creatine has been researched along with Creutzfeldt-Jakob Syndrome in 5 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))
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kim, JH | 1 |
| Choi, BS | 1 |
| Jung, C | 1 |
| Chang, Y | 1 |
| Kim, S | 1 |
| Galanaud, D | 2 |
| Dormont, D | 1 |
| Grabli, D | 1 |
| Charles, P | 1 |
| Hauw, JJ | 1 |
| Lubetzki, C | 1 |
| Brandel, JP | 1 |
| Marsault, C | 1 |
| Cozzone, PJ | 1 |
| Pandya, HG | 1 |
| Coley, SC | 1 |
| Wilkinson, ID | 1 |
| Griffiths, PD | 1 |
| Oppenheim, C | 1 |
| Zuber, M | 1 |
| Detilleux, M | 1 |
| Bolgert, F | 1 |
| Mas, JL | 1 |
| Chiras, J | 1 |
| Meder, JF | 1 |
| Cordery, RJ | 1 |
| MacManus, D | 1 |
| Godbolt, A | 1 |
| Rossor, MN | 1 |
| Waldman, AD | 1 |
5 other studies available for creatine and Creutzfeldt-Jakob Syndrome
| Article | Year |
|---|---|
Diffusion-weighted imaging and magnetic resonance spectroscopy of sporadic Creutzfeldt-Jakob disease: correlation with clinical course.
Topics: Aged; Aspartic Acid; Biomarkers; Brain; Choline; Creatine; Creutzfeldt-Jakob Syndrome; Diffusion Mag | 2011 |
MR spectroscopic pulvinar sign in a case of variant Creutzfeldt-Jakob disease.
Topics: Adult; Aspartic Acid; Biopsy; Case-Control Studies; Choline; Creatine; Creutzfeldt-Jakob Syndrome; F | 2002 |
Magnetic resonance spectroscopic abnormalities in sporadic and variant Creutzfeldt-Jakob disease.
Topics: Adult; Aged; Aspartic Acid; Basal Ganglia; Creatine; Creutzfeldt-Jakob Syndrome; Fatal Outcome; Fema | 2003 |
Spectroscopy and serial diffusion MR findings in hGH-Creutzfeldt-Jakob disease.
Topics: Adult; Aspartic Acid; Creatine; Creutzfeldt-Jakob Syndrome; Diffusion Magnetic Resonance Imaging; Hu | 2004 |
Short TE quantitative proton magnetic resonance spectroscopy in variant Creutzfeldt-Jakob disease.
Topics: Adult; Aspartic Acid; Case-Control Studies; Choline; Creatine; Creutzfeldt-Jakob Syndrome; Female; G | 2006 |