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
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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)
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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.
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Year | Major Topic | Minor Topic | Total |
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2007 | 2 | 0 | 2 |
2011 | 1 | 0 | 1 |
2015 | 2 | 0 | 2 |
2019 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Creutzfeldt-Jakob Syndrome" by people in Profiles.
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Effects of the pathological E200K mutation on human prion protein: A computational screening and molecular dynamics approach. J Cell Biochem. 2023 02; 124(2):254-265.
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Variant Creutzfeldt-Jakob Disease Presenting as New-onset Psychosis. J Psychiatr Pract. 2019 Jan; 25(1):58-62.
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Blood transmission studies of prion infectivity in the squirrel monkey (Saimiri sciureus): the Baxter study. Transfusion. 2016 Mar; 56(3):712-21.
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Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications. Emerg Infect Dis. 2015 May; 21(5):750-9.
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Once upon a cataract surgeon. Surv Ophthalmol. 2012 Jul-Aug; 57(4):379-85.
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Alexia without agraphia in Creutzfeldt-Jakob disease. J Neurol Sci. 2007 Dec 15; 263(1-2):208-10.
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Clinical, neuropathological and immunohistochemical features of sporadic and variant forms of Creutzfeldt-Jakob disease in the squirrel monkey (Saimiri sciureus). J Gen Virol. 2007 Feb; 88(Pt 2):688-695.
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Cerebral MR and CT imaging in Creutzfeldt-Jakob disease. J Comput Assist Tomogr. 1985 Jan-Feb; 9(1):125-8.
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Epidemiologic comparisons between Creutzfeldt-Jakob disease and scrapie in France during the 12-year period 1968-1979. J Neurol Sci. 1981 Sep; 51(3):329-37.
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Jakob-Creutzfeldt disease: brief review and precautionary measures. Tex Med. 1978 Aug; 74(8):52-4.