hydroxyindoleacetic acid has been researched along with Creutzfeldt-Jakob Syndrome in 3 studies
(5-hydroxyindol-3-yl)acetic acid : A member of the class of indole-3-acetic acids that is indole-3-acetic acid substituted by a hydroxy group at C-5.
Creutzfeldt-Jakob Syndrome: A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (100.00) | 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 | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Nyberg, P | 1 |
Almay, BG | 1 |
Carlsson, A | 1 |
Masters, C | 1 |
Winblad, B | 1 |
Chase, TN | 1 |
Brun, A | 1 |
Gottfries, CG | 1 |
Roos, BE | 1 |
1 review available for hydroxyindoleacetic acid and Creutzfeldt-Jakob Syndrome
Article | Year |
---|---|
Serotonergic mechanisms and extrapyramidal function in man.
Topics: 5-Hydroxytryptophan; Carbidopa; Cerebellar Diseases; Creutzfeldt-Jakob Syndrome; Down Syndrome; Extr | 1974 |
2 other studies available for hydroxyindoleacetic acid and Creutzfeldt-Jakob Syndrome
Article | Year |
---|---|
Brain monoamine abnormalities in the two types of Creutzfeldt-Jakob disease.
Topics: Aged; Brain; Brain Chemistry; Creutzfeldt-Jakob Syndrome; Dopamine; Female; Humans; Hydroxyindoleace | 1982 |
Studies of the monoamine metabolism in the central nervous system in Jakob-Creutzfeldt disease.
Topics: Aged; Brain; Central Nervous System; Central Nervous System Diseases; Creutzfeldt-Jakob Syndrome; Do | 1971 |