adrenic acid has been researched along with Huntington Disease in 1 studies
adrenic acid: RN given refers to cpd without isomeric designation
Huntington Disease: A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Reichert, CO | 1 |
| de Freitas, FA | 1 |
| Sampaio-Silva, J | 1 |
| Rokita-Rosa, L | 1 |
| Barros, PL | 1 |
| Levy, D | 1 |
| Bydlowski, SP | 1 |
1 review available for adrenic acid and Huntington Disease
| Article | Year |
|---|---|
Ferroptosis Mechanisms Involved in Neurodegenerative Diseases.
Topics: Alzheimer Disease; Arachidonate 15-Lipoxygenase; Arachidonic Acid; Brain; Cell Membrane; Fatty Acids | 2020 |