corticosterone has been researched along with Huntington Disease in 8 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)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 7 (87.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dufour, BD | 2 |
| McBride, JL | 2 |
| Mo, C | 4 |
| Renoir, T | 5 |
| Pang, TY | 3 |
| Hannan, AJ | 5 |
| Ransome, MI | 1 |
| Hill, RA | 1 |
| Du, X | 1 |
| Leang, L | 1 |
| Mustafa, T | 1 |
| Björkqvist, M | 1 |
| Petersén, A | 1 |
| Bacos, K | 1 |
| Isaacs, J | 1 |
| Norlén, P | 1 |
| Gil, J | 1 |
| Popovic, N | 1 |
| Sundler, F | 1 |
| Bates, GP | 1 |
| Tabrizi, SJ | 1 |
| Brundin, P | 1 |
| Mulder, H | 1 |
8 other studies available for corticosterone and Huntington Disease
| Article | Year |
|---|---|
Normalizing glucocorticoid levels attenuates metabolic and neuropathological symptoms in the R6/2 mouse model of huntington's disease.
Topics: Adrenalectomy; Animals; Atrophy; Body Weight; Brain; Corticosterone; Disease Models, Animal; Eating; | 2019 |
Short-term memory acquisition in female Huntington's disease mice is vulnerable to acute stress.
Topics: Animals; Cognition; Corticosterone; Exploratory Behavior; Female; Humans; Huntington Disease; Male; | 2013 |
High stress hormone levels accelerate the onset of memory deficits in male Huntington's disease mice.
Topics: Age of Onset; Animals; Brain-Derived Neurotrophic Factor; Cell Proliferation; Corticosterone; Diseas | 2014 |
Effects of chronic stress on the onset and progression of Huntington's disease in transgenic mice.
Topics: Animals; Corticosterone; Disease Models, Animal; Disease Progression; Female; Humans; Huntingtin Pro | 2014 |
Ethological endophenotypes are altered by elevated stress hormone levels in both Huntington's disease and wildtype mice.
Topics: Animals; Anti-Inflammatory Agents; Corticosterone; Disease Models, Animal; Dose-Response Relationshi | 2014 |
Corticosterone dysregulation exacerbates disease progression in the R6/2 transgenic mouse model of Huntington's disease.
Topics: Adrenalectomy; Age Factors; Animals; Anti-Inflammatory Agents; Body Weight; Corticosterone; Disease | 2016 |
Environmental enrichment rescues female-specific hyperactivity of the hypothalamic-pituitary-adrenal axis in a model of Huntington's disease.
Topics: Adrenal Glands; Adrenocorticotropic Hormone; Analysis of Variance; Animals; Corticosterone; Dexameth | 2012 |
Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease.
Topics: Adrenocorticotropic Hormone; Adult; Animals; Body Fat Distribution; Bone Density; Corticosterone; Di | 2006 |