dopa and dopamine metabolism disorders].
Topics: Benzoates; Dihydroxyphenylalanine; Dopamine; Electrocoagulation; Female; Homovanillic Acid; Humans; Methylation; Middle Aged; Movement Disorders; Parkinson Disease | 1973 |
[Extrapyramidal syndrome in animal experiments: rôle of calcium and o-methylated derivatives].
Topics: Animals; Calcium; Calcium Metabolism Disorders; Depression, Chemical; Dihydroxyphenylalanine; Dopamine; Extrapyramidal Tracts; Guinea Pigs; Hydrogen-Ion Concentration; Methylation; Movement Disorders; Norepinephrine; Parkinson Disease; Pyrogallol; Rats; Reserpine; Serotonin Antagonists; Stimulation, Chemical; Synapses; Tranylcypromine | 1970 |