salicylic acid has been researched along with Creutzfeldt-Jakob Syndrome in 2 studies
Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).
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 | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Honda, H | 1 |
| Mori, S | 1 |
| Watanabe, A | 1 |
| Sasagasako, N | 1 |
| Sadashima, S | 1 |
| Đồng, T | 1 |
| Satoh, K | 1 |
| Nishida, N | 1 |
| Iwaki, T | 1 |
| Ferree, TC | 1 |
| Luu, P | 1 |
| Russell, GS | 1 |
| Tucker, DM | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| A Pilot Study of Seizure Detection in Neonates Using Multimodal Temporary Epidermal Electronics[NCT02451618] | 13 participants (Actual) | Observational | 2015-01-27 | Terminated (stopped due to Trial was discontinued due to inadequate signal from study eeg leads.) | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
2 other studies available for salicylic acid and Creutzfeldt-Jakob Syndrome
| Article | Year |
|---|---|
Abnormal prion protein deposits with high seeding activities in the skeletal muscle, femoral nerve, and scalp of an autopsied case of sporadic Creutzfeldt-Jakob disease.
Topics: Aged; Autopsy; Cerebral Cortex; Creutzfeldt-Jakob Syndrome; Female; Femoral Nerve; Humans; Muscle, S | 2021 |
Scalp electrode impedance, infection risk, and EEG data quality.
Topics: Artifacts; Creutzfeldt-Jakob Syndrome; Cross Infection; Electric Impedance; Electrodes; Electroencep | 2001 |