dan 2163 has been researched along with Huntington Disease in 2 studies
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)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Huntington's disease is a hereditary and progressive disease of the central nervous system." | 1.32 | [Frontal dysfunctions in Huntington's disease -- neuropsychology and therapy]. ( Braus, DF; Ries, S; Tost, H; Weimer, E, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Weimer, E | 1 |
| Ries, S | 1 |
| Tost, H | 1 |
| Braus, DF | 1 |
| Saft, C | 1 |
| Andrich, J | 1 |
| Kraus, PH | 1 |
| Przuntek, H | 1 |
2 other studies available for dan 2163 and Huntington Disease
| Article | Year |
|---|---|
[Frontal dysfunctions in Huntington's disease -- neuropsychology and therapy].
Topics: Adult; Amisulpride; Antipsychotic Agents; Attention; Brain; Dose-Response Relationship, Drug; Female | 2003 |
[Amisulpride in Huntington's disease].
Topics: Aged; Amisulpride; Antipsychotic Agents; Delusions; Dose-Response Relationship, Drug; Drug Administr | 2005 |