prednisolone has been researched along with Creutzfeldt-Jakob Syndrome in 2 studies
Prednisolone: A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
prednisolone : A glucocorticoid that is prednisone in which the oxo group at position 11 has been reduced to the corresponding beta-hydroxy group. It is a drug metabolite of prednisone.
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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kondziella, D | 1 |
| Hansen, K | 1 |
| Gonzalez, T | 1 |
| Gideon, P | 1 |
| Christiansen, I | 1 |
| Sellebjerg, F | 1 |
| Utsumiya, K | 1 |
| Arakawa, R | 1 |
| Fujimoto, S | 1 |
| Ueyama, H | 1 |
| Kumamoto, T | 1 |
2 other studies available for prednisolone and Creutzfeldt-Jakob Syndrome
| Article | Year |
|---|---|
[Anti-thyroid antibodies in two patients with subacute dementia, ataxia, and myoclonus].
Topics: Aged; Antibodies; Ataxia; Brain Diseases; Cerebrum; Creutzfeldt-Jakob Syndrome; Dementia; Diagnosis, | 2012 |
[A case of steroid-responsive encephalopathy with positive 14-3-3 protein of the cerebrospinal fluid clinically resembling Creutzfelt-Jakob disease].
Topics: 14-3-3 Proteins; Aged; Brain Diseases; Creutzfeldt-Jakob Syndrome; Diagnosis, Differential; Humans; | 2004 |