phenol has been researched along with Creutzfeldt-Jakob Syndrome in 2 studies
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))
Excerpt | Relevance | Reference |
---|---|---|
" Since CJD brain samples are infectious at all stages of the prion extraction process, we set out to develop a laboratory safe method for prion purification." | 1.33 | Safe method for isolation of prion protein and diagnosis of Creutzfeldt-Jakob disease. ( Bastian, FO; Carver, LA; Dash, S; Garry, RF; McDermott, ME; Perry, AS, 2005) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bastian, FO | 1 |
McDermott, ME | 1 |
Perry, AS | 1 |
Carver, LA | 1 |
Dash, S | 1 |
Garry, RF | 1 |
Mackenzie, JM | 1 |
Fellowes, W | 1 |
2 other studies available for phenol and Creutzfeldt-Jakob Syndrome
Article | Year |
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Safe method for isolation of prion protein and diagnosis of Creutzfeldt-Jakob disease.
Topics: Blotting, Western; Brain Chemistry; Creutzfeldt-Jakob Syndrome; Glycosylation; Guanidines; Humans; P | 2005 |
Phenolized formalin fixation may obscure early histological changes of Creutzfeldt-Jakob disease.
Topics: Creutzfeldt-Jakob Syndrome; Fixatives; Formaldehyde; Histological Techniques; Humans; Phenol; Phenol | 1990 |