Creutzfeldt-Jakob Syndrome
"Creutzfeldt-Jakob Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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))
| Descriptor ID |
D007562
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| MeSH Number(s) |
C10.228.140.380.165 C10.228.228.800.230 F03.615.400.300
|
| Concept/Terms |
Creutzfeldt-Jakob Syndrome- Creutzfeldt-Jakob Syndrome
- Creutzfeldt Jakob Syndrome
- Syndrome, Creutzfeldt-Jakob
- Creutzfeldt-Jakob Disease
- Creutzfeldt Jakob Disease
- Disease, Creutzfeldt-Jakob
- Jakob-Creutzfeldt Disease
- Disease, Jakob-Creutzfeldt
- Jakob Creutzfeldt Disease
- CJD (Creutzfeldt-Jakob Disease)
- CJD (Creutzfeldt Jakob Disease)
- Spongiform Encephalopathy, Subacute
- Encephalopathies, Subacute Spongiform
- Encephalopathy, Subacute Spongiform
- Spongiform Encephalopathies, Subacute
- Subacute Spongiform Encephalopathies
- Subacute Spongiform Encephalopathy
- Creutzfeldt Jacob Disease
- Disease, Creutzfeldt Jacob
- Jacob Disease, Creutzfeldt
- Jakob-Creutzfeldt Syndrome
- Jakob Creutzfeldt Syndrome
- Syndrome, Jakob-Creutzfeldt
Creutzfeldt-Jakob Disease, Familial- Creutzfeldt-Jakob Disease, Familial
- Creutzfeldt Jakob Disease, Familial
- Creutzfeldt-Jakob Diseases, Familial
- Disease, Familial Creutzfeldt-Jakob
- Familial Creutzfeldt-Jakob Diseases
- Familial Creutzfeldt-Jakob Disease
- Familial Creutzfeldt Jakob Disease
New Variant Creutzfeldt-Jakob Disease- New Variant Creutzfeldt-Jakob Disease
- New Variant Creutzfeldt Jakob Disease
- Creutzfeldt-Jakob Disease, Variant
- Creutzfeldt Jakob Disease, Variant
- Creutzfeldt-Jakob Disease, New Variant
- Creutzfeldt Jakob Disease, New Variant
- Variant Creutzfeldt-Jakob Disease
- Variant Creutzfeldt Jakob Disease
- V-CJD (Variant-Creutzfeldt-Jakob Disease)
- V CJD (Variant Creutzfeldt Jakob Disease)
|
Below are MeSH descriptors whose meaning is more general than "Creutzfeldt-Jakob Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Creutzfeldt-Jakob Syndrome".
This graph shows the total number of publications written about "Creutzfeldt-Jakob Syndrome" by people in this website by year, and whether "Creutzfeldt-Jakob Syndrome" was a major or minor topic of these publications.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 2 | 2 | 4 |
| 1996 | 1 | 2 | 3 |
| 1997 | 3 | 1 | 4 |
| 1998 | 0 | 1 | 1 |
| 1999 | 0 | 1 | 1 |
| 2000 | 0 | 2 | 2 |
| 2002 | 1 | 1 | 2 |
| 2003 | 6 | 2 | 8 |
| 2004 | 4 | 1 | 5 |
| 2005 | 7 | 0 | 7 |
| 2006 | 5 | 0 | 5 |
| 2007 | 3 | 2 | 5 |
| 2008 | 3 | 0 | 3 |
| 2009 | 4 | 2 | 6 |
| 2010 | 2 | 1 | 3 |
| 2011 | 2 | 0 | 2 |
| 2012 | 3 | 0 | 3 |
| 2013 | 3 | 0 | 3 |
| 2014 | 4 | 3 | 7 |
| 2015 | 3 | 2 | 5 |
| 2016 | 5 | 1 | 6 |
| 2017 | 1 | 2 | 3 |
| 2018 | 1 | 2 | 3 |
| 2019 | 4 | 0 | 4 |
| 2020 | 6 | 0 | 6 |
| 2021 | 4 | 1 | 5 |
| 2022 | 8 | 0 | 8 |
| 2023 | 1 | 0 | 1 |
| 2024 | 2 | 1 | 3 |
Below are the most recent publications written about "Creutzfeldt-Jakob Syndrome" by people in Profiles.
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Genome wide association study of clinical duration and age at onset of sporadic CJD. PLoS One. 2024; 19(7):e0304528.
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Insufficient evidence for an association between iatrogenic Alzheimer's disease and cadaveric pituitary-derived growth hormone. Alzheimers Dement. 2024 Oct; 20(10):7399-7402.
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Change in Epidemiology of Creutzfeldt-Jakob Disease in the US, 2007-2020. JAMA Neurol. 2024 Feb 01; 81(2):195-197.
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PRNP expression predicts imaging findings in sporadic Creutzfeldt-Jakob disease. Ann Clin Transl Neurol. 2023 04; 10(4):536-552.
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Right Brain: The Purple Scarf and the Cortical Ribbon. Neurology. 2023 03 14; 100(11):537-539.
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Developing neuropalliative care for sporadic Creutzfeldt-Jakob Disease. Prion. 2022 12; 16(1):23-39.
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Caregiver Experiences Navigating the Diagnostic Journey in a Rapidly Progressing Dementia. J Geriatr Psychiatry Neurol. 2023 07; 36(4):282-294.
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Prions induce an early Arc response and a subsequent reduction in mGluR5 in the hippocampus. Neurobiol Dis. 2022 10 01; 172:105834.
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Minimal change prion retinopathy: Morphometric comparison of retinal and brain prion deposits in Creutzfeldt-Jakob disease. Exp Eye Res. 2022 09; 222:109172.
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Default Mode Network quantitative diffusion and resting-state functional magnetic resonance imaging correlates in sporadic Creutzfeldt-Jakob disease. Hum Brain Mapp. 2022 09; 43(13):4158-4173.